Natural Products: A Laboratory Guide

NATURAL PRODUCTS
A Laboratory Guide
Second Edition
Raphael Ikan
Department of Organic Chemistry
The Hebrew University of Jerusalem
Jerusalem, Israel
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Library of Congress Cataloging-in-Publication Data
Ikan, Raphael, date

Natural products : a laboratory guide / Raphael Ikan. -- 2nd ed.
p. cm.
Includes index.
ISBN 0-12-370551-7
1. Biochemistry-Laboratory manuals. I. Title.
QD415.5.I4 1991
547'.0028-dc20 91-12738
CIP
PRINTED IN THE UNITED STATES OF AMERICA

91 92 93 94 9 8 7 6 5 4 3 2 1
To my wife Yael
and our four favorite natural products
Amir am, Ariel, Arnon, and Eliana
PREFACE TO THE
SECOND EDITION
In the twenty-five years since the publication of the first edition, natural product re-
search technology has advanced incredibly through the fields of chemistry, food sci-
ence, geochemistry, materials science, and life sciences. Comparisons of these
compounds in microorganisms, algae, animals, higher plants, and marine inverte-
brates are now documented. With the advent of such techniques as Raman spectros-
copy, magic-angle spinning spectroscopy, high-resolution electron microscopy, x-ray
crystallography, and chromatographic methods, separation of positional and regio-
isomers, sterioisomers, and even isotopic isomers are now possible.
This new edition has been updated to include the following: The use of biomarkers
(organic compounds in the geospherical record with carbon skeletons) reflecting the
upsurge in geoporphyrin research primarily due to MS, yeast RNA nucleic acid stud-
ies; reversed-phase HPLC of amino acids; brewing industry applications (HPLC eval-
uation of carotenoids in orange juice and of "debittered" citrus); HPTLC of
carbohydrates; synthesis of a sweetening agent from citrus peels, synthesis and deg-
radation of alkaloids and of sterols, GC/MS uses with sterols, petroleum products,
and aromatic constituents of wine and grape juice, flash chromatography of essential
oils, optical purity of enantiomers affecting flavors, fragrances, and pheromones, as
13
well as studies of lattice inclusion compounds Ή - and C-NMR, MS, IR, and UV
data are presented for most natural products.
Used for twenty-five years in natural products organic chemistry courses, the suc-
cessful first edition has been updated and improved to meet the needs of current
research.
I wish to express my thanks to the following publishers and societies for their kind
permission to reproduce tables, figures, and procedures: Academic Press, Association
of Official Agricultural Chemists, Elsevier Publishing Company, John Witey and
Sons, Macmillan and Company, Methuen and Company, Naturwissenschaften Edi-
tors, Pergamon Press, Perkin Elmer Company, The American Chemical Society, The
American Society of Biological Chemists, The Biochemical Society (London), The
xi
xii Preface to the Second Edition
Royal Chemical Society (London), Varian Associates, Verlag Chemie, and Springer
Verlag.
Sincere thanks are due to my colleagues, Drs. Bernard Crammer, Vera Weinstein
and Jeana Gross (Institute of Chemistry, Hebrew University, Jerusalem), and Dr.
Uzi Ravid (Department of Natural Products, Agricultural Research Organization,
Ne we Ya'ar).
PREFACE TO THE
FIRST EDITION
The syllabus of the practical course in organic chemistry at most universities

mainly covers the synthesis of aliphatic, alicyclic, aromatic, and heterocyclic com-
pounds, as well as qualitative and quantitative analysis. For some time, the De-
partment of Organic Chemistry at the Hebrew University, Jerusalem, has felt that
it would be of value to the students, either at the undergraduate or graduate level,
to take a comprehensive course in natural products, so as to become acquainted
with the methods of isolating these products from plant and animal matter and
of determining their structures by physical methods, degraduation and, finally,
synthesis.
The study of natural products has always been the starting point of the discipline
of chemistry in every country of the globe, and, in view of the importance of these
organic compounds in agriculture, medicine, and industry, every student of chemistry
today feels the need to acquire further knowledge in this field.
In 1961, I organized a course on the subject and prepared a manual (in Hebrew)
entitled "Natural Products Laboratory Guide." In the subsequent years I have repeat-
edly given this course to graduate students specializing in organic and physical chem-
istry, biochemistry, biology, and agricultural chemistry, as well as to undergraduate
students (in the last trimester of their third year of studies).
Over the seven years during which I conducted this course, I have found that it was
received enthusiastically by the participants at all levels. It stimulated many of them
to choose the field of natural products as the theme for their M.Sc. and Ph.D. theses.
Visiting scientists from abroad who have become acquainted with the course and
its methods were favorably impressed and encouraged me to publish the manual in a
form suitable for wide distribution.
The book in its present form includes the following "biogenetic" chapters:
1. Acetogenins: flavonoids, lipids, lignans, quinones.
2. Carbohydrates: mono-, oligo- and polyaccharides.
3. Isoprenoids: cartenoids, steroids, terpenoids.
4. Nitrogens compounds: alkaloids, amino acids, nucleic acids, peptides porphy-
rins, proteins, pteridines.
xiii
xiv Preface to the First Edition
Each section of these chapters includes a general introduction and methods of

isolation, degraduation, and transformation, as well as applications of chromato-
graphic procedures. The introduction to each chapter is brief and attempts only to
supply or recall knowledge in the particular field. The student, who does not always
find the time to read the relevant books or reviews, will find in this introduction the
required material in a "concentrated" form. Furthermore, at the end of each chapter
there is a list of recommended books for additional study. Typical experiments were
selected for each chapter, taking into consideration the following factors: availability
of starting materials and the performance time. Most of the procedures were tailored
to the modest facilities of the students' laboratory.
Each experiment is described under the following headings: Introduction, Refer-
ences, Recommended Reviews, Principle, Apparatus, Materials, Time, Procedure
(often including spectral data). At the end of each section appears a list of questions.
A large number of experiments are described in order to give the instructor a rea-
sonable degree of freedom.
I am deeply indebted to Professor E. D. Bergmann for his encouragement, con-
structive comments, and criticism. I thank also Professor J. Klein and Dr. J. Radell
for their helpful guidance in the first stages of this work, and Drs. Y. Lapidot and
N. de Groot for their valuable suggestions on nucleic acids.
Acknowledgments are due Mr. R. Amoils for editing the manuscript, and to Mr. Y.
Lakitchewitch for drawing the formulas. Last, but certainly not least, I wish to thank
my wife for her expert typing of the manuscript, and our parents for their interest and
encouragement.
ACETOGENINS
The compounds grouped together in this chapter are different in most chemi-
cal properties, but similar in that many of them possess an aromatic ring
bearing hydroxyl substituents. Many of these compounds possess a diversity of
physiological properties. All of these natural products appear to be biosyn-
thetically related in being derived by condensation of several molecules of
acetate. Speculation regarding biosynthesis of all such poly acetate com-
pounds may be found in several biogenetics books.
I. FLAVONOIDS
A. Introduction
The flavonoid compounds can be regarded as C 6 - C 3 - C 6 compounds, in which

each C 6 moiety is a benzene ring, the variation in the state of oxidation of
the connecting C 3 moiety determining the properties and class of each such
compound. The classes are shown below.
Flavone Flavonol
1
2 CHAPTER 1 Acetogenins
HO HO ~ 0
#
OH
-6
Flavanone Flavanonol
HO oH
HO~OH
OH ~C-CH=CH f , OH
b -
Isoflavone Chalcone
HO~O) ;=\OH
W=CH~OH
OH b
Dihydrochalcone
Dihydrochalcone Aurone
Aurone
OH OH
HO 0 HO 0
;} OH
~
I +
~ OH
OH
Anthocyanidin Catechin
OH
HO ~ 0
~I
HO
Flavan-3,4-diol
Flavonoid compounds and the related coumarins usually occur in plants

as glycosides in which one or more of the phenolic hydroxyl groups are
combined with sugar residues. The hydroxyl groups are nearly always found
in positions 5 and 7 in ring A, while ring Β commonly carries hydroxyl or
alkoxyl groups at the 4'-position, or at both 3'- and 4'-positions. Glycosides of
flavonoid compounds may bear the sugar on any of the available hydroxyl
groups.
I. Flavonoids 3
Flavonoids occur in all parts of plants, including the fruit, pollen, roots,
and heartwood. Numerous physiological activities have been attributed to
them. Thus, small quantities of flavones may act as cardiac stimulants; some
flavones, e.g., hesperidin, appear to strengthen weak capillary blood vessels;
highly hydroxylated flavones act as diuretics and as antioxidants for fats. It is
also claimed that flavones behave like auxins in stimulating the germination of
wheat seeds.
The possible function of this coloring matter in insect-pollinated flowers
and edible fruits is to make these organs more conspicuous in order to aid
seed dispersion by animals.
The fundamental method in structural studies is alkaline hydrolysis.
Thus, alkaline degradation of chrysin yields phloroglucinol, acetic acid, ben-
zoic acid, and a small amount of acetophenone.
HO 6
Chrysin
H O ^ \ OH
1 11
+ C H 3C O O H + C 6H 5C O O H + C H 3C O C 6H 5
Si
Phloroglucinol
By spectroscopic measurement it is now possible to determine the

structures of some flavonoid compounds on the basis of their spectra alone.
Color reactions also play an important role in identification of flavonoids at
the preliminary stage of analysis.
The possibility of interconversion between the various structures in this
group is of considerable importance for the structural elucidation of flavonoid
compounds. Thus, chalcones and flavanones are isomeric and readily undergo
interconversion.
Flavanone (Butin)
Flavanones may be converted into flavonols and flavones.
Flavonol
1. Flavones
In flavones, ring C is basic and forms a pyrylium salt with hydrochloric acid.
Flavone
Consequently, the carbonyl group of flavone does not react normally

with some carbonyl reagents such as hydroxylamine. However, it does react
normally with Grignard reagents. The most widespread flavone is quercetin.
OH
Fisetin
I. Flavonoids 5
Some flavones, such as primuletin and fisetin, have only one hydroxyl group
in ring A.
2. Flavanones
Flavanone has not yet been found in nature. Hydroxylated flavanones,
however, do occur in nature, either in the free form or as glycosides. In plants
they frequently coexist with the corresponding flavones, e.g., hesperidin and
diosmin in the bark of Zanthoxylum avicennae, the rhoifolin and naringin in
the peel of Citrus aurannum.
Unlike the unsaturated flavones, the saturated flavanones show reactiv-
ity of the 4-carbonyl group. The behavior of flavanones toward alkalis differs
from that of flavones; the former decompose into benzaldehyde, acetic acid,
and phenol under drastic conditions, whereas the latter yield phenol and
cinnamic acid. Dehydrogenation of flavanones, e.g., conversion of hesperitin
into diosmin, is of importance, as it makes possible the rapid identification of
a new flavanone by reference to a known flavone. The following flavanones
merit mentioning:
Hesperidin Prunin
3. Isoflavones
The isoflavones are 3-phenylchromones. At present about 35 isoflavones are
known, of which the following are examples:
Daidzein Genistein
Tlanlancuayin
Isoflavones are degraded by alkali as follows:

OH
~
° ~
I
~ OH- ~ + HCOOH
+ HCOOH
& &
~ ~
~
~ ~ Formic
Formic acid
acid
Isoflavone
Isoflavone Desoxybenzoin
Desoxybenzoin
AlkaljfUS~ ~hYlatjOn
O
OH
~
I +
e
~
I
OCH3
COOH
Isoflavones have shown estrogenic, insecticidal, and antifungal activity;
+
HOOCO
~
I
some of them are potent fish poisons.
4. Anthocyanins
The innumerable shades of blue, purple, and violet, and nearly all the reds
that appear in the cell sap of flowers, fruits, leaves, and stems of plants are
due to anthocyanin pigments in the dissolved state. The sugar-free pigments
are called anthocyanidins. The structure common to all anthocyanidins is the
flavylium (2-phenylbenzopyrylium) ion.
I. Flavonoids 7
The natural anthocyanidins may be classified into three groups: pelargonidin,

cyanidin, and delphinidin.
OH
OH
HO
Delphinidin
Various anthocyanins can be distinguished by partition between two immisci-

ble solvents, by their absorption spectra, and by their colors in buffer solu-
tions of graded pH. For structure determination, anthocyanidins are treated
with alkali, whereupon they form phloroglucinol and a phenolic acid:
Gallic acid
Delphinidin
Several factors, such as the pH, complex-forming metals, and tannins, affect
the colors of the anthocyanins.
5. Leucoanthocyanidins
Leucoanthocyanidins are flavan-3,4-diols. These colorless substances give red

solutions with acids. Leucoanthocyanidins are widely distributed in the plant
kingdom.
OH OH
HO
OH
HO HOHO
Melacacidin
Leucopelargonidin
OH
OH
HO.
Flavan-3,4-diols are sometimes obtained by reduction of flavonols of

flavanonols:
OH
HO HO
OH
HO HO
Dihydroquercetin Leucocyanidin
Biosynthetically, the flavonoid compounds are formed by the combina-

tion of a C 6 - C 3 fragment derived from shikimic acid, e.g., p-hydroxycinnamic
acid, with a six-carbon atom unit formed by the linear combination of three
acetate units:
<C~y~C-C-C + (C-CO)3
^^-C-C-C-C-CO-C-CO-C-COOH
I. Flavonoids 9
The following general scheme has been proposed for the biosynthesis of
compounds derived from shikimic acid: shikimic acid - > prephenic acid —»
p-hydroxyphenylpyruvic acid —> p-hydroxyphenyllactic acid —> p-hydroxy-
cinnamic acid —» flavones.
Hydroxylation of rings A and Β may occur at a stage after ring forma-
tion has been completed. Isoflavones are probably formed by phenyl migra-
tion of flavones.
B. Isolation of Hesperidin from Orange Peel
Hesperidin
1. Introduction
Hesperidin was first isolated by Leberton in 1828 from the albedo (the spongy
inner portion of the peel) of oranges of the family Hesperides, and was given
the name hesperidin (1). Its presence was detected in lemons by Pheffer as
early as 1874 (2). Neohesperidin, an isomer of hesperidin, has been isolated
together with hesperidin from unripe sour oranges cultivated in Europe (3).
Horowitz and Gentili (4) isolated it from Ponderosa lemon. Hesperidin was
isolated from Citrus mitis by Sastry and Row (5).
Neohesperidin, a bitter compound, occurs in the bitter orange, Citrus
aurantium, while hesperidin, a nonbitter compound, is the predominant
Flavonoid in lemons and the ordinary sweet orange, Citrus sinensis.
Hesperidin decreases the fragility of blood capillaries.
2. Principle
Hesperidin can be isolated by two methods: (a) by extracting the dry peel
successively with petroleum ether and methanol, the first solvent removing
the essential oil and the second, the glycoside; (b) by alkaline extraction of
chopped orange peel and acidification of the extract. It may be purified ef-
fectively by treatment with formamide-activated charcoal (6). Because of its
highly insoluble, crystalline nature, hesperidin is one of the easiest Flavonoids
to isolate.
3. Apparatus
Disintegrator
4. Materials
Acetic acid Formamide Methanol
Calcium hydroxide Hydrochloric acid Orange peel
Celite Isopropanol Petroleum ether
Ferric chloride Magnesium Sodium borohydride
5. Time
Method a, 4 - 5 hours; method b, soaking overnight, laboratory procedure 1-2
hours.
6. Procedure
a. Method a
Sun-dried peel 200 g is powdered in a disintegrator. The powder is placed in a
2-liter round-bottomed flask attached to a reflux condenser. One liter of
petroleum ether (bp 40-60°C) is added and heated on a water bath for
1 hour. The contents of the flask are filtered while hot through a Büchner
funnel, and the powder is allowed to dry at room temperature. The dry
powder is returned to the flask, and 1 liter of methanol is added. The contents
are heated under reflux for 3 hours and then filtered hot and washed with
200 ml hot methanol. The filtrate is concentrated under reduced pressure,
leaving a syrupy residue crystallized from dilute acetic acid, yielding white
needles; mp 252-254°C.
b. Purification of hesperidin with formamide

A 1 0 % solution of hesperidin in formamide, prepared by warming to about
60°C, is treated for 30 min with activated charcoal previously boiled with
dilute hydrochloric acid. The formamide, when tested in a 5 0 % aqueous
solution, should be slightly acid. If it is not acid, a little glacial acetic acid or
formic acid should be added. The solution is then filtered through Celite,
diluted with an equal volume of water, and allowed to stand for a few hours in
order to crystallize. The crystals of hesperidin are filtered off and washed, first
with hot water and then with isopropanol. Two such crystallizations give a
white crystalline product melting at 261 to 263°C.
c. Method b
Chopped orange peel 200 g and 750 ml 10% calcium hydroxide solution are
placed in a 2-liter Erlenmeyer flask and thoroughly mixed, then left overnight
at room temperature. The mixture is filtered through a large Büchner funnel
containing a thin layer of Celite on the filter paper. The yellow-orange filtrate
is acidified carefully to pH 4 - 5 with concentrated hydrochloric acid. Hesper-
idin separates as amorphous powder. It is collected on a Büchner funnel,
I. Flavonoids 11
washed with water, and recrystallized from aqueous formamide. If the pre-
cipitation of hesperidin on addition of hydrochloric acid is slow, it is advisable
to concentrate the solution under reduced pressure.
d. Ferric chloride test

Addition of ferric chloride solution to hesperidin produces a wine red color.
e. Magnesium-hydrochloric acid reduction test

Dropwise addition of concentrated hydrochloric acid to an ethanolic solution
of hesperidin containing magnesium develops a bright violet color.
f. Hesperidin
OMe
Rutinosyl-O
OH
OH 0
13
g. C-NMR (nuclear magnetic resonance spectrometry)
C-2 8 78.4 C-l' 131.2
C-3 42.0 C-2' 114.3
C-4 196.7 C-3' 146.7
C-5 163.0 C-4' 148.1
C-6 96.7 C-5' 112.7
C-7 165.2 C-6' 117.8
C-8 95.8 OMe 56.0
C-9 162.5
C-10 103.5
h. Mass spectrum
Hesperidin C 2 8 H 3 4 0 1 5, Molecular weight 610.
+
m/z 593(3%)[M + H - H 2 0 ] 303(100%) 413 ( 1 6 % )
465(34%) 449(28%)
References
1. Leberton, P. (1828). J. Pharm. Chim. Paris 14, 377.
2. Pheffer, W. (1874). Bot. Ztg. 32, 529.
3. Karrer, W. (1949). Helv. Chim. Acta. 32, 714.
4. Horowitz, R . M . , and Gentili, (1960). / . Am. Chem. Soc. 82, 2803.
5. Sastry, G . P., and Row, L . R . ( I 9 6 0 ) . / . Sei. Ind. Res. (India) 19B, 500.
6. Prichett, D . E . , and Merchant, H. E . (1946). J. Am. Chem. Soc. 68, 2108.
Recommended Reviews
1. Horowitz, R . M. (1961). The citrus flavonoids. In "The Orange" W. B . Sinclair, (ed.),
p. 334. University of California Press, Berkeley, Calif.
2. Seshadri, T. R . (1962). Isolation of flavonoid compounds from plant materials. In "The
Chemistry of Flavonoid Compounds" T. A. Geissman, (ed.), p. 6. Pergamon Press, London,
England.
C. Acidic Degradation of Hesperidin

1. Introduction
In 1929, Asahina and Inubuse (1) established the molecular formula of
hesperidin by showing that acid hydrolysis led to the formation of one mole
each of rhamnose, glucose, and the aglycone, hesperitin. Arthur, Hui, and
Ma (2) hydrolyzed hesperidin with 5 % sulfuric acid in ethylene glycol and
isolated the aglycone in an optically active form as the levorotatory isomer,
(-)-hesperitin. They therefore concluded that hesperidin is the 7-/3-
rutinoside of (-)-hesperitin. This was confirmed previously by the synthesis
of hesperidin by interaction of hesperitin and α-acetobromorutinose in the
presence of quinoline and silver oxide (3).
2. Principle
Hydrolysis of hesperidin with sulfuric acid in ethylene glycol under mild
conditions furnishes the aglycone, hesperitin, and one molecule each of
D-glucose and L-rhamnose (2). The carbohydrates are identified by circular
paper chromatography.
I. Flavonoids 13
3. Apparatus
Equipment for circular paper chromatography
4. Materials
Acetic acid n-Butanol Hesperidin
Ammonium hydroxide Ethanol Silver nitrate
Anisaldehyde Ethylene glycol Sulfuric acid
5. Time
2 - 3 hours
6. Procedure
One g hesperidin and 20 ml ethylene glycol containing 1 ml sulfuric acid are
heated on a steam bath for 40 min. The clear yellow solution is poured into
50 ml water. The precipitated hesperitin is filtered on a Büchner funnel
and washed with water. Crystallization from ethanol gives crystals of
mp 224-226°C yield, 350 mg. The filtrate, which contains sugars, is neu-
tralized and concentrated in vacuo until a thick syrup is obtained. The iden-
tification of the sugars is carried out by circular paper chromatography, the
developing solvent being n-butanol-acetic acid-water, 4 : 1 : 5 (v/v). The de-
veloped chromatogram is dried to remove the solvent and then sprayed with
one of the following reagents: (a) a mixture of equal volumes of aqueous
0.1NAgNO 3 and 57VNH 4OH; (b) a mixture of 0.5 ml anisaldehyde, 9 ml
ethanol ( 9 5 % ) , 0.5 ml concentrated sulfuric acid, and 0.1 ml acetic acid. The
chromatogram is then placed in an oven at 100 to 105°C for 5 to 10 min.
Color with Reagent
Sugar Rf a b
Glucose 0.29 brown blue

Rhamnose 0.48 brown green
a. UV spectrum of hesperitin
λ ™ 289 ταμ. (loge 4.27)
The Β ring of flavanones is not conjugated with the carbonyl group. Conse-
quently, their absorption is strongest in the 270-290 mμ region, associated
with that of the benzoyl grouping.
b. Hesperitin
OH
HO.
V
ζ /
OCR
13
b. C-NMR
C-2 78.5 C-l" 131.4
C-3 42.1 C-2' 114.3
C-4 196.2 C-3' 146.7
C-5 163.8 C-4' 148.1
C-6 96.2 C-5' 112.1
C-7 166.9 C-6' 118.0
C-8 95.4 CH30 55.9
C-9 163.0
C-10 102.1
d. Mass spectrum
Hesperitin C 1 6 H 1 4 0 6 , Mol. wt. 302.
m/z 331(9%) 303(100%) 179(6%) 153(4%)
304(18%) 287(6%) 177(1%)
References
1. Asahina, Y . , and Inubuse, M. (1929). / . Pharm. Soc. Japan 49, 128.
2. Arthur, H. R . , Hui, W. Η., and Ma, C. N. (1956). / . Chem. Soc. 632.
3. Zemplen, G . , and Bognar, R . (1943). Ber. 76B, 773.
Recommended Reviews
1. Horowitz, R . M. (1964). Relations between the taste and structure of some phenolic glyco-
sides. In "Biochemistry of Phenolic Compounds,'" J . B . Harborne, (ed.), p. 545. Academic
Press, New York.
2. Masami Shimokoriyama (1962). Flavanones, chalcones, and aurones. In "The Chemistry of
Flavanoid Compounds" T . Geissman, (ed.), p. 286. Pergamon Press, London, England.
3. Nagy, S., and Attaway, J . A . (eds.) (1980). "Citrus Nutrition and Quality." ACS Symposium
Series 143.
D. Isolation of Naringin from Grapefruit Peel

1. Introduction
The albedo, the spongy inner portion of the peel, is composed chiefly of
cellulose, soluble carbohydrates, pectic substances, flavonoids, amino acids,
I. Flavonoids 15
and vitamins. The flavonoid of the albedo is called naringin and was dis-
covered in 1866 by De Vry in the flowers of grapefruit trees of Java, see (1). It
was also isolated from the flowers and peel of Citrus decumana (2), from
grapes ( 3 ) , from the Japanese bitter orange ( 4 ) , from leaves of Pseudaegle
trifoliata ( 5 ) , and from other sources. One of the outstanding properties of
naringin is its intense bitterness; a hydrolytic enzyme (naringinase) is now
added to grapefruit juice in order to hydrolyze naringin to the nonbitter
naringenin (6).
C H 2O H
HO OH
Naringin
2. Principle
In the following procedure ( 7 , 8 ) naringin is extracted with hot water from the
grapefruit peel along with a small quantity of pectin. Concentration of the
extract to about one ninth the original volume affords naringin, as an octa-
hydrate. Recrystallization from isopropanol gives the pure dihydrate.
3. Apparatus
Blender
Vacuum distillation assembly
4. Materials
Celite Grapefruit peel
Ethanol Isopropanol
5. Time
4 - 5 hours
6. Procedure
One part chopped grapefruit peel and four parts water are heated to 90°C,
and maintained at this temperature for five min. The water extract is filtered
off. Two parts water are added to the solid; the extraction is repeated at 80°C
and immediately followed by filtration. The combined extracts are boiled with
1% Celite, filtered, and concentrated in vacuo to approximately one ninth
the original volume. The concentrated extract is allowed to crystallize in a
refrigerator and is then filtered as an octa-hydrate of mp 83°C (needles).
Naringin (8.6 g) is dissolved in 100 ml boiling isopropanol and filtered hot.
The filtrate is heated to its boiling point to initiate crystallization, then
allowed to cool, filtered on a Büchner funnel, and washed with cold isopropa-
nol; mp of dihydrate is 171°C (needles). Naringin can also be recrystallized
from a small amount of hot water.
a. Naringin
OH Ο
13
a. C-NMR
C-2 78.6 C-l' 128.7
C-3 42.0 C-2' 128.0
C-4 196.7 C-3' 115.3
C-5 162.9" C-4' 157.7
C-6 96.5 C-5' 115.3
C-7 164.9 C-6' 128.0
C-8 95.4
C-9 162.7"
C-10 103.5
c. Mass spectrum
Naringin 0 , 7 Η 3 20 1 4, Mol. Wt. 580.
+
m/z 581(100%)[M + H ] 579(100%)[M - H]
References
1. Will, W. (1885). Ber 18, 1311.
2. Zoller, H. F . (1918). Chem. Zentr. 89, 635.
3. Willimott, S. G. and Wokes, F . (1926). Biochem. J. 20, 1256.
4. Hattori, S., Shimokoriyama, M . , and Kanao, M. (1952). J. Am. Chem. Soc. 74, 3614.
5. Hattori, S., Hasegawa, M . , Wada, E . , and Matsuda, H. (1952). Kagaku {Science) 22, 312.
6. Ting, S. V . (1958). J. Agr. Food Chem. 6, 546.
7. Poore, H. D . (1934). Ind. Eng. Chem. 26, 637.
8. Hendrickson, R . , and Kesterson, J . W. (1956). Proc Florida State Horticultural Soc. 69, 149.
a
Values may be interchanged.
I. Flavonoids 17
Recommended Review
1. Horowitz, R . M. (1961). The citrus flavonoids. In: "The Orange." W. B . Sinclair, (ed.),
p. 334. University of California Press, Berkeley, Calif.
E. Synthesis of Naringin Dihydrochalcone—

A Sweetening Agent
1. Introduction
The peels of oranges, lemons, and grapefruits contain an array of Flavonoid
compounds of diverse type and structure. Two of the best known of these
compounds are hesperidin, the main flavonoid constituent of oranges and
lemons, and naringin, the main flavonoid constituent of grapefruit. These
substances have been known for more than a century and are characterized by
their abundance, accessibility, ease of isolation and intense bitterness (1).
OH
Naringin chalcone
Neo-O
H2
Pd/C
OH
Naringin dihydrochalcone
The relative bitterness of these flavonoids compared to quinine is shown

in the following table:
Relative
Compound Molarity Bitterness
4
Neohesperidin 5 x 10" 2
5
Naringin 5 x HT 20
6
Quinine 1 x 10" 100
Alkaline cleavage of ring C of naringin yields the corresponding chal-

cone, which is in turn hydrogenated catalytically to the corresponding in-
tensely sweet naringin dihydrochalcone (NDHC), which is about 1000 times
sweeter than sucrose.
The taste and the relative sweetness of dihydrochalcones and saccharin
are summarized in the following table.
Relative Sweetness
Compound Taste Molarity of Iso-Sweet Solution Molarity Weight

4
Naringin DHC Sweet 2 x 1(T 1 0.4
5
Neohesperidin DHC Sweet 1 x 10" 20 7
4
Saccharin (Na) Sweet 2 x 1(T 1 1
2. Principle
In the following procedure (2), an alkaline solution cleaves the heterocyclic C
ring of naringin, forming a chalcone that is subsequently hydrogenated to an
intensely sweet NDHC.
3. Apparatus
P A R R hydrogénation apparatus
4. Materials
Naringin Potassium hydroxide
Pd/C ( 1 0 % ) catalyst Sucrose
5. Time
4 hours
6. Procedure
A solution of 2 g naringin in 16 g 8.5% potassium hydroxide solution is placed
in a Parr pressure bottle and hydrogenated in a Parr shaker for 3 hr at an
initial pressure of 50 pounds per square inch gauge (psig) in the presence of
0.29 g 10% palladium on charcoal. The catalyst is filtered and the solution,
acidified to pH 6 with cold dilute hydrochloric acid. The precipitated NDHC
is filtered on a Büchner funnel and washed with cold water to yield 2.3 g of
the sweet product, mp 169-170°C.
The sweetness value of NDHC may be determined by panel evaluation
with a minimum of five people per panel. In a typical comparison test, a
I. Flavonoids 19
0.0045% solution of NDHC is compared with a 5 % solution of sucrose. The

product has a slight aftertaste.
References
1. Horowitz, R . M., and Gentiii, B . (1969). J. Agric. Food Chem. 17, 696.
2. Krbechek, L . , Inglett, G . , Holik, M., Dowling, B . , Wagner, R . , and Riter, R . (1968). / .
Agric. Food Chem. 16, 108.
Recommended Reviews
1. Crammer B . , and Ikan, R . (1977). Properties and synthesis of sweetening agents. Chem.
Soc. Revs. 6, 431.
2. Horowitz, R . M. (1964). Relation between the taste and structure of some phenolic glyco-
sides. In "Biochemistry of Phenolic Compounds(J. B . Harborne, ed.), p. 545. Academic
Press, New Y o r k .
3. Kinghorn, A . D . (1987). Biologically active compounds from plants with reputed medicinal
and sweetening properties. J. Nat. Products 50, 1009.
F. Color Changes of Anthocyanins at Various pH Values

1. Introduction
The term anthocyanin was proposed by Marquart in 1835 to denote the blue
pigment of the cornflower. Actually, the anthocyanins encompass the entire
range of red, violet, and blue pigments in plants. In general, the deepening of
the visible color is brought about by the increase in the number of hydroxyl
groups, as illustrated by the orange-red color of pelargonidin, the deep red of
cyanidin, and the bluish red of delphinidin derivatives. Color changes ranging
from violet to blue were first noted by Willstätter who observed that antho-
cyanins are red under acidic, violet under neutral, and blue under alkaline
conditions. The other factor that controls the coloration of flowers is the
coexistence of several anthocyanins, for instance malvidin and delphinidin in
the berries of Empetrum nigrum (1) and in the flowers of Althaea rosea (2). A
similar situation is encountered in a variety of garden plants (3).
Scott-Moncrieff (4) studied the interrelationship between color and the
acidity of the cell sap. Later, Shibata, Hayashi, and Isaka ( 5 ) , using petals,
fruits and leaves of 200 plants, showed that all the saps are invariably acidic,
irrespective of their color, the pH being around 5.5 in most cases. Robinson
and Robinson (6) held the view that tannins and flavone derivatives partici-
pate in anthocyanin co-pigmentation. Other investigators suggested that the
blue color is due to an insoluble organometallic complex containing magne-
sium or calcium, and that the violet color is produced by a mixture of blue
anthocyanins with red oxonium salts (7).
OH PH
ΗΟ^χ H O ^ Ο
OH O H
O H '
OG1 OG1
Cyanin cation Cyanin base
(pH < 3, red) (pH 8.5, violet)
H O ^
OGl
Cyanin anion
(pH > 11, blue)
2. Principle
The following experiment demonstrates the change in color of anthocyanin as
a function of pH. It is probable that the red color is due to the cationic form of
anthocyanin; the violet color is characteristic of the base, while blue is the
anionic form.
It is noteworthy that changes in color from red to mauve and purple,
which occur during flower development, have also been ascribed to pH
effects.
3. Apparatus
Burettes
Test tubes
4. Materials
Cabbage, red
Disodium phosphate ( N a 2 H P 0 4 )
Hydrochloric acid
Monopotassium phosphate ( K H 2 P 0 4 )
Pelargonium flowers
Roses
Sodium hydroxide
Tripotassium phosphate ( K 3 P 0 4 )
I. Flavonoids 21
5. Time
1-2 hours
6. Procedure
a. To 15 g well-washed red cabbage cut into small pieces is added 100 ml
water. The pigment is extracted by boiling for 15 min and is then filtered
into a measuring cylinder and made up to 50 ml with water. This solution is
then introduced into a burette from which 2-ml samples are added to each
of 18 test tubes containing the buffer solutions, and the resulting colors are
recorded.
b. A similar procedure is adopted for pelargonium and roses.
a
Preparation of the Solutions of the Phosphate B u f f e r
Test 0ΛΝ 0Λ5Μ 0.15M 0.15M

Tube HCl K H 2P 0 4 N a 2H P 0 4 K 3P O 4 pH
1 9.5 0.5 — — 2.1

2 0.5 9.5 — — 3.6
3 — 10.0 — — 4.7
4 — 9.5 0.5 — 5.6
5 — 9.0 1.0 — 5.9
6 — 8.0 2.0 — 6.2
7 — 7.0 3.0 — 6.5
8 — 6.0 4.0 — 6.6
9 — 5.0 5.0 — 6.8
10 — 4.0 6.0 — 7.0
11 — 3.0 7.0 — 7.2
12 — 2.0 8.0 — 7.4
13 — 1.0 9.0 — 7.7
14 — 4.5 — 5.5 8.0
15 — 5.0 — 5.0 9.8
16 — 3.0 — 7.0 10.7
17 — — 3.0 7.0 11.2
18 1 0 % NaOH — — — 14.0
"In ml.
References
1. Hayashi, K . , Suzushino, G . , and Ouchi, K. (1951). Proc. Japan Acad. 27, 430.
2. Karrer, P., and Widmer, R . (1927). Helv. Chim. Acta 10, 5.
3. Robinson, G. M . , and Robinson, R . (1932). Biochem. J. 26, 1647.
4. Scott-Moncrieff, R . (1939). Ergeb. Enzymforsch. 8, 277.
5. Shibata, K . , Hayashi, K . , and Isaka, T. (1949). Acta Phytochim. (Japan) 15, 17.
6. Robinson, G. M., and Robinson, R . (1931). Biochem. J. 25, 1687.

7. Bate-Smith, E . C., and Westall, R . G. (1950). Biochim. Biophys. Acta 4, 427.
Recommended Reviews
1. Goto, T . (1987). Structure, stability, and color variation in anthocyanins. Prog. Chem. Org.
Nat. Prod. 52, 113.
2. Harborne, J . B . (1968). Flavonoids: distribution and contribution to plant color. In "Chemis-
try and Biochemistry of Plant Pigments." (T. W. Goodwin, ed.), p. 247, Academic Press,
New York.
3. Kozo Hayashi. (1962) The anthocyanins. In "The Chemistry of Flavonoid Compounds"
(T. Geissman, ed.), p. 248, Pergamon Press, London, England.
G. Questions
1. Name the main groups of flavonoids.

2. What are polyphenolic compounds, and what is their function in
nature?
3. Which products are obtained by alkaline treatment of flavones and
anthocyanins?
4. Give examples of phenols that possess pharmacological and therapeutic
properties.
5. Outline the major pathways for the biosynthesis of flavonoids.
H. Recommended Books
I. Agrawal, P. K. (1989). "Carbon-13 NMR of Flavonoids:' Elsevier,

Amsterdam, the Netherlands.
2. Bentley, Κ. W. (1960). "The Natural Pigments:' Interscience, New
York.
3. Britton, G. (1983). "The Biochemistry of Plant Pigments" Cambridge
University Press, New York.
4. Dean, F. M. (1963). "Naturally Occurring Oxygen Ring Compounds:'
Butterworth, London, England.
5. Geissman, T. A. (ed.) (1962). "The Biochemistry of Plant Pigments."
Cambridge University Press, New York.
6. Harborne, J . B . (ed.) (1964). "Biochemistry of Phenolic Compounds"
Academic Press, New York.
7. Harborne, J . B . , Mabry, T. J . , and Mabry, H. (eds). "The Flavonoids,
Parts 1 and 2 . " (1975). Academic Press.
II. Lipids 23
II. LIPIDS
A. Introduction
Lipids can be classified into three groups: fats and oils, waxes, and phospholi-
pids. They occur in all parts of plant and animal tissue, and can be isolated by
extraction with organic solvents such as ether, acetone, alcohols, chloroform,
and petroleum ether.
1. Fats and Oils

The fat from a given source consists of a rather characteristic mixture of
glycerides. The glycerides are of two types, simple and mixed.
H 2 C O C O C 1 7H 3 5
I
H C O C O C 1 7H 3 5
I
H 2 C O C O C 1 7H 3 3
Oleodistearin (mixed glyceride)
The glycerides may be readily saponified into glycerol and salts of the
fatty acids.
The acids known to be present in various lipids vary in carbon content
from C 1 2 to C 3 4 and nearly always contain an even number of carbon atoms.
Many of these acids belong to the saturated aliphatic series, while others
contain from one to six double bonds. Recently, fatty acids containing triple
bonds and cyclic structures attached to the carbon chain have been dis-
covered. Pure acids can be isolated from the mixtures resulting from the
saponification of fats by the following procedures: fractional crystallization,
fractional distillation, preparation and debromination of polybromides, ad-
sorption chromatography, gas-liquid chromatography of methyl esters, and
preparation of urea fatty-acid complexes that are stable to oxidation and
are a convenient form for storing polyunsaturated acids. Urea binds fatty
acids in a ratio of approximately 3:1 by weight. Desoxycholic acid is one
of the compounds forming inclusion compounds with fatty acids; it forms
choleic acids.
Most of the unsaturated acids, including the most important non-
conjugated acids (oleic, linoleic and linolenic), occur naturally as the
eis form.
A Number of the Natural Fatty Acids
Saturated acids
Caproic C 5H nC O O H Palmitic C 1 5H 3 1C O O H
Caprylic C 7 H 1 5C O O H Stearic C 1 7H 3 5C O O H
Capric C 9 H 1 9C O O H Arachidic C 1 9H 3 9C O O H
Laurie C n H 2 3C O O H Behenic C 2 1H 4 3C O O H
Myristic C n H 2 7C O O H Montanic C 2 7H , 5 C O O H
Unsaturated acids
Oleic C 1 7H 3 3C O O H C H 3( C H 2) 7C H = C H ( C H 2) 7C O O H
Linoleic C 1 7H 3 1C O O H C H 3( C H 2) 4C H = C H C H 2C H = C H ( C H 2) 7C O O H
Linolenic C 1 7H 2 9C O O H C H 3C H 2C H = C H C H 2C H = C H C H 2C H = C H ( C H 2) 7C O O H
Arachidonic C 1 9H 3 1C O O H C H 3( C H 2) 4( C H = C H C H 2) 4( C H 2) 2C O O H
Clupanodonic C H 3( C H 2C H = C H C H 2) 2C H = C H C H 2
( C H 2C H = C H C H 2) 2— C H 2C O O H
Nisinic C 2 3H 3 5C O O H C H 3C H 2( C H = C H C H 2) 4( C H 2C H = C H C H 2) 2C H 2C O O H
Acetylenic acids
Tariric C 1 7H 3 1C O O H C H 3 ( C H 2 ) K )= C ( C H 2 ) 4 C O O H
Stearolic C 1 7H 3 1C O O H C H 3( C H 2) 7C = C ( C H 2) 7C O O H
Ximenynic C 1 7H 2 9C O O H C H 3( C H 2) 5C H = C H — C = C ( C H 2) 7C O O H
Hydroxy acid
Ricinoleic C 1 7H 3 2( O H ) C O O H C H 3( C H 2) 5C H ( O H ) C H 2C H = C H ( C H 2) 7C O O H
Cyclic acids / V
Sterulic C 1 8H 3 3C O O H C H 3( C H 2) 7C = C ( C H 2) 7C O O H
Chaulmoogric C 1 7H 3 1C O O H ( C H 2 ) 1 2C O O H
Gorlic C 1 7H 2 9C O O H ( C H 2) 6C H = C H ( C H 2) 4C O O H
Although most naturally occurring fatty acids are straight-chain

compounds, there are certain exceptions, such as isovaleric acid,
( C H 3 ) 2 C H C H 2 C O O H . The main reactions of unsaturated acids involve the
addition of hydrogen, or halogen and oxidation.
C H 3( C H 2) 7C H = C H ( C H 2) 7C O O H C H 3( C H 2) 7C H 2C H 2( C H 2) 7C O O H
Oleic acid j Stearic acid
C H 3( C H 2) 7C H — C H — ( C H 2) 7C O O H
Br Br
9,10-Dibromostearic acid
II. Lipids 25
Chlorine and iodine, or iodine chloride may be added in a similar

manner.
Careful oxidation of oleic acid with alkaline permanganate at low
temperatures gives rise to the formation of dihydroxystearic acid; at higher
temperatures, the molecule is broken up into two acids of nine carbon atoms
each.
C H 3( C H 2) 7C H = C H ( C H 2) 7C O O H C H 3( C H 2) 7C H — C H ( C H 2) 7C O O H
ι οc
Oleic acid
KMn04 OH OH
Dihydroxystearic acid
C H 3( C H 2) 7C O O H + H O O C ( C H 2) 7C O O H
Pelargonie acid Azelaic acid
Ozone adds to the double bonds of unsaturated acids, forming an

ozonide, which is split into two aldehydes.
H H
I I
C H 3 ( C H 2 ) 7 C H = C H ( C H 2 ) 7 C O O H — U C H 3( C H 2) 7— € — O — C — ( C H 2) 7C O O H
\>—Ο
ι
C H 3( C H 2) 7C H O + O H C ( C H 2) 7C O O H
Pelargonie aldehyde Azelaic semialdehyde
2. Waxes
The waxes consist essentially of esters of fatty acids and monohydric alcohols
that contain from 24 to 36 carbon atoms. The following are examples of
important natural waxes: beeswax, which contains, among other constituents,
palmitic ( C 1 6 ) and cerotic ( C 2 6 ) acids and melissyl alcohol ( C 3 0) ; lanolin—a
waxy material obtained from wool; spermaceti—found in the head of the
sperm whale and containing cetyl and oleyl alcohols and palmitic acid. The
waxes are more resistant to saponification than are fats and oils.
3. Phospholipids
Phospholipids are fat-like substances containing (in addition to fatty acids
such as oleic or stearic acid) phosphoric acid; a nitrogenous base such as
choline, found in lecithin; or ethanolamine or serine, present in cephalins;
and a polyhydroxy alcohol, either glycerol or inositol.
Β. Isolation of Trimyristin and Myristicin from Nutmeg

1. Introduction
Nutmeg oil is obtained by steam distillation of the kernels of the fruit of
Myristica fragrans Houttayn, a tree 15-20 meters high, grown in Indonesia
and in the West Indies. Nutmeg oil consists of approximately 9 0 % of terpene
hydrocarbons. Major components are sabinene, and a- and β-pinene. A
major oxygen-containing constitutent is terpinen-4-ol. A fraction consisting
of phenols and aromatic ethers, such as safrole, myristicin, and elemicin, is
responsible for the characteristic nutmeg odor.
OCH3
Ο
H 2C H 2C
Ο C H 2C H = C H 2 & ^ C H 2C H = C H 2
safrole myristicin
OCH3
C H 2C H = C H 2
elemicin
Nutmeg oil is used mainly in food flavoring, and to a lesser extent in

perfumery.
Semmler (1) isolated myristicin from the seeds of Myristica fragrans
(nutmeg) in 1890. It was also found in French parsley ( 2 ) , in the ethereal oil
of the plant Cinnamomum glanuliferum (3), in the orthodon oil (4), and in
Ridolfia segetum (up to 3 3 % ) (5).
Many investigators have succeeded in isolating the ester trimyristin from
nutmeg by ether extraction ( 6 , 7 ) . Although myristicin is not a lipid, it is a
byproduct of the extraction of nutmeg. Myristicin is toxic and has narcotic
activity.
C H 2 O C O C 1 3H 2 7 C H 2O H
I Κ OH I
C H O C O C 13 3 H 277 2 -ÎL+
1 CHOH + 3 C 1 3H 2 7C O O H
I C 2H 5O H I
I I Myristic acid
C H 2 O C O C 1 3H 2 7 C H 2O H
Trimyristin Glycerol
II. Lipids 27
2. Principle
Isolation of trimyristin (ester) and myristicin (phenylpropane derivative), the
two major products of nutmeg, is accomplished by extraction with chlo-
roform. These compounds are separated by removing the solvent and then
filtering.
The solid trimyristin is treated with alkali, yielding myristic acid. Myris-
ticin is purified by column chromatography and fractional distillation. Upon
bromination, it forms a solid dibromo derivative.
3. Apparatus
Reflux assembly
4. Materials
Alumina Ether Petroleum ether
Bromine Hydrochloric acid Potassium hyddroxide
Ethanol Nutmeg
5. Time
Isolation of trimyristin: 3 hours
Isolation of myristicin: 1-2 hours
6. Procedure
a. Isolation of trimyristin
Thirty g crushed nutmeg and 200 ml chloroform are refluxed for 90 min on a
water bath, filtered through a folded filter paper, and dried on calcium
chloride. The chloroform solution is then filtered, and the solvent is distilled
under reduced pressure, leaving a semisolid residue, which is dissolved in
200 ml ethanol ( 9 5 % ) . On cooling, crystalline trimyristin precipitates and is
filtered off with suction and washed with cold ethanol ( 9 5 % ) . The crystals are
colorless and odorless and melt at 54 to 55°C yield, 6 g. The filtrate and
washings are kept for the isolation of myristicin.
b. Trimyristin
C H 2 O C O C 1 3H 2 7
C H O C O C 1 3H 27
C H 2 O C O C 1 3H 2 7
c. Mass spectrum
Trimyristin C 4 5 H 8 6 0 6 , Mol. wt. 722.
m/z 724(21%) 722(26%) 105(20%) 41(100%)
723(55 % ) 495(43 % ) 57(46% )
d. Infrared spectrum (IR) (in CS 2)

1
2700 c m " : C—H stretching vibrations
1748: C = 0 stretching of saturated ester
1363: sym. deformation vibrations of C H 3 group
1231, 1154, 1106: asym. stretching of ester C—Ο—C (common to all
triglycerides of long-chain fatty acids)
1035: sym. stretching of ester C—Ο—C
710: C H 2 wagging
e. Saponification of trimyristin
Five g trimyristin and 75 ml 3.5% ethanolic potassium hydroxide are refluxed
for 1 hr on water bath, 150 ml water is added, and ethanol is removed under
reduced pressure. After filtration, the solution is acidified with hydrochloric
acid and left at room temperature until the myristic acid solidifies. The acid is
filtered on a Büchner funnel and washed with water. Recrystallization from
dilute ethanol gives a yield of 2 g acid, mp 51-52°C.
f. Thin-layer chromatography of nutmeg constituents

The crude extract is spotted on a thin layer plate (Silica Gel G F 2 5 )4 and
developed with dichloromethane. The dry plate is then sprayed with anisal-
dehyde-sulfuric acid reagent, (as described in the T L C of black pepper
extract). Myristicin appears as a violet-red spot, Rf0.72.
g. Isolation of myristicin
On concentration of the mother liquor remaining after separation of trimyris-
tin, a residue is obtained, which is dissolved in 20 ml petroleum ether and
passed through a short column containing 10 g activated alumina. Elution
with 150 ml petroleum ether and evaporation of the solvent leaves an oil,
which is fractionally distilled. Bp 150°C/15 mm, yield, 2.5 g.
Myristicin
C H 2— C H = C H 2
II. Lipids 29
Mass spectrum
Myristicin C u H 1 2 0 3 , Mol wt. 192.
m/z 192(100%) 161(14%) 119(15%) 65(16%)
165(23%) 131(13%) 91(25%) 39(13%)
h. Preparation of dibromo myristicin

Bromine (0.4 ml) is added dropwise to 5 ml cold ether (ice bath). The
resulting solution is then added slowly to 1 g myristicin in 25 ml petroleum
ether until no further change in the color of bromine is observed. The
dibromo derivative separates as fine needles, which are filtered and washed
with petroleum ether, mp 124°C.
i. IR spectrum of myristic acid (in CS 2)

- 1
3500-3000 c m : the OH of the C O O H group is strongly bonded and
responsible for the broad absorption band that commences at about
1
3500 c m " and extends into the region of the C—H stretching
- 1
absorption below 3000 c m
2650: C—H stretching vibrations
1760: a weak band due to the carbonyl group of the monomer
1708: a strong carbonyl band associated with the dimeric carboxylic
acid group
1290: coupling between in-plane Ο—Η bending and C—Ο stretching
of dimer
940: Ο—Η out-of-plane bending of dimer
720: C H 2 rocking
References
1. Semmler, F . W. (1890). Ber. 23, 1803.
2. Thomas, H. (1903). Ber. 36, 3451.
3. Pickles, S. S. (1912). J. Chem. Soc. 101, 1433.
4. Huzita, I. (1940). J. Chem. Soc. Japan 61, 729.
5. Gattefosse, J . , and Igolen, G. (1946). Bull. Soc. Chim. France 361.
6. Power, F . B . , and Salway, A . H. (1908). / . Chem. Soc. 93, 1653.
7. Verkade, P. E . , and Coops, J . (1927). Ree. Trav. Chim. 46, 528.
Recommended Reviews
1. de Stevens, G . , and Nord, F. F . (1955). Natural phenylpropane derivatives. In "Modern

Methods of Plant Analysis(K. Paech, and M. V . Tracey, eds.), Vol. 3, p. 428. Springer-
Verlag, New York.
2. Guenther, E . (1952). Oils ofMyristica. In "The Essential Oils" Vol. 5, p. 59. Van Nostrand,
New York.
C. Preparation of Azelaic Acid from Castor Oil

1. Introduction
Azelaic acid can be prepared by oxidation of castor oil with nitric acid ( 1 , 2 ) ,
by oxidation of ricinoleic acid with nitric acid (3) and alkaline permanganate
(4), by oxidation of methyl oleate with alkaline permanganate ( 5 ) , by the
ozonization of oleic acid and decomposition of the ozonide ( 6 ) , by trie
ozonization of methyl ricinoleate and decomposition of the ozonide (7), by
the Grignard reaction with 1,7-heptamethylenemagnesium dibromide (8), by
the oxidation of dihydroxystearic acid with dichromate in sulfuric acid ( 9 ) ,
and by other methods.
KOH
Castor oil C H 3( C H 2) 5C H ( O H ) C H 2C H = C H ( C H 2) 7C O O H
C H OH
2 5 Ricinoleic acid
KMnO,
HOOC—<CH 2 ) 7 —COOH
Azelaic acid
2. Principle
Castor oil is the glyceryl ester of ricinoleic acid. It is abundant in nature and
has many industrial applications.
In the following experiment (10), castor oil is hydrolyzed with alkali,
yielding crude ricinoleic acid, which is oxidized with potassium permanganate
to give azelaic acid.
3. Apparatus
Stirrer
4. Materials
Castor oil Magnesium sulfate Potassium permanganate
Ethanol Potassium hydroxide Sulfuric acid
5. Time
4 - 5 hours
6. Procedure
Fifty g castor oil is added to a solution of 50 g potassium hydroxide in 100 ml
9 5 % ethanol. The mixture is placed in a 500-ml flask equipped with a reflux
II. Lipids 31
condenser and is boiled for 3 hr. The solution is then poured into 300 ml
water and acidified by addition of a solution of 10 ml concentrated sulfuric
acid in 30 ml water. The acid that separates is washed twice with warm water.
The yield of crude oily ricinoleic acid thus obtained is 48 g.
The 48 g ricinoleic acid is dissolved in 320 ml water containing 13 g
potassium hydroxide. In a 2-liter round-bottomed flask equipped with a
powerful mechanical stirrer are placed 135 g potassium permanganate and
1.51 water at 35°C. The mixture is stirred to facilitate solution of the perman-
ganate, and, if necessary, heat is applied to maintain the temperature at 35°C.
When the permanganate has completely dissolved, the alkaline solution of
ricinoleic acid is added in a single portion with vigorous stirring. The tempera-
ture rises to about 75°C. Stirring is continued for half an hour, or until a test
portion added to water shows no permanganate color. To the mixture is now
added a solution of 80 g concentrated sulfuric acid in 250 ml water. The acid
must be added slowly and carefully to prevent too rapid evolution of carbon
dioxide with consequent foaming. The mixture is heated on a steam bath for
15 min to coagulate the manganese dioxide, which is filtered while still very
hot. After filtration, the manganese dioxide is placed in a 400-ml beaker and
boiled with 200 ml water in order to dissolve any azelaic acid that may adhere
to it. This mixture is filtered while hot, and the filtrate is added to the main
portion. The combined filtrates are evaporated to a volume of about 800 ml,
and this solution is cooled in ice. The crystals that separate are filtered with
suction, washed once with cold water, and dried. The yield is 14-16 g mate-
rial of mp 95-106°C. The crude substance is dissolved in 240 ml boiling water,
filtered with suction, and allowed to cool. The crystals are filtered, washed
with water, and dried; yield, 10-11 g; mp 104-6°C.
a. Azelaic acid
Ç H 2— C H 2— C O O H
( Ç H 2) 3
C H 2— C H 2— C O O H
b e d
1
b. H NMR
a = 1.27 6H c = 2.20 4H
b = 1.48 4H d = 11.93 2H
c. Mass spectrum
Azelaic acid C 9 H 1 6 0 4 , Mol. wt. 188.
m/z 84(39%) 69(51%) 55(100%) 43(42%)
83(41%) 60(61%) 45(46%) 41(80%)
References
1. Day, J . N. E . , Kon, G. A. R . , and Stevenson, A . (1920). J. Chem. Soc. 117, 642.
2. Boeseken, J . and Lutgerhorst, A. G. (1932). Ree. Trav. Chim. 5 1 , 164.
3. Verkade, P. E . (1927). Ree. Trav. Chim. 46, 137.
4. Maquenne, M. L. (1899). Bull. Soc. Chim. 21 ( 3 ) , 1061.
5. Armstrong, E . F . , and Hilditch, T. P. (1925). J. Soc. Chem. Ind. 44, 43T.
6. Harries, C., and Tank, L. (1907). Ber. 40, 4556.
7. Haller, Α . , and Brochet, A . (1910). Compt. Rend. 150, 500.
8. von Braun, J . , and Sobecki, W. (1911). Ber. 44, 1926.
9. Bennet, G. M., and Gudgeon, H. (1938). / . Chem. Soc. 1679.
10. Hill, J . W., and McEwen, W. L. (1950). Org. Synth. Coll. 2, 53.
D. Formation of n-Heptaldehyde and Undecenoic Acid

from Castor Oil
1. Introduction
Castor oil is a readily available substance. It may undergo scission into
10-undecenoic acid and heptaldehyde, or it may be dehydrated to form
9,11-octadecadienoic and 9,12-octadecadienoic (linoleic) acids. The dehy-
dration reaction is facilitated by the presence of dehydrating catalysts such as
aluminum oxide, phosphoric anhydride, and similar substances, while the
scission reaction appears to be characteristic of thermal degradation.
The pyrolysis of castor oil was first carried out by Bussy and Lecanu
(1) in 1827. Some years later, Bussy identified heptaldehyde in the liquid
product (2). In 1877, Krafft (3) identified the second compound as 10-
undecenoic acid.
Perkins and Cruz (4), and more recently, Vernon and Ross (5), have
verified the formation of 10-undecenoic acid; in the first case by distillation at
400°C (50 mm) and in the second by pyrolysis in a silica tube. Barbot (6) has
proposed a mechanism for his cleavage.
Castor oil C H 3( C H 2) 5C H O + C H 2= C H ( C H 2) 8C O O H
Heptaldehyde 10-Undecenoic acid
2. Principle
Pyrolysis of castor oil (which consists of about 8 0 % triricinolein) under
reduced pressure produces a mixture of heptanal and 10-undecenoic acid (7).
These componds are then separated by fractional distillation. «-Hept-
aldehyde is identified as the 2,4-dinitrophenylhydrazone.
II. Lipids 33
3. Apparatus
Fractionation column
4. Materials
Castor oil Colophony 2,4-Dinitrophenylhydrazine
5. Time
2 - 3 hours
6. Procedure
Castor oil (150 g) and 10 g colophony are mixed in a Claisen flask fitted for
vacuum distillation and heated over a bare flame. After 10 to 15 min, the
distillate begins to collect in the receiving flask. When approximately 60 to
80 ml has been collected, the heating is stopped (to avoid the formation of
the yellow resinous paste in the flask, which is very difficult to remove).
If two layers are formed in the distillate, the lower one (water) is
removed by means of a separatory funnel, and the upper one is poured into a
500-ml flask to which is attached an efficient fractionation column; the distil-
late passing between 145°C and 160°C is collected (crude heptaldehyde), and
when the temperature rises above 170°C, the distillation is interrupted. The
crude heptaldehyde is purified by a second distillation. The yield is about
24 to 30 g. The 2,4-dinitrophenylhydrazone crystallized from ethanol forms
orange needles, mp 108°C.
The residue of the fractional distillation is distilled in vacuo. The un-
decenoic acid distils between 156 and 165°C at 30 mm, giving a yield of
25 to 30 g.
a. IR (liquid film)
- 1
3065 c m : dimeric Ο—Η stretching
2915, 2850, 2650: characteristic of a dimeric carboxylic acid
1710: C = 0 stretching, characteristic of a dimeric acid
1645: C = C stretching, characteristic of the monosubstituted double
bond
1415, 1285, 1245: coupling between in-plane Ο—Η bending and C—Ο
stretching of dimeric acid
990, 910: C—Η out-of-plane bending of terminal methylene
720: methylene chain rocking
b. 10-Undecenoic acid
He
C = C — C H 2— ( C H 2) 5- C H 2- C H 2- C O O H
Hf Hg
1
b. H NMR
a = 1.30 (10H) e = 4.93 (1H)
b = 1 . 6 2 (2H) f = 4.98 (1H)
c = 2.03 (2H) g = 5.80 (1H)
d = 2.35 (2H) h = 10.80 (1H)
d. Mass spectrum
10-Undecenoic acid C n H 2 o 0 2 , Mol. wt. 184.
m/z 96(30%) 82(30%) 69(44%) 55(100%)
83(38%) 73(29%) 60(27%) 41(56%)
References
1. Bussy, J . , and Lecanu. (1827). / . Pharm. Chim. 13 ( 2 ) , 57.
2. Bussy, J . (1845). / . Pharm. Chim. 8 ( 3 ) , 321.
3. Krafft, F . (1877). Ber. 10, 2034.
4. Perkins, G. Α . , and Cruz, A . O. (1927). J . Am. Chem. Soc. 49, 1070.
5. Vernon, Α . Α . , and Ross, Η. K. (1936). J . Chem. Soc. 58, 2430.
6. Barbot, A . (1935). Bull. Soc. Chim. 2 ( 5 ) , 895.
7. Dominguez, Χ . Α . , Speron, E . , and Slim, J . (1952). / . Chem. Educ. 29, 446.
Recommended Review
1. Sonntag, Ν. Ο. V . (1961). Dehydration, pyrolysis, and polymerization. In "Fatty Acids"
(K. S., Markley, ed.), Vol. 2, p. 985. Interscience, New York.
E. Ozonization of Methyl Oleate
1. Introduction
The ozonide of oleic acid and the cleavage products obtained by treatment
with water (azelaic semialdehyde, azelaic acid, pelargonaldehyde, and pelar-
gonic acid) were first described by Harries and Thieme (1), who used no
solvent for the ozonization. Subsequently, hexane (2), chloroform (3), glacial
acetic acid (4), ethyl chloride (5), and ethyl acetate (6) were used as solvents.
The highest yields were obtained by ozonization in glacial acetic acid, fol-
lowed by reduction with zinc (4). Azelaic semi-aldehyde has been isolated,
with 8 0 % yield, as the semicarbazone by ozonization in ethyl chloride,
II. Lipids 35
followed by catalytic hydrogénation in methanol (5). Recent studies of the

ozonization of various unsaturated compounds have shown methanol and
ethanol to be superior reaction media, providing increased yields of the
isolated carbonyl compounds.
Privett and Nickell (7) recently found that ozonization of methyl
oleate produced nine compounds, which were identified by thin-layer
chromatography.
C H 3( C H 2) 7C H = C H ( C H 2) 7C O O C H 3
Methyl oleate
1. 0 3 J 2. Zn/AcOH
C H 3( C H 2) 7C H O + C H 3O O C ( C H 2) 7C H O
Pelargonaldehyde Methyl semiazelaaldehyde
2. Principle
In the following experiment ( 8 ) , methyl oleate is ozonized in methanol. The
ozonide formed is cleaved with zinc dust in acetic acid.
The resulting pelargonaldehyde and methyl semiazelaaldehyde are
separated by fractional distillation.
3. Apparatus
Ozonator
4. Materials
Acetic acid Methylene chloride
Calcium sulfate, anhydrous Ozone
Methanol Potassium iodide
Methyl oleate Zinc dust
5. Time
2 - 3 hours
6. Procedure
Methyl oleate (24 g) is dissolved in 360 ml reagent-grade methanol in a 1-liter
round-bottomed flask equipped with an inlet tube, and cooled to - 2 0 ° C . Dry
ozone is passed through the solution until the potassium iodide solution at the
outlet of the reactor becomes strongly colored, indicating that ozone is no
longer being absorbed. Glacial acetic acid (30 ml) is added, and the solution is
warmed to 30°C. Zinc dust is added, a small pinch at a time, until a total of
12 g has been introduced, the temperature being maintained at 30 to 35°C by

cooling. The mixture is then filtered and distilled on a steam bath until about
one half of the methanol has been removed. Methylene chloride (100 ml)
and 100 ml water are added, and the layers separated. The methylene chlor-
ide layer is washed with water until free of acid. It is then dried over anhy-
drous calcium sulfate. It should be noted that the washing should be carried
out as soon and as thoroughly as possible; otherwise, varying amounts of
the dimethyl acetal will form. Methylene chloride is removed from the
solution by distillation on a steam bath. The residue is distilled in vacuo
through a small Vigreux column, and two main fractions are obtained: 8.5 g
pelargonaldehyde boiling at 37 to 47°C/0.3 mm, n^ = 1.4193; and 12 g
methyl semiazelaaldehyde, bp 94-96°C/0.75 mm,rcff= 1.4348.
References
1. Harries, C , and Thieme, C. (1905). Ann. 343, 318.
2. Molinari, E . , and Soncini, E . (1906). Ber. 39, 2735.
3. Harries, C. (1906). Ber. 39, 3728.
4. Noller, C. R . , and Adams, R . (1926). J. Am. Chem. Soc. 48, 1074.
5. Fischer, F . G . , Dull, H., and Ertel, L. (1932). Ber. 65B, 1647.
6. Stoll, M., and Rouve, A . (1944). Helv. Chim. Acta 27, 950.
7. Privett, O. S., and Nickeil, E . C. (1964). J. Am. Oil Chemists' Soc. 41, 72.
8. Pryde, Ε . H., Anders, D . E . , Teeter, H. M , and Cowan, J. C. (1960). J. Org. Chem. 25,
618.
Recommended Review
1. Kadesch, R . G. (1963). Ozonolysis of fatty acids and their derivatives. In "Progress in the
Chemistry of Fats and Other Lipids," ( R . T . Holman, W. O. Lundberg, and T. Malkin,
eds.), Vol.6, p. 291. Pergamon Press, London, England.
F. Preparation of Urea Inclusion Compounds

(m) Urea 4- (n) Guest molecule ^ Inclusion compound
1. Introduction
The chemistry of (inclusion) clathrate (from the Latin word clathratus, which
means enclosed behind bars) compounds has a long history, starting at the
beginning of the nineteenth century. The most important event, however,
emerged from the pioneering X-ray structural work of H. M. Powell on S 0 2
clathrate of hydroquinone. It was found that the size, the shape, and the
chemical nature of the holes generated in an inclusion (host) lattice are the
key factors in allowing the selective inclusion of the guest molecules. Chemi-
cally different species as well as constitutional isomers, positional isomers,
regioisomers, stereoisomers, and even isotopic isomers are separated by this
technique. In general, lattice inclusion will cause altered physical properties
II. Lipids 37
of the guest molecules, and toxicity may be reduced. Studying the nature of
inclusion compounds requires special spectroscopic techniques for the solid
state, such as Raman, magic-angle spinning spectroscopy,high-resolution
electron microscopy, and X-ray crystallography.
The terms canal, channel, tube, and tunnel have been used to describe
host cavities extended in one dimension without restriction on cross-sectional
shape. Among the helical canal inclusion network (Fig. 1) are urea, thiourea,
deoxycholic acid, tri-o-thymotide, amylase compounds, and others.
In 1940, Bengen discovered that urea formed crystalline addition com-
pounds with a great variety of aliphatic, straight-chain molecules containing
more than six carbon atoms. In the presence of straight-chain hydrocarbons,
(A) X
H 2N NH2
(B)
HO*
(C)
Figure 1.1 Among the helical canal inclusion network are (A) urea, when
χ = 0, and thiourea, when χ = S; (Β) deoxycholic acid; and (C) tri-o-thymotide.
Figure 1.2 Structure of hexagonal urea. Solid circles represent urea

molecules.
urea forms a hexagonal lattice with internal channels (Fig. 2 ) . In these chan-
nels, the paraffin molecules are surrounded by urea and are thus kept firmly
in position. The diameter of these channels is ca. 5 Â, thus permitting the
entrance of only unbranched paraffins ( 1 , 2 ) in an extended planar zigzag
conformation. Branched molecules are generally excluded, unless branching
occurs near the end of a long linear chain. The complexes of thiourea have a
very similar structure (3), the sole difference being that in the thiourea lattice,
the diameter of the channel is ca. 7 Â. Consequently, thiourea forms inclu-
sion compounds only with larger molecules, since smaller molecules would
leave too much of the channel cavity unfilled, and the structure would
collapse.
Urea complexes meet almost all the requirements of an ideal derivative.
For example, they form large, easily handled crystals; no special reagents or
techniques are required for their preparation; the organic compound bound
in the complex is readily recovered by addition of water to dissolve the urea;
and the weight ratio of urea to organic compound is 3 : 1 , thus allowing for a
significant increase in the weight of material to be handled. In determining
the melting point of urea complexes by the capillary method, it is observed
that there is an exudation of a small amount of liquid before the melting point
is reached. The temperature at which opacity occurs, the complex dissociates,
and the transparent hexagonal crystals are converted to an aggregate of
tetragonal microcrystals without losing their original external form is termed
the dissociation temperature of a urea complex.
II. Lipids 39
The preparation of urea complexes of long-chain fatty acids, esters,

and alcohols has been reported by many investigators ( 4 - 6 ) . It was found
that several factors influence the yields of complexes of fatty acids. In the
saturated series, the longer the chain, the higher the yield. Among the
unsaturated, nonconjugated acids, increasing unsaturation lowers the yield.
Conjugated isomers give higher yields of complex than do nonconjugated
isomers. Trans monounsaturated acids give slightly higher yields than their eis
isomers. These differences in yields of complexes from the various fatty acids
suggest that the various types of acids can be fractionated by means of urea
complexes. The structure of urea complexes with unsaturated acids would
appear to indicate that they are excellent protectors against oxidation.
Urea inclusion compounds have been extensively applied in petrol
purification, dewaxing of lubricating oil, purification of terpenes, and the
separation of optical isomers.
2. Principle
Table 6 in the following description of preparations of urea complexes shows
that the dissociation temperature increases uniformly with increasing chain
length. Thus, the difference between the dissociation temperatures of the
urea complexes of lauric and stearic acids is about 33°C, while the melting
points of the commonly used derivatives of C 1 2 to C 1 8 fatty acids are usually
close together. Therefore, this feature is of great utility for identification
purposes. Another point of interest is the comparison of the dissociation
temperatures of the C 1 8 cis-trans isomers. The dissociation temperature of
the trans isomer is significantly higher than that of the eis isomer. Since the
eis compounds have some steric strain and are therefore less stable than the
trans ones, they dissociate at lower temperatures. Furthermore, binary mix-
tures of saturated and unsaturated fatty acids and of natural oils can be
separated on the basis of the difference in the rates of formation of the inclu-
sion complexes (5).
3. Apparatus
Microscope
4. Materials
Capric acid Linoleic acid Palmitic acid
Caproic acid Linolenic acid Pelargonie acid
Caprylic acid Linseed oil Petroleum ether
Corn oil Methanol Soybean oil
Elaidic acid Myristic acid Stearic acid
Hydrochloric acid Oleic acid Tridecyclic acid
Isopropanol Olive oil Urea
Lauric acid
5. Time
1-2 hours
6. Procedure
a. Urea complexes of fatty acids
The complexes of the series of pure fatty acids are prepared in the following
manner: 1 g fatty acid is dissolved by warming in 30 ml methanol that has
been saturated with urea at room temperature (about 1 6 g / 1 0 0 m l ) . If the
acid does not dissolve completely, a small quantity of isopropanol is added.
Upon cooling to room temperature, the mixture deposits crystalline urea
complexes, which are filtered off and dried. The products are crystallized
from methanol or isopropanol, and examined under a microscope or a mag-
nifying glass.
The dissociation temperatures of fatty acids and the molar and weight
ratios of urea to fatty acid are summarized in the following table.
Ratio of Urea to Acid
Acid °C Molar Weight
Caproic 64 — —
Caprylic 73 6.7 2.8
Pelargonie 80.5 7.4 2.8
Capric 85 8.0 2.8
Lauric 92.5 9.7 2.9
Tridecylic 96 11.8 3.3
Myristic 103 10.6 2.8
Palmitic 114 12.0 2.8
Stearic 126 14.7 3.1
Oleic (eis) 110 13.6 2.9
Elaidic (trans) 116 13.6 2.9
b. Separation of binary mixtures of fatty acids

The following table shows series of saturated and unsaturated fatty acids that
can be separated on the basis of the difference in the rates of formation of
their urea inclusion complexes.
Acids Urea (g) Methanol (ml) Complex Fraction Soluble Fraction
9.9 g lauric 30 150 10.5 g 8.3 g

9.9 g stearic 8 8 % stearic 8 3 % lauric
3.0 g oleic 19.3 120 3.3 g 2.65 g

3.0 g stearic 8 0 % stearic 8 9 % oleic
1.0 g oleic 4.8 30 0.6 g 1.3 g

1.0 g linoleic 9 1 . 8 % oleic 5 7 % linoleic
2.6 g linoleic 13 79 1.4g

2.6 g linolenic 8 0 % linoleic
II. Lipids 41
c. Separation of saturated and unsaturated acids of natural oils

It is possible to bring about enrichment in the saturated and unsaturated acids
of natural oils. The acids or esters are recovered from the complexes by
warming the latter with ten times their weight of dilute hydrochloric acid. The
acids are extracted with petroleum ether and dried. The complex fraction is
enriched in saturated acids, while the noncomplex fraction is enriched in
unsaturated acids.
Fatty Acid of Urea (g) Methanol (ml) Complex (g) Noncomplex (g)
Olive oil, 50 g 50 150 13 37.7

Corn oil, 50 g 75 150 21 26
Soybean oil, 50 g 100 100 33.5 13.7
Linseed oil, 50 g 75 150 20 29
References
1. Schlenk, W. (1949). Ann. 565, 204.
2. Smith, A . E . (1950). / . Chem. Phys., 18, 150.
3. Schlenk, W. (1951). Ann. 573, 142.
4. Redlich, Ο., Gable, C. M., Dunlop, A . K . , and Millar, R . W. (1950). J. Am. Chem. Soc.
72, 4153.
5. Schlenk, W . , and Holman, R . T. (1950). / . Am. Chem. Soc. 72, 5001.
6. Zimmerschied, W. J . , Dimerstein, R . Α . , Wetkamp, A . W., and Marschner, R . F . (1950).
Ind. Eng. Chem. 42, 1300.
7. Knight, H. B . , Witnauer, L. P., Coleman, J . E . , and Swern, D . (1952). Anal. Chem. 24,
1331.
Recommended Reviews
1. Bishop, R . , and Dance, G. (1988). New types of helical canal inclusion networks. In "Topics
in Current Chemistry, 149, Molecular Inclusion and Molecular Recognition—Clathrathes
I I . " ( E . Weber, ed.), p. 137. Springer-Verlag, New York.
2. Schlenk, H. (1954). Urea inclusion compounds of fatty acids. In "Progress in the Chemistry of
Fats and Other Lipids" ( R . T. Holman, W. O. Lundberg, andT. Malkin, eds.), Vol. 2, p. 243.
Pergamon Press, London, England.
3. Swern, D . (1964). Urea complexes. In "Fatty Acids" (K. S. Markley, ed.), Vol. 3, p. 2309.
Interscience, New Y o r k .
4. Wosch, D . , and Vogtle, F . (1987). Separation of enantiomers by clathrate formation. In
"Topics in Current Chemistry, 140, Molecular Inclusion and Molecular Recognition—
Clathrates I . " ( E . Weber, ed.), p. 2 1 , Springer-Verlag, New York.
G. Gas-Liquid Chromatography of Methyl Esters of Fatty Acids

1. Introduction
Apart from the petroleum hydrocarbons, the fatty acids represent perhaps
the most complex group of naturally occurring substances, and until recently
no simple technique was available for their separation and identification.
Gas-liquid chromatography ( G L C ) was introduced by James and Martin in

1952 (1); they separated the normal saturated acids up to C 1 2 . This method
was extended by Cropper and Heywood (2) to the separation of C 1 2 - C 2 2 fatty
acids in the form of their methyl esters. Many methods have been described
for the preparation of methyl esters from fatty acids. The diazomethane
method (3) is rapid, but should not be used for polyenoic acids, as it also adds
to the double bond. Other procedures involve the use of methanol containing
a catalyst such as hydrochloric acid (4); hydrochloric acid and anion exchange
resin (5); and boron trifluoride (6). Orr and Callen (7) and Lipsky and
Landowne (8) used polyesters as liquid phases and obtained excellent separa-
tions of saturated and unsaturated esters. A complex mixture of polyenoic
acids was separated by Ackman, Burgher, and Jangaard (9). Oette and
Ahrens (10) have recommended the use of the relatively less volatile ß-
chloroethyl esters for C 2 - C 1 2 acids. Similarly, Craig, Tulloch, and Musty (11)
suggest the use of butyl, phenacyl, or decyl esters. The use of capillary
columns in preference to packed columns was suggested by Golay (12) and
used successfully by Lipsky, Lovelock, and Landowne (13) even for the
resolution of cis-trans isomers.
2. Principle
The great molecular range of naturally occurring fatty acids makes it impossi-
ble to carry out a comprehensive analysis of all constituents in a single run,
unless temperature or flow programming is used. The alternative approach,
e.g., the one described below (14), is to separate the mixture of esters on two
columns that have been adjusted to give optimal conditions for either stage.
Thus two stationary phases are used: 1,4-butanediol succinate for the low-
molecular esters; and diethylene glycol succinate for the high-molecular
esters.
3. Apparatus
Gas Chromatograph
4. Materials
1,4-Butanediol succinate Linoleic acid
Butyric acid Myristic acid
Caproic acid N-Nitrosomethylurea
Caprylic acid Oleic acid
Chromosorb Ρ Palmitic acid
Dichlorodimethylsilane Potassium hydroxide
Diethylene glycol succinate Stearic acid
Ether
II. Lipids 43
5. Time
5 - 6 hours
6. Procedure
a. Preparation of methyl esters

Twenty to thirty mg of the following acids are methylated with diazo-
methane: butyric, valeric, caproic, caprylic, myristic, palmitic, stearic, oleic,
and linoleic. An ethereal solution of the acids is treated with diazomethane,
which is prepared as follows: in a 50-ml round-bottomed flask are placed 6 ml
50% aqueous potassium hydroxide solution and 20 ml ether. The mixture is
cooled to 5°C, and 2 g nitrosomethylurea is added with shaking. The flask is
fitted with a condenser set for distillation. The lower end of the condenser
carries an adapter dipping below the surface of 5 ml ether contained in a
30-ml Erlenmeyer flask and cooled in an ice-salt mixture. The reaction flask
is placed in a water bath at 50°C and brought to the boiling point of the ether
with occasional shaking. The ether is distilled until it comes over colorless,
which is usually the case after two thirds of the ether has been distilled. Under
no circumstances should all the ether be distilled. The ether solution in the
receiving flask contains about 0.5 g diazomethane. If a dry solution of di-
azomethane is required, the ether solution of diazomethane is allowed to
stand for 3 hr over pellets of potassium hydroxide.
Warning! Diazomethane is not only toxic, but also potentially explosive.
Hence, one should wear heavy gloves and goggles and work behind a safety
screen or a hood door with safety glass. It is also recommended that ground
joints and sharp surfaces should not be used. Diazomethane solution should
not be exposed to direct sunlight or placed near a strong source of artificial
light.
b. Preparation of columns
U-shaped or coiled glass columns, 5 mm in diameter and 6 ft in length, are
used. The columns are treated with 5 % dichlorodimethylsilane in toluene,
washed with toluene and methanol, and dried. The partitioning medium used
for the esters of lower molecular weight is 1,4-butanediol succinate ( B D S )
in a ratio of 1:5 (w/w) on Chromosorb P, 60 to 80 mesh. For the esters of
higher molecular weight, diethylene glycol succinate ( D E G S ) is used in a
ratio of 1:5 (w/w) on Celite 545 (80 to 100 mesh) siliconized by treatment
with dichlorodimethylsilane. Columns are packed by gradual addition of the
coated support accompanied by repeated tapping. After packing, the columns
are preconditioned by baking for several hr at 200°C in a stream of nitrogen
with a flow rate of 50 ml per min.
c. Operating parameters
For the B D S column, the conditions are as follows: column temperature,
88°C; flash heater, 206°C; argon pressure, 17 psi; flow rate, 30 ml per min.
The conditions for the D E G S column are: column temperature, 180°C; flash
heater, 285°C; argon pressure, 41 psi; flow rate, 60 ml per min.
References
1. James, A . T . and Martin, A . J . P. (1952). Biochem. J. 50, 679.
2. Cropper, F . R . , and Heywood, A . (1953). Nature, 132, 1101.
3. Poper, R . , and Ma, T. S. (1957). Microchem. J. 1, 245.
4. Stoffel, W., Chu, F . , and Ahrens, Ε . Η. (1959). Anal. Chem. 3 1 , 307.
5. Hornstein, I . , Alford, J . Α . , Elliot, L. Ε . , and Crowe, P. Ε . (1960). Anal. Chem. 32, 540.
6. Metcalfe, L . D . , and Schnitz, A . A . (1961). Anal. Chem. 33, 363.
7. Orr, C. H., and Callen, J . E . (1958). / . Am. Chem. Soc. 80, 249.
8. Lipsky, S. R . , and Landowne, R . A . (1958). Biochim. Biophys. Acta 27, 666.
9. Ackman, R . G . , Burgher, R . D . , and Jangaard, P. M. (1963). Can. J. Biochem. Physiol.
4 1 , 1627.
10. Oette, K . , and Ahrens, Ε . Η. (1961). Anal. Chem. 33, 1847.
11. Craig, Β . M., Tulloch, A. P., and Murty, N. L. (1963). J. Am. Oil Chemists' Soc. 40, 61.
12. Golay, M. J . E . (1958). In: "Gas Chromatography" ( V . J . Coates, H. J . Noebels, and I. S.
Fagerson, eds.), p. 1. Academic Press, New York.
13. Lipsky, S. R . , Lovelock, J . E . , and Landowne, R . A . (1959). / . Am. Chem. Soc. 8 1 , 1010.
14. Vorbeck, M. L . , Mattick, L. R . , L e e , F . Α . , and Pederson, C. S. (1961). Anal. Chem.
33, 1512.
Recommended Reviews
1. James, A. T . (1960). Qualitative and quantitative determination of the fatty acids by gas-liquid
chromatography. In "Methods of Biochemical Analysis" ( D . Glick ed.), Vol. 8, p. 1. Inter-
science, New Y o r k .
2. Marcel, S. F . , and Lie Ken J i e . (1980). The characterization of long-chain fatty acids and
their derivatives by gas-liquid chromatography. Adv. Chromatogr. 18, 3.
3. Woodford, F . P. (1964). Gas-liquid chromatography of fatty acids. In "Fatty Acids" (K. S.
Markley, ed.), Vol. 3, p. 2249. Interscience, New York.
H. Thin-Layer Chromatography of Fatty Acids

I. Introduction
In a mixture of naturally-occurring fatty acids, differences in both chain
length and degree of unsaturation are usually encountered, and certain criti-
cal pairs of acids, e.g., oleic and palmitic, or linoleic and myristic, are insep-
arable on thin layers of various adsorbents. Such pairs were separated
by low-temperature thin-layer chromatography, by reversed-phase partition
chromatography on siliconized plates (1), and by bromination or hydrogéna-
tion of double bonds before chromatography.
Methyl esters of fatty acids may be separated, according to their degree
II. Lipids 45
of unsaturation, on silica gel plates impregnated with silver nitrate, by form-

ing a loose complex between silver ions and the electrons of double bonds
( 2 , 3 ) . An alternative method (outlined below) is the formation of adducts
with mercuric acetate (4). It was found that eis compounds react with mercu-
ric acetate 10 times quicker than trans compounds (5). When the adducts
are separated by thin-layer chromatography and decomposed with hydro-
chloric acid, the esters can be fractionated according to their chain lengths
by G L C .
In comparison with the method involving the use of mercuric acetate,
thin-layer chromatography on layers impregnated with silver nitrate has the
advantage of eliminating the stages of adduct-formation and the dissociation
of the separated adducts. Both methods are of great value when used in con-
jugation with G L C .
2. Materials
Acetic acid Mercuric acetate Petroleum ether
Chloroform Methanol fl-Propanol
Ethanol Methyl elaidate 5-Diphenylcarbazone
Ether Methyl oleate Silica gel G
Iodine Methyl stéarate Silver nitrate
3. Procedure
a. Preparation of plates
1. The suspension for five plates (20 x 20 cm) is prepared by shaking
30 g silica gel G and 60 ml water for 30 sec and applied uniformly to
a thickness of 0.25 mm with an applicator. After 30 min at room
temperature, the plates are heated in an oven at 125 to 130°C for
45 min.
2. After cooling, two plates are sprayed with concentrated aqueous
methanolic silver nitrate solution, 5 % relative to silica gel, and then
activated again at 120° for 30 sec. This method permits impregnation
of only part of the plate, which can thus be used for comparative
chromatography. The plates are used immediately after cooling.
b. Preparation of mercury addition compounds of unsaturated esters

The reagent consists of a solution of 14 g mercuric acetate in 250 ml metha-
nol, 2.5 ml water, and 1 ml acetic acid. Of this solution 25 ml is added to 1 g
methyl ester and allowed to react in a stoppered flask stored in the dark at
room temperature for 24 hr. Methanol is evaporated at 30°C under reduced
pressure or in a stream of nitrogen, and the dry residue is dissolved in 50 ml
chloroform. The chloroform solution is washed with 5 x 25 ml portions of
water to remove excess mercuric acetate, and dried on sodium sulfate.
c. Development
The samples are applied in chloroform solution along a line 2 cm above the
rim of the plate. To obtain optimal resolution, the solvent systems are applied
consecutively. First the saturated methyl esters (R/ = 0.9) are separated from
the acetoxy-mercurimethoxy derivatives of all unsaturated methyl esters
(Rf= 0.1) by means of a mixture of petroleum ether-ether ( 4 : 1 ) , within 1.5
to 2 hr. Then a mixture of n-propanol and acetic acid (100:1) is used to
separate, in the same direction, the acetoxymercurimethoxy derivatives of
unsaturated esters. This solvent is allowed to travel 3 - 4 hr.
d. Detection
After spraying with s-diphenylcarbazone in 9 5 % ethanol, the acetoxymercuri-
methoxy compounds appear as purple spots on a light rose background. The
esters of saturated acids are located as faint brown spots between the two
solvent fronts by exposing the chromatoplate to iodine vapors.
e. Plates impregnated with silver nitrate

Development of the esters is accomplished with ether-petroleum ether
( 5 : 9 5 ) . The spots are located by spraying with 5 0 % sulfuric acid and charring.
References
1. Malins, D . C , and Mangold, H. K. (1960). J . Am. Oil Chemists' Soc. 37, 576.
2. Morris, L. J . (1962). Chem. Ind. (London), 1238.
3. Bergelson, L. D . , Dyatlovitskaya, Ε . V . , and Voronkova, V . V . (1964). J . Chromatogr. 15,
191.
4. Mangold, H. K . , and Kammereck, R . (1961). Chem. Ind. (London) 1032.
5. Jantzen, E . , and Andreas, H. (1959). Ber. 92, 1427.
Recommended Reviews
1. Mangold, H. K. (1965). Aliphatic lipids. In Stahl, Ε . "Thin-layer Chromatography," p. 132,
2. Marcel, S. F . , and Lie Ken Jie. (1980). The characterization of long-chain fatty acids and
their derivatives by thin-layer chromatography. Adv. Chromatogr. 18, 35.
3. Nichols, B . W. (1964). The separation of lipids by thin-layer chromatography. Lab. Practice
13, 299.
I. Questions
1. What is the relationship between the degree of unsaturation of an oil

or fat and the melting point? Why must vegetable oils have lower
melting points than animal fats?
2. How are oils hydrogenated? What chemical and physical changes take
place?
III. Lignans 47
3. Discuss the factors operative in making a fat rancid.

4. What are the main applications of urea and thiourea complexes?
5. Why do most fatty acids contain an even number of carbon atoms?
6. Which products are obtained industrially from castor oil?
7. Outline some methods used for isolation and characterization of
natural lipids.
8. Why do only methyl groups appear as side chains in the natural
"branched" fatty acids?
J. Recommended Books
1. Deuel, H. J . (1957). "The Lipids" Interscience, New York.

2. Gunstone, F . D . (1958) "An Introduction to the Chemistry of Fats and
Fatty Acids " Chapman and Hall, London, England.
3. Hanahan, D . J . (1960). "Lipid Chemistry." John Wiley, New York.
4. Hilditch, T. P. (1956). "The Chemical Constituents of Natural Fats."
John Wiley, New York.
5. Markley, K. S. (1947). "Fatty Acids " Parts 1-4. Interscience, New
York.
6. Ralston, A. W. (1948). "Fatty Acids and Their Derivatives." John
Wiley, New York.
III. LIGNANS
A. Introduction
Compounds containing the following structural unit are abundant in nature.
Thus lignin is probably formed by the polymerization of a phenolic

phenyl-propane derivative to a complex cross-linked macromolecule. It has
been suggested that the key role is lignin formation is played to coniferin, the
glucoside of coniferyl alcohol.
Coniferyl alcohol
Natural phenolic resins (lignans) are closely related to lignin since they are
dimers of C 6 — C 3 units linked at the ß-position. A variety of forms is known,
including diarylbutane derivatives such as guaiaretic acid,
CH2 CH3O
2CH-CH3
OCH,
^CH-CH3
CH2
CH,C=CH OH
Guaiaretic acid
1,4-Diarylbutane derivative
and tetrahydrofuran derivatives such as olivil, lariciresinol, and sesamin,

which can be represented by the following structures:
Tetrahydrofuran derivatives
The majority of natural lignans possess the 4-hydroxy-3-methoxyphenyl

grouping seen in guaiaretic acid, olivil, and coniferyl alcohol.
Some lignans are sensitive to acids. Thus, olivil is converted into the
isomeric isoolivil, and lariciresinol, into isolariciresinol.
CH3O
CH,Q
HO^~^-CH 2 C H 2O H +
H
HO
OCH,
OH
Isolariciresinol
III. Lignans 49
Methylation and dehydrogenation reactions have made possible several cor-

relations within the lignan series. Thus methylation of sesamin converts it into
the dimethyl ether of pinoresinol.
Pinoresinol
Isoolivil can be dehydrogenated and converted into a lactone that can also be
obtained by dehydrogenation and subsequent methylation of conidendrin.
OH OH
Isoolivil Conidendrin
Lactone
Hydrogenolysis of galgravin gives rise to the formation of the dimethyl

ether of dihydroguaiaretic acid, while treatment with perchloric acid produces
a dihydronaphthalene derivative.
Dihydronaphthalene derivative
Many lignans are used as antioxidants, and others, as insecticides. The

essential feature of the biosynthesis of lignans is the oxidative coupling of
4-propenyl-phenols, such as coniferyl alcohol, at the /3-position of the C 3
chain.
B. Isolation of Sesamin and Sesamolin from Sesame Oil
Sesamolin
III. Lignans 51
1. Introduction
The seed oil of Sesamum indicum, commonly known as sesame oil, has two
minor constituents, sesamin and sesamolin. Three stereoisomers of sesamin
are known: sesamin, asarinin, and epiasarinin.
Sesamin was first isolated by Tocher from sesame oil in 1893 (1) and
later by Boeseken and Cohen (2). Sesamin has also been isolated from the
bark of various Fagaro species ( 3 ) , from Chamaecyparis obtusa ( 4 ) , from
Ocotea usambarensis (5), from the bark of Flindersia pubescens (6), and from
the fruit of Piper guineense (7). Unlike sesamin, sesamolin has not been noted
to occur in any genus other than Sesamum. Sesamin was isolated by molecu-
lar distillation of sesame oil (8). Details on how to obtain pure sesamin and
sesamolin by extraction from sesame oil have been reported by Halsam and
Haworth (9) and Beroza (10).
2. Principle
Sesame oil, which contains a large amount of glycerides, is passed through an
alumina column and eluted with petroleum ether (9). The fractions obtained
are examined by Badouin's color test for detection of lignans. Appropriate
fractions are collected, extracted with ether, and treated with alkali. Sesamin
and sesamolin are separated by fractional crystallization.
3. Apparatus
Column for chromatography
Soxhlet extractor
4. Materials
Acetic acid Ethanol Nitric acid
Acetic anhydride Ether Petroleum ether
Alumina Furfuraldehyde Potassium hydroxide
Chloroform Hydrochloric acid Sesame oil
Dioxane Methanol
5. Time
4 - 5 hours
6. Procedure
A glass column 10 cm in length and 3.5 cm in diameter is filled with 75 g
alumina in petroleum ether. 100 ml sesame oil is passed down the column and
eluted with petroleum ether, and the fractions collected are examined by
Badouins' test, which develops a deep red color in the aqueous phase when
the oil is shaken with concentrated hydrochloric acid and 2 % furfuraldehyde

solution. The portion immediately below the strong yellow band in the
column is removed and continuously extracted with ether in a Soxhlet appara-
tus for 3 hr. Removal of the solvents gives a yellow oil, which is saponified
with 5% alcoholic potassium hydroxide for 1 hr. Water (100 ml) is added, and
the soap solution is thrice extracted with 30-ml portions of ether. Removal of
the ether gives about 2 g yellow resin, which is dissolved in 10 ml ether and
left overnight, whereupon 0.5 g crystalline sesamin is precipitated. Crystal-
lization from ethanol yields rod-like needles of mp 122°C. The filtrate, after
removal of the ether, is dissolved in 1 ml chloroform, and petroleum ether
(80-100°C) is added until the onset of cloudiness. Sesamolin separates as a
white solid, which is crystallized from ethanol as white plates, mp 93-94°C;
yield, 0.1-0.15 g.
a. Nitrosesamin
A solution of 0.25 ml nitric acid (d = 1.4) in 3 ml acetic acid-acetic anhydride
( 2 : 1 ) is added over a period of 10 min to a solution of 1 g sesamin in 8 ml of
the same solvent, and the temperature is kept at 15 to 20°C. Dilution with
15 ml water gives a yellow gum that crystallizes from dioxane-methanol as
yellow needles of mononitrosesamin, mp 139-140°C, [ a ] D - 70°; yield, 0.4 g.
b. Sesamolin
1
c. H NMR [100 MHz]
a 8
53.2(q, J 8.5), 3.55(dd" J 8.0 and 8.5),
H-2 e_
5.43(s), 4.37(t, J 8.5)
4 H
3.88(dd, J 2.2 and 8.5), 6.65(d, J 8.8),
H H
4.07(dd, J 6.0 and 8.5) 6.44(dd, J 3.8 and 8.8),
H-5 H
2.85(m), 6.56(d, J 3.8)
4 . 2 8 ( d " j 5.5), 6.85 - 6 . 7 5 ( H a, , H b, , H c0

III. Lignans 53
d. Mass spectrum
Sesamolin C 2 0 H 1 8 O 7 , Mol. wt. 370.

+
m/z 3 7 0 ( M )
233
203
138
e. IR spectrum of ( + ) sesamin (in KBr)

- 1
2850 c m : sym. stretching of C H 2
1605, 1500, 1445: phenyl ring
1250: asym. stretching of = C — O — C
1200: in-plane bending of 1,2,4-substituted phenyl
1120, 1058: asym. stretching of cyclic ether C—O—C
930: most characteristic of methylenedioxy groups related to C—Ο
stretching
860, 800: out-of-plane C—Η bending, two adjacent hydrogen atoms
References
1. Tocher, J . F . (1893). Ber. 26, R 5 9 1 .
2. Boeseken, J . , and Cohen, W. D . (1928). Biochem. Z. 201, 454.
3. Carnmalm, B . , Erdtman, H., and Pelchowicz, Z . (1955). Acta Chem. Scand. 9, 1111.
4. Masumura, M. (1955). Nippon Kagaku Zasshi 76, 1318.
5. Carnmalm, B . (1956). Acta Chem. Scand. 10, 134.
6. Hollis, A . F . , Prager, R . H., Ritchie, E . , and Taylor, W. C. (1961). Australian J . Chem.
14, 100.
7. Hansel, R . , and Zander, D . (1961). Arch. Pharm. 294, 699.
8. Bhat, S. G . , Kane, J . G . , and Sreenivasan, A . (1956). J . Am. Oil Chemists' Soc. 33, 197.
9. Halsam, E . , and Haworth, R . D . (1955). / . Chem. Soc. 827.
10. Beroza, M. (1954). / . Am. Oil Chemists' Soc. 31, 302.
Recommended Reviews
1. Budowski, P. (1964). Recent research on sesamin, sesamolin and related compounds. J . Am.
Oil Chemists' Soc. 4 1 , 280.
2. Erdtman, H. (1955). Lignans. In "Modern Methods of Plant Analysis," (K. Paech, and
M. V . Tracey, (eds.), Vol. 3, p. 428. Springer-Verlag, New York.
3. Hearon, W. M . , and MacGregor, W. S. (1955). The naturally occurring lignans. Chem.
Revs. 5 5 , 957.
C. Questions
1. Define the terms lignan and lignin.

2. Classify lignans into their principal groups.
3. Describe the occurrence and structure of olivil and its transformation to
isoolivil.
4. What are the commercial uses of lignans?
5. Outline the biosynthesis of lignans.
D. Recommended Book
1. Dean F. M. (1963). "Naturally Occurring Oxygen Ring Compounds."

IV. QUINONES
A. Introduction
The quinones form a large group of natural pigments and are found mainly in
plants; many of them have also been isolated from microorganisms such as
fungi and lichens, and also from marine animals and certain insects. In gen-
eral, the quinones are yellow, red, or brown in color, but when present as
salts of hydroxy quinones, their colors are purple, blue, or green. The natural
quinones play a part in the oxidation-reduction processes of living matter,
and some of them have antibiotic properties. The naturally occurring
quinones are divided into the following groups:
1. Benzoquinones
These occur mainly in fungi and insects.
Fumigatin Spinulosin Aurantiogliocladin
Plastoquinone Ubiquinones (n = 6 - 10)

IV. Quinones 55
The most important benzoquinones produced by higher plants are the

ubiquinones (coenzyme Q) and plastoquinones.
2. 2,5-Dihydroxybenzoquinones
These occur principally in the higher fungi. Some mold products are diqui-
nones related to fumigatin and spinulosin.
Phoenicin Oosporein
3. Naphthoquinones
These are mostly isolated from plants.
Chimaphilin Phthiocol
OH
CH3
/
CH,CH=C
V
CH,
Lapachol
/CH3
CHOH-CH=C
\ CH,
Alkannin
Dunnione
The following are animal pigments:
OH Ο HO ο OH
HO CHCH3
H O " ^ ^ ^ ^ O H
OH Ο HO Ο
Echinochrome A Spinachrome A
CH,
/
CH,
CHXH=C
\ C16H33
Vitamin
4. Anthraquinones
This group is the largest. Many of these pigments occur in the Rubiaceae,
Polygonaceae, Rhamnaceae, and Leguminosae.
IV. Quinones 55
Tectoquinone Alizarin Rubiadin
Emodin
The best known insect pigment is carminic acid.
A more complex, extended anthraquinone, closely related to emodin, is

hypericin, which occurs in Hypericum species. It is formed by stepwise
intramolecular coupling.
HO Ο OH
Hypericin
Among the dianthraquinones, skyrin—a mold product—merits mentioning.
Skyrin
Although natural products related to phenanthrene are numerous, quinones

of this series are rare.
It is interesting to note that the quinones produced by insects are either

very simple or very complex, e.g., the aphin pigments. Thus, Aphis fabae
contains a yellow pigment that is converted by enzymes into an orange and
then a red compound, erythroaphin-fb. Zinc dust distillation of this com-
pound forms derivatives of perylene, benzoperylene, and coronene.
IV. Quinones 59
Erythroaphin-fb
Most of the natural quinones arise by the acetate-malonate pathway,

while the shikimic acid route is seldom utilized for quinone biosynthesis.
B. Isolation of Rhein from Rhubarb Root

1. Introduction
Rhein was first isolated from Chinese rhubarb in 1895 (1). It is present in
various Rheum species, partly in the free state and partly as a glycoside. It has
been isolated from the roots of Rheum palmatum (2), from senna leaves
{Cassia angustifolia) ( 3 ) , and from Cassia fistula (4). The antibiotic substance
cassic acid found in Cassia reticulata (5) has been identified with rhein. Other
natural sources of rhein are the roots of Rumex andreaeanum (6) and the
Brazilian species of Cassia alata, where it occurs mainly in a reduced glycosi-
de form (7).
Rhein
2. Principle
In the following experiment ( 5 ) , rhubarb root is extracted thoroughly with
water, concentrated in vacuo, and then extracted with methyl isobutyl
ketone. Rhein is recovered from the latter with sodium bicarbonate followed
by acidification.
3. Apparatus
Extractor
4. Materials
Acetic acid Methyl isobutyl ketone
Acetic anhydride Rhubarb roots
Acetone Sodium acetate
Hydrochloric acid Sodium hydrogen carbonate
5. Time
6-7 hours
6. Procedure
A batch of 100 g coarsely ground rhubarb root is placed loosely in a fluted
filter paper over a wad of glass wool in an extractor, and the active material is
extracted for three periods (1, 1.5, and 2.5 hr), using 750 ml water for each
extraction. The combined solution is concentrated under reduced pressure to
about 100 ml, and the syrupy concentrate is extracted with methyl isobutyl
ketone in a continuous extractor until the extract is almost colorless. The
organic solution is then shaken in a separatory funnel with small portions
(10-25 ml) of 5 % sodium hydrogen carbonate solution until the typical red-
dish color ceases to appear in the extracts. The aqueous alkaline extract is
cooled in ice and acidified to about pH 2 with cold, dilute hydrochloric acid,
and the tan amorphous precipitate is centrifuged, washed with water, and
dried in vacuo. The yield of crude rhein is about 200 mg. Previous removal of
dark pigment with acetone, followed by cold acetic acid, is necessary for
subsequent successful crystallization. The substance is crystallized from acetic
acid as pale yellow needles, mp 326-329°C.
a. Thin-layer chromatography of rhein

A drop of rhein solution (in chloroform) is spotted on a thin-layer plate (Silica
Gel GF254) and developed with ethyl acetate-methanol-water 8:1:1.
b. Detection U V 2 54 (after exposing the plate to ammonia vapors)

It reveals rhein as a red-violet spot, Rf 0.32, and, U V 3 65 as a pale orange spot.
c. UV spectrum of rhein
e OH
Aâ x 230 πιμ (logs 3.7); 260 (3.3); 430 (3.2)
Introduction of substituents into the anthraquinone nucleus, whose

absorptions are 252 πιμ (loge 4.68), 262 ιημ (loge 4.30), 272 m/x (loge 4.26),
323 πιμ (loge 3.26), and 410 χημ (loge 1.78), shifts the last band to longer
wavelengths.
IV. Quinones 61
d. Preparation of rhein diacetate

A solution of 100 mg rhein and 150 mg dry sodium acetate in 30 ml acetic
anhydride is refluxed for 15 min and poured into 175 ml ice water. The pale
yellow material is filtered and crystallized from acetic acid. Mp 250-251°C;
yield, 80 mg.
References
1. Hesse, O. (1895). Pharm. J . 1, 325.
2. Tschirch, Α . , and Eijken, P. A . A . F . (1905). Chem. Zentr. 76, 144.
3. Tutin, F . (1913). J . Chem. Soc. 103, 2006.
4. Modi, F . K . , and Khorana, M. L. (1952). Indian J . Pharm. 14, 6 1 .
5. Anchell, M. (1949). / . Biol Chem. Ill, 169.
6. Tsukida, K . , Yoneshige, M., and Tsujioka, J . (1954). J . Pharm. Soc. Japan 74, 382.
7. Hauptmann, Η., and Nazario, L. L. (1950). J . Am. Chem. Soc. 72, 1492.
Recommended Reviews
1. Sijnsma, R . , and Verpoorte, R . (1986). Anthraquinones in the Rubiaceae. Prog. Chem.
Org. Nat. Prod. 49, 79.
2. Thomson, R . H. (1957). Anthraquinones. In "Naturally Occurring Quinonesp. 158. But-
terworth, London, England.
3. Thomson, R . H. (1965). Quinones: Distribution and biosynthesis. In "Chemistry and Bioche-
mistry of Plant Pigments" (T. W. Goodwin, ed.), p. 309. Academic Press, New York.
C. Isolation and Identification of Phenols and Quinones from

Defensive Secretions of Beetles
1. Introduction
Among the arthropods, chemical defense substances play an important role in
the relationship of the organism to its predators.
Many tenebrionid beetles manufacture and store large quantities of
p-benzoquinones within their defensive glands ( 1 - 3 ) . The first mention of
tenebrionid defensive secretions are those of Gissler (4) and Williston ( 5 ) ,
who observed that seven species of Eleodes were able, upon being disturbed,
to eject a "pungent, vile-smelling liquid." Certain species of tenebrionids
have entered the folk literature as "circus bugs" from their conspicuous habit
of standing on their heads when disturbed.
In 1943 Alexander and Barton (6) reported the presence of ethyl-
quinone in the secretions of the flour beetle Tribolium castaneum. Tolu- and
ethylquinone were subsequently found in other tenebrionids: Diaperis macu-
lata (7), Eleodes hispilabris (8) and Eleodes longicollis (9). All three of these
reports indicated that hydrocarbons were also present in the defensive secre-
tions. They were identified from E. longicollis (10) as 1-nonene, 1-undecene
and 1-tridecene.
Quinones have also been found in the secretions of several species of

Blaps (11), Tenebrio molitor (12), Alphitobius diaperinus (13), Zophobas
rugipes (14) and Blaps sulcata and Blaps wiedemanni (15).
It has been suggested that the quinones are generated from phenol
glucosides by hydrolysis and subsequent oxidation (16).
The Central American tenebrionid beetle, Zophobas rugipes, has a pair
of prothoracic defensive glands secreting phenols and a pair of abdominal
defensive glands secreting quinones (17). It has been assumed that the phenol
precursors are probably oxidized to quinones.
An interesting mechanism (see Fig. 3) has been proposed for the gen-
eration of quinones from phenols in the defensive organ of the bombardier
beetle.
Figure 1.3 Defensive organ of the bombardier beetle.

IV. Quinones 63
2. Principle
Blaps, flour beetles, or any other tenebrionids can be obtained from entomo-
logical laboratories. The pungent secretion of the quinones is obtained by
slightly pressing the body of the insect. It is collected with fine capillaries and
analyzed by chromatographic ( T L C ) and spectroscopic (NMR, I R , M S )
methods. Care should be taken when handling these lachrymatory and skin
irritating compounds!
The following procedure is based on (15).
3. Apparatus
Infrared spectrophotometer
Mass spectrometer
Nuclear magnetic resonance spectrometer
4. Materials
Blaps
/?-Benzoquinone Glass capillaries
Carbon disulfide Hydroquinone
2,4-Dinitrophenylhydrazine a-Naphthol
Flour beetles
5. Time
3 hours
6. Procedure
a. Collection of secretion
Pressing the body of Blaps causes the discharge of pungent, yellowish-brown
liquid, which is collected with the help of fine capillaries and stored in a
deep-freeze refrigerator. The secretion consists of two phases, aqueous and
hydrophobic. The nonaqueous phase is soluble in carbon disulfide.
The C S 2 solution is subjected to various chromatographic and spectros-
copic studies, whereas the aqueous phase serves for the identification of
glucose.
b. TLC of the secretion

The crude secretion (or its C S 2 solution) is spotted on a silica gel G F 2 5 4 plate
(0.25 mm thick) and developed with petrol-ether-ether, 7 : 3 . The quinones
and hydroquinones are detected with the help of U V light (254 nm) and by
spraying with 2,4-dinitrophenylhydrazine solution and chloranil reagent,
(prepared by dissolving 0.5 g chloranil in 10 ml methanol).
Separation and Identification of Quinones and Hydroquinones by TLC
Zone on
0
Chromatogram Compound Rf Visible 2,4-DNP Chloranil Reagent
A Hydroquinone 0.12 — — Blue

Β 2-Methyl hydroquinone 0.14 — — Blue
C 2-Ethyl hydroquinone 0.16 — — Blue
D p-Benzoquinone 0.48 Yellow Orange-brown —
Ε 2-Methyl benzoquinone 0.53 Yellow Orange-brown —
F 2-Ethyl benzoquinone 0.66 Yellow Orange —
α
All compounds absorb at U V (254 nm) light.
c. Quinones and hydroquinones
Infrared Spectra of Benzoquinones (in C S 2)
Absorption (u) Characteristic of
6.05 Carbonyl group

9.2 and 12.35 2-methyl-l,4-benzoquinone
11.02 and 12.0 2-ethyl-l,4-benzoquinone
Ultraviolet Spectra
H
Compound Am£ (nm)
1,4-Benzoquinone 242
2-Methyl-l,4-benzoquinone 245
2-Ethyl-1,4-benzoquinone 247
Hydroquinone 292
2-Methyl hydroquinone 293
2-Ethyl hydroquinone 294
d. Mass spectra
The following molecular ions are 136, 122 and 108, and correspond to ethyl-,
methyl- and benzoquinone, respectively.
The following is a fragmentation scheme of benzoquinone:
IV. Quinones 65
1
H-NMR
α
Quinone Structural Unit δ
(ppm)
6.75 (s)
"H
(a) 6.58 (m)

(b) 6.70 (s)
2.01 (d)
(a) 6.58 (m)

(b) 6.70 (s)
2.45 (q)
1.16 (t)
a
Values (in C S 2 ) refer to tetramethylsilane (5 = 0 ) . Letters in
parentheses refer to doublet (d), multiplet ( m ) , quartet ( q ) , singlet
(s), and triplet ( t ) .
References
1. Schildknecht, H. (1963). Angew. Chem. 75, 762.
2. Eisner, T . , and Meinwald, J . (1966). Science 153, 1341.
3. Weatherston, J . (1967). Quart. Rev. Chem. Soc. Lond. 2 1 , 267.
4. Gissler, C. G . (1879). Bull. Brooklyn Ent. Soc. 2, 7.
5. Willistton, S. W. (1884). Psyche, Camb. 4, 168.
6. Alexander, P., and Bartton, D . H. R . (1943). Biochem. J. 37, 463.
7. Roth, L . M . , and Stay, B . (1958). / . Insect Physiol. 1, 305.
8. Blum, M. S., and Crain, R . D . (1961). Ann. Ent. Soc. Am. 54, 474.
9. Chadha, M. S., Eisner, T . , and Meinwald, J . (1961). J. Insect Physiol. 7, 46.
10. Hurst, J . J . , Meinwald, J . , and Eisner, T. (1964). Ann. Ent. Soc. Am. 57, 44.
11. Schildknecht, H., and Weis, Κ. Η. (1960). Ζ. Naturf. 15b, 757.
12. Schildknecht, Η., and Kramer, Η. (1962). Ζ. Naturf. 17b, 701.
13. Tseng, Y . L . , Davidson, J . Α . , and Menzer, R . E . (1971). Ann. Ent. Soc. Am. 64, 425.
14. Tschinkel, W. R . (1969). / . Insect Physiol. 15, 191.
15. Ikan, R . , Cohen, E . , and Shulov, A . (1970). / . Insect Physiol. 16, 2201.
16. Eisner, T . , McHenry, F . , and Salpeter, M. M. (1964). J. Morph. 115, 355.
17. Tschinkel, W. R . (1969). / . Insect Physiol. 15, 197.
Recommended Reviews
1. Weatherston, J . (1967). The chemistry of arthropod defensive substances. Quart. Rev.
Chem. Soc. 2 1 , 2 8 7 - 3 1 3 .
2. Weatherston, J . , and Percy, J . E . (1970). Arthropod defensive secretions. In ''Chemicals
Controlling Insect Behavior." (M. Beroza, ed.), 287-313 Academic Press, New York.
D. Questions
1. What are the functions of quinones in nature?
2. Outline the biosynthesis of quinones.
3. Describe methods of isolation and identification of lapachol and skyrin.
E. Recommended Books
1. Morton, R. A. (ed.) (1965). "Biochemistry of Quinones." Academic
Press, New York.
2. Thomson, R. H. (1957). "Naturally Occurring Quinones."
3. Patai, S., and Rappoport, Z. (eds.) (1988). "The Chemistry of
Quinonoid Compounds" Wiley, New York.
V. PHLOROGLUCINOLS
A variety of natural products contain the phloroglucinol nucleus in their
structure. It can be regarded as derived from three acetate units.
Ο
II
As indicated above, phloroglucinol can be represented as a tautomeric

triketone, and many reactions of phloroglucinol derivatives are best under-
stood by reference to this ketonic structure.
The bitter substances found in hops (Humulus lupulus) have isoprenoid
side chains attached to the phloroglucinol nucleus or to a cyclopentatrione
ring. In view of the well-known anionoid activity of the phloroglucinol nu-
V. Phloroglucinols 67
cleus, it is considered that the introduction of the acyl side chains such as
C O C H 2 C H ( C H 3 ) 2 of humulone may occur through the isopentenyl cation
+
( C H 3 ) 2 C = C H - C H 2 . Plants containing compounds possessing a phlorogluci-
nol moiety have been used as antihelminic drugs, and many of them possess
insecticidal and bacteriocidal properties.
A. High-Performance Liquid Chromatography of

Hop Bitter Substances
1. Introduction
The flavor of beer, like that of many foods and beverages, is composed of
many volatile and nonvolatile compounds present in a definite blend.
Principal classes of volatiles of beer are acetals, acids, alcohols, alde-
hydes, amides, amines, esters, furans, hydrocarbons, ketones, lactones, phe-
nols, pyrazines, pyridines.
Modern separation and identification techniques place the number (of
volatile and nonvolatile compounds in beer) close to 800. Only a small num-
ber of these compounds are "flavor active."
The hop plant (Humulus hupulus) is a climbing herbaceous plant be-
longing to the natural family Moraceae and the natural order of Urticales.
The lupulin glands secrete the bitter resin and essential oil at the base of the
female flowers.
The resin fraction of hops consists of two major groups of compounds,
the α-acids (humulenes) and β-acids (lupulones), which together normally
form 1 0 - 1 5 % of the weight of the dried hops. These compounds are of mixed
biogenetic origin and may be regarded as phloracylphenones, modified by
introduction of isopentenyl side-chains and derived biogenetically from the
desoxy α acids.
Both the α and β acid fractions of hops consist of a mixture of homologs
in which the structure of the acyl side-chain varies. The proportionate com-
position of the α and β acid fractions varies widely with the variety of hop.
Thus European hops generally contain large quantities of humulone in rela-
tion to the other homologs, whereas American and Japanese varieties fre-
quently contain almost as much cohumulone as humulone. These differences
may be quite significant, since cohumulone is normally better utilized in the
brewing process and may give rise to less desirable flavor characteristics than
humulone.
In the brewing of beer, hops are boiled with malt and other cereal
extracts (wort) in the brew kettle for a given period. During this period, the
three major hops α-acids (I) humulone, cohumulone and adhumulone and
the minor ß-acids (II) undergo heat-induced isomerization into iso-a-acids
(III) (each α-acid yields a cis-trans pair of stereoisomers), and hulupones (IV).
Beer therefore contains six major bitter iso-a-acids. Quantitation of

these compounds in isomerized hop extracts, worts, and beers is very impor-
tant in the brewing industry. Various HPLC methods have been used ( 1 - 3 )
for separating the bitter principles of hops.
Ill IV
R = C H 2C H ( C H 3) 2 : humulone (I) and lupulone (II)
R = C H ( C H 3) 2 : cohumulone and colupulone
R = C H ( C H 3 ) C H 2 C H 3 : adhumulone and adlupulone
2. Principle
In the following procedure ( 4 ) , the beer extract is analyzed by the HPLC
technique using sodium acetate-acetic acid-buffer-methanol-water eluant.
Addition of B H T (butylhydroxy toluene), a well-established antioxidant, to
the eluting solvent and to the extract improves the results.
3. Apparatus
HPLC apparatus
Lichroma tubing packed with C 1 8 silica gel
Syringe
4. Materials
Acetic acid Isooctane
Beer Methanol
BHT Sodium acetate
V. Phloroglucinols 69
5. Procedure
Beer (20 g) is weighed into a beaker and then transferred with minimal
foaming into a 100 ml separation funnel, acidified with 2 ml 3N HCl and
extracted with 2 portions (25 ml each) isooctane. Twenty-five ml of the
isooctane layer is completely evaporated in a rotavapor. HPLC of the hop
acids is performed on a polar octadecyl ( C 1 8 ) phase, which was treated with
silica gel (10 μπι), treated with octadecyltrichlorosilane and containing ca.
17% bonded organic material. The column is 25 x 0.46 cm Lichroma tubing.
Elution is carried out with the following elution system: methanol-water-
acetic acid ( 8 5 : 1 5 : 1 ) . Addition of B H T to the sample solution ( 1 % ) and to
the eluting solvent ( 1 % ) improves the results.
The order of elution of the hop acids is cohumulene, adhumulene,
humulone, colupulene, and lupulone.
References
1. Verzele, M., and Dewaele, C. (1981). J. Chromatogr. 217, 399.
2. Anderson, B . (1983). J. Chromatogr. 262, 448.
3. Knudson, E . , and Siebert, K. (1983). J. Am. Soc. Brew. Chem. 4 1 , 5 1 .
4. Verzele, M., and de Potter, M. (1978). J. Chromatogr. 166, 320.
Recommended Reviews
1. Birch, A . J . (1957). Biosynthetic relations of some natural phenolic and enolic compounds.
Prog. Chem. Org. Nat. Prod. 14, 186.
2. Ashurst, P. R . (1967). The chemistry of hop resins. Prog. Chem. Org. Nat. Prod. 25, 63.
3. Charalambous, G. (1981). Volatile constituents of beer. In "Brewing Science, 2 . " ( J . R . A .
Pollock, ed.), p. 167. Academic Press, New York.
4. American Society of Brewing Chemists. (1976). "Methods of Analysis." St. Paul, New Y o r k .
5. "Brewing Science." Verzele, M., and Pollock, J . , eds. (1979). Academic Press, New Y o r k .
6. Meilgaard, M. C , and Peppard, T . L. (1986). The flavour of beer. In "Food Flavours,
Part B , " p. 99. Elsevier, Amsterdam.
CARBOHYDRATES
I. MONO- AND OLIGOSACCHARIDES

A. Introduction
The carbohydrates are among the most abundant constituents of plants

and animals. In plants they constitute the membranes of the cell walls.
They can be divided into the following classes: monosaccharides, e.g.,
arabinose, C 5 H i 0 O 5 , glucose, C 6 H 1 2 0 6 ; oligosaccharides, e.g., sucrose,
C12H22O11, raffinose, C 1 8 H 3 2 0 1 6 ; and polysaccharides, e.g., starch, cellu-
lose [ ( C 6 H 1 20 6 ) „ - ( « - l ) H 2 0 ] .
1. Monosaccharides
The monosaccharides are polyhydroxyaldehydes or polyhydroxyketones and
are classified according to the length of the carbon chain and the nature of
the carbonyl group. The following are examples of tetroses, pentoses, and
hexoses (both "aldoses" and "ketoses").
CHO
CHO C H 2O H H—C—OH
H—C—OH c=o H—C—OH
H—C—OH H—C—OH H—C—OH
C H 2O H C H 2O H C H 2O H
D-Erythrose D-Erythrulose D-Ribose
70
I. Mono- and Oligosaccharides 71
CHO CH 2 0H
I I
CH 2 0H H-C-OH C==O
I I I
C=O HO-C-H HO-C-H
I I I
H-C-OH H-C-OH H-C-OH
I I I
H-C-OH H-C-OH H-C-OH
I I I
CH 2 0H CH 2 0H CH 2 0H
D-Ribulose D-Glucose Fructose
Heptoses are found in certain plants and bacteria. For example, L-

glycero-D-mannoheptose has been isolated from the cell walls of Escherichia
coli, and sedoheptulose from the avocado pear.
CHO CH 2 0H
I I
HO-C-H C=O
I I
HO-C-H HO-C-H
I I
H-C-OH H-C-OH
I I
H-C-OH H-C-OH
I I
HO-C-H H-C-OH
I I
CH 2 0H CH 2 0H
L-Glycero-D- mannoheptose Sedoheptulose
Their importance in the photosynthetic carbohydrates was recently demon-

strated by Calvin and his coworkers.
The consensus is that the steric structure of a sugar is related to the two
antipodes of glyceraldehyde.
CHO CHO
I I
H-C-OH HO-C-H
I I
CH 2 0H CH 2 0H
D-Glyceraldehyde L-Glyceraldehyde
Thus the configuration of the Hand OH groups on the lowest asymmetric

carbon atom (next to the -CH 2 0H group) of a sugar indicates whether the
sugar is derived from D- or L-glyceraldehyde.
72 CHAPTER 2 Carbohydrates
CHO CHO
H—C—OH HO—C—H
HO—C—H HC—OH
C H 2O H C H 2O H
D-Glucose L-Glucose
The mirror images of a sugar ( L and D ) are called optical antipodes or

enantiomorphs. They have identical chemical and physical properties and
differ only in the sign of their optical rotation.
It is noteworthy that the structures of glucose and mannose contain four
asymmetric, identical groups, except for those at C 2 , which are opposite in
space. Such isomers are called epimers.
CHO CHO
I
I
HO—C—H HO—C—H
H—C—OH H—C—OH
I H—C—OH
H—C—OH C H 2O H
Mannose
C H 2O H
Another group of monosaccharides are the deoxy-sugars, e.g., 2-deoxy-
Glucose
D-ribose, found in D N A , or colitose, a 3,6-dideoxy hexose isolated from
bacterial lipopolysaccharides.
CHO CHO
I
H—C—H HO—C—H
I
H—C—OH
I
I CH2
H—C—OH
H—C—OH
C H 2O H HO—C—H
2-Deoxy-D-ribose I
CH3
Colitose
Streptose from streptomycin and apiose from parsley are examples of

branched-chain sugars.
CHO
H—C—OH CHO
O, I
C—C—OH
H—C—OH
H
HO—C—H
HO.HC CH,OH
CH3 OH
L-Streptose D-Apiose
As alcohols, carbohydrates form esters. The phosphoric esters of

pentoses and hexoses are of great physiological importance, the former as
CH,OP
POCH 2 η Ç H 2O H
hexokinase phospho-hexokinase
Starch
OH
HO OH OH
OH OH
Glucose-6-phosphate Fruciose-6-phosphate
C H 2O P
I
c=o CH,OP C H 2O P CHO
I
HO—C—H
aldolase -2H I dehydrogenase
I c=o CHOH CHOH
H—C—OH
C H 2O H I
I
H—C—OH C H 2O H
C H 2O P
Dihydroxyacetone 3-Glyceraldehyde
I phosphate phosphate
C H 2O P
Fructose-1,6-diphosphate
COOH COOH COOH COOH

I phosphoglycerom utase - H 20 I ATP co-carboxylase
CHOH CHOP enolase COP c=o
I C H 2O H CH2 CH3
C H 2O P 2-Phosphoglyceric Phosphoenol Pyruvic acid
3-Phosphoglyceric
acid pyruvic acid
acid
CHO
+ DPNH2
I + co 2
C H 3C H 2O H
CH3 Ethyl alcohol
Acetaldehyde
constituents of nucleic acids and the latter as prerequisites for fermenta-

tion—the biological breakdown of carbohydrates.
The accepted scheme (proposed by Embden-Meyerhof) for the fer-
mentation of starch to ethyl alcohol is shown on the previous page.
If any interference occurs at the final stage (e.g., by addition of sulfite),
then reduced diphosphopyridine nucleotide (DPNH 2 ) will hydrogenate the
dihydroxyacetone phosphate, forming glycerol.
A number of other fermentations are known, such as the acetone-
butanol fermentation caused by Clostridium acetobutylicum Weizmann or
that of lactose into lactic acid by Streptococcus lactis.
Treatment of aldo- and keto-sugars with methanol containing hydro-
chloric acid yields two isomeric methyl glycosides, which differ only in the
configuration at Q . These epimers are called anomers.
H OCH, CH H
C
I
H-C-OH
H-C-OH
HO-C-H ο O
HO-C-H
H-C-OH
I H-C-OH
H-C H-
C
ι C H 2O H
C H 2O H
Methyl α-D-glucoside Methyl ß-D-glucoside
It has been demonstrated that the free monosaccharides also exist in

two forms that are structurally related to methyl glucosides. The ririg may
be five-membered—a derivative of tetrahydrofuran (furanose), or six-
membered—a derivative of pyran (pyranose).
CH,OH
C H 2O H
OH OH
H OH H OH
a-D-Glucopyranose a-D-Glucofuranose
As in the case of the cyclohexane series, in which the equatorial substi-

tuent of the chair form is more stable than the axial one, pyranose rings also
show a preference for the chair form and the substituent (CH 2 OH in this case)
occupies the equatorial position.
R H
C H 2O H
HO
OH
H
C H 2O H equatorial C H , O H axial
In aqueous solution, sugars undergo changes in optical rotation—

mutarotation; one isomeric form is probably transformed into the other via an
aldehydic form.
C H 2O H CH,OH C H 2O H
OH 0 = C - H
vOH
HO^
H
fn
H OH H OH Η OH
/?-D-Glucopyranose Aldehydic form a-D-Glucopyranose
On degradation of pentoses with strong acids, 2-furfuraldehyde is

formed, whereas hexoses form 5-hydroxymethyl-2-furfuraldehyde.
^cr CHO H O H 2C ^ ^ O ^ " C H O

2-Furfuraldehyde 5-Hydroxymethyl-2-furfuraldehyde
In alkaline solution, the monosaccharides are unstable and undergo a

variety of transformations, e.g., the Lobry de Bruyn reaction, whereby glu-
cose is converted into fructose and mannose.
Phenylhydrazine and other substituted hydrazines are important in the
identification of the various monosaccharides. When one mole of phenyl-
hydrazine reacts with one mole of an aldose or ketose, the product is a
normal hydrazone. On treating it with an excess of Phenylhydrazine, an
osazone is formed. Hydrolysis of the osazone with hydrochloric acid yields

the corresponding osones, which are polyhydroxy-2-keto-l-aldehydes.
CHO C H = N N H C 6H 5 C H = N N H C 6H 5 H—C=0
CH
CHOH 6 s N H N H 2) C HH O C 6 H 5 N H N H 2) Q^NHQf^ JIÇ^ ( L = Q
R R R R
Hydrazone Osazone Osone
It should be noted that the osazones formed from glucose, mannose,

and fructose are identical, hence the lower carbon atoms ( C 3 — C 6 ) of these
three sugars have identical configurations.
Several methods have been devised for shortening the chain of an aldose
by one carbon atom: Wohl's, Ruff's, and Weerman's. Procedures used for
lengthening the chain of an aldose are those of Killiani and Sowden.
Both aldoses and ketoses may be reduced to the corresponding polyhy-
droxy alcohols. Oxidation of aldoses with a variety of reagents gives dibasic
acids, e.g., saccharic acid.
2. Oligosaccharides
The oligosaccharides are classified as di-, tri-, tetra-, etc., saccharides depend-
ing upon the number of monosaccharides produced upon acid hydrolysis.
Substances composed of up to ten monosaccharide molecules are included in
the group of oligosaccharides. The monosaccharide units may be identical, as
C H 2O H OH
Q -0-1
OH >H,OH
vOH
N
HO 0
OH C H 2O H
Cellobiose
C H 2O H [-OCH2 Η,ΟΗ
- ο o -
vOH HO/
HO )H
OH OH
Gentiobiose
in maltose, or different, as in sucrose. If the Q hydroxyl groups of compo-

nents (of a disaccharide) are linked to each other, the disaccharide is nonre-
ducing (sucrose and trehalose); if the union occurs in such a way that only one
of the hydroxyl groups participates, then reducing disaccharides are formed,
e.g., cellobiose or gentiobiose.
Rafiinose is an example of a naturally occurring trisaccharide.
H OH
k |—O—CH
OH H\ _ H HOCH
OH H/
CH,OH HO CH,OH
OH OH H
Rafiinose
Amino sugars such as glucosamine and galactosamine are abundant in

nature. They are obtained by hydrolysis of animal polysaccharides such as
chitin and heparin, and can, of course, also be synthesized.
CH,OH CH,OH
HO
HOH Η,ΟΗ
HO
NH2 NH,
D-Glucosamine D-Galactosamine
3. Glycosides
Plant glycosides are found in leaves, seeds, and bark of trees. They are
crystalline, sometimes bitter solids. The glycosides can be hydrolyzed by
enzymes or by acids; the noncarbohydrate moiety is called aglycone. The
phenolic glycoside, arbutin, is found in pears, salicin in willow bark, phlorid-
zin in the bark of plum and apple trees, and coniferin in pine trees.
Salicin
OH
Phloridzin
Many pigments, such as those of the flavone and anthocyanin series, are
of glycosidic nature. Dyestuffs such as alizarin and indigo are obtained by
hydrolysis of ruberythric acid and indican, e.g., indican is hydrolyzed to
indoxyl, which is then oxidized to indigo.
Ruberythric acid
CH,OH
Mustard oil glycosides, such as sinigrin, liberate the pungent mustard

oils, e.g., allyl isothiocyanate, when the seeds are crushed in the presence of a
plant enzyme.
^/OSOjK
C H 2= C H C H 2N = C • C H 2= C H C H 2N = C = S + K H S 0 4
scr^ u r\ Allyl isothiocyanate
Sinigrin
The cardiac glycosides, such as oleandrin, are used in medicine for

stimulating the heart muscle. Their sugars are mostly deoxysugars, e.g.,
cymarose and diginose.
Oleandrin D-Cymarose D-Diginose
Saponin glycosides such as tigonin form a soapy foam on mixing with

water, and are toxic. On hydrolysis they yield sapogenin and a sugar, com-
posed of five sugar units (2 glucose, 2 galactose, and 1 xylose).
Tigonin
B. Isolation of D-Mannoheptulose from Avocado
1. Introduction
The first seven-carbon sugar to be discovered in nature was D-manno-
heptulose, whose isolation from the avocado was announced by La Forge
in 1917 (1).
The sugar is accompanied by the closely related heptitol, perseitol, and
also by very small quantities of the related eight-carbon compounds, D -
glycero-D-mannooctulose and D-erythro-D-galacto-octitol (2). D-Manno-
heptulose has also been isolated from fresh avocado leaves (3). Avocado
varieties differ greatly in their D-mannoheptulose content. In all cases, the
fruit is picked green and allowed to ripen in storage; the D-mannoheptulose

content does not vary under these conditions.
C H 2O H
c=o
I
HO—C—H
I
HO—C—H
I
H—C—OH
H—C—OH
C H 2O H
D-Mannoheptulose
2. Principle
According to the following procedure (4), the pulp of avocado is extracted
with 2 0 % aqueous ethanol and freed from most oil by adding Celite and
filtering. The aqueous solution is then deionized by passing it through cationic
and anionic ion-exchange resins. Concentration of the effluent leaves a thin
syrup consisting of a mixture of perseitol and mannoheptulose, which are
fractionally separated by seeding the methanolic solution first with perseitol
and then with mannoheptulose. D-mannoheptulose is further purified by
forming a hexacetate (5).
3. Apparatus
Columns for chromatography
Polarimeter
4. Materials
Acetic anhydride Ethanol
+
Amberlite I R - 1 2 0 [ H ] Ether
Avocado Methanol
Celite Perseitol
Chloroform Pyridine
Duolite A - 4 [ΟΗΓ] Sodium hydrogen carbonate
5. Time
Isolation: 5 hours
Crystallization: 2 days
6. Procedure
Avocados are quartered and peeled, the pulp is crushed and mixed thor-
oughly with about half its weight of 2 0 % aqueous ethanol to make a thin
soup, and the mixture is heated for 4 hr at 60°C to coagulate the pulp. The
mixture is filtered through a large Büchner funnel, and the pulp is reextracted
with 2 0 % ethanol in the same manner. The combined filtrates are freed from
any oil that has separated by mixing with Celite and filtering through a
Büchner funnel. The solution is concentrated under reduced pressure to a
thin syrup, which is poured, with stirring, into 8 volumes of methanol. The
precipitated gum separates as small flakes and is filtered off and washed with
methanol-water, 8 : 1 . The filtrate is concentrated under reduced pressure to
remove the methanol, and the residual aqueous solution is deionized by
passing it through columns of suitable ion-exchange resins, e.g., Amberlite
+ -
I R - 1 2 0 [ H ] and Duolite A - 4 [ O H ] . The effluent is concentrated under
reduced pressure to a thin syrup, which is dissolved in 4 volumes of methanol
and seeded with perseitol. The product is allowed to crystallize for several
days at room temperature. Perseitol separates as white needles and is filtered
off and washed with 8 0 % methanol. The filtrate is concentrated under re-
duced pressure to a thick syrup, which is dissolved in methanol, seeded with
perseitol, and cooled in the refrigerator. If more perseitol separates, the
material is filtered off, and the filtrate is concentrated and redissolved in
methanol. When no further crystallization of perseitol can be induced, the
solution is seeded with D-mannoheptulose, which separates as relatively
large, transparent prisms. Purified by recrystallization from methanol, D -
mannoheptulose melts at 151 to 152°C; [ a ] ^ + 29° (water). By way of com-
parison, perseitol melts at 187 to 188°C; [α]ο - 1° (water). The relative yields
of the two sugars differ from one variety of avocado to another.
a. D-Mannoheptulose hexaacetate
Acetylation of 1 g pure, crystalline D-mannoheptulose is accomplished by
dissolving the sugar in 5 ml acetic anhydride and 5 ml dry pyridine at 0°C. The
solution is kept at this temperature for 48 hr and then poured into several
times its volume of ice and water. The acetate is extracted with chloroform;
the extract is washed with cold dilute sodium hydrogen carbonate and then
with water until free of acetic acid and pyridine. The washed chloroform
solution is dried and then concentrated under reduced pressure until free of
solvent. The syrup crystallizes readily; the acetate may be recrystallized from
warm ether as large prisms. It has a mp of 110°C; [α]ο + 39° (chloroform).
References
1. La Forge, F . B . (1917). J. Biol. Chem. 28, 511.
2. Charlston, A . J . , and Richtmyer, Ν. K. (1960). J. Am. Chem. Soc. 82, 3428.
3. Nordal, Α . , and Benson, A . A . (1954). J. Am. Chem. Soc. 76, 5954.
4. Richtmyer, Ν. K. (1962). Methods Carbo. Chem. 1, 173.
5. Montgomery, Ε . M. (1962). Methods Carbo. Chem. 1, 175.
Recommended Reviews
1. Ahmed, Ε . M . , and Barmore, C. R . (1980). Avocado. In "Tropical and Subtropical Fruits."
(S. Nagy and P. E . Shaw, eds.), p. 121. Avi Publishing, Westport, Connecticut.
2. Webber, J . M. (1962). Higher carbon sugars. In "Advances in Carbohydrate Chemistry."
(M. L. Wolfrom, and R . S. Tipson, eds.) Vol.15, p. 15. Academic Press, New York.
C. α-D-Glucosamine from Crustacean Shells
1. Introduction
Chitin is a poly glucosamine and is widely distributed in invertebrates. The
occurrence of chitin in the plant kingdom is confined to fungi and green algae.
Because of their ready availability and low protein content, decalcified shells
are the most suitable source of chitin. Crab and lobster shells are commonly
employed and are available commercially.
2-Amino-2-deoxy-D-glucose hydrochloride can be isolated by the hy-
drolysis of crude chitin with hot concentrated hydrochloric acid. The crys-
talline hydrochloride was first prepared by Ledderhose from a lobster shell
hydrolyzate (1). Treatment of the hydrochloride with strong bases, such as
diethylamine or triethylamine, gives free D-glucosamine ( 2 , 3 ) .
C H 2O H NHAc Ç H 2O H Η NHAc
Q rΟ x
Ή OH H Ή,OH HCl
Η
H NHAc CH,OH
Chitin
CH,OH
çm
H O H
H/
HO
H NH2
a-D-Glucosamine
2. Principle
In the following procedure (4) crab shells are cleaned and decalcified by
digestion with dilute hydrochloric acid, thus yielding crude chitin.
Degradation of chitin is accomplished by heating with concentrated
hydrochloric acid. Crude glucosamine hydrochloride is purified by filtration
through Celite and activated carbon. Final purification is effected by dissolv-

ing the product in hot water and adding ethanol, whereupon the a-anomer
crystallizes while the /3-isomer remains in the solution.
3. Apparatus
Evaporator
4. Materials
Celite Ether
Crab shells Hydrochloric acid
Ethanol, 9 5 % Triethylamine
Ethanol, absolute
5. Time
Decalcification of shells: 12 hours
Preparation of glucosamine hydrochloride: 4 hours
6. Procedure
a. Isolation of chitin
Crab shells are cleaned by washing and scraping under running water, and
dried in an oven at 100°C. Dry shells (100 g) are broken into fairly large
fragments, and portions containing the eyes are discarded. The fragments are
then decalcified by digestion overnight with 1.5 liter 2N hydrochloric acid at
room temperature. To speed up decalcification, the shells can be ground to a
fine powder, but care must be taken to add the acid slowly to avoid loss of
material due to excessive frothing. The rubbery residues are thoroughly
washed with water and dried at 100°C. The yield of crude chitin is 3 5 - 4 0 g.
b. D-Glucosamine hydrochloride
Concentrated hydrochloric acid (400 ml) is added to the dried residues, and
the mixture is heated on a boiling water bath with continuous mechanical
agitation. After 2.5 hr, by which time dissolution should be essentially com-
plete, an equal volume of water is added, and the solution is separated from
the black sludge by filtration through a bed of a filter aid such as Celite. The
brown filtrate is stirred for 30 min at 60°C with activated carbon, and the
solution is again filtered through Celite. The filtrate should now have a pale
yellow color. The solution is then concentrated at 50 to 60°C under reduced
pressure to a volume of 75 ml. During this process some crystals separate.
Ethanol (4 volumes) is added to the concentrate, and the mixture is stored for
24 hr at room temperature. The product is removed by filtration, washed
successively with ethanol and ether, and air-dried; yield, about 20 g. Purifica-
tion is effected by dissolving the product in a minimal volume of hot water and
adding 4 volumes of ethanol. D-Glucosamine hydrochloride crystallizes as the
α-anomer. Appreciable amounts of the ß-isomer remain in the solution and
may be recovered by precipitation with ether.
References
1. Ledderhose, G. (1876). Ber. 9, 1200.
2. Breuer, R . (1898). Ber. 3 1 , 2193.
3. Westphal, O., and Holzmann, H. (1942). Ber. 75, 1274.
4. Stacey, M., and Webber, J . M. (1962). Methods Carbo. Chem., 1, 228.
Recommended Reviews
1. Foster, A . B . , and Webber, J . M. (1960). Chitin. In "Advances in Carbohydrate Chemistry,"
(M. L. Wolfrom, and R . S. Tipson, eds.), Vol. 15, p. 371. Academic Press, New York.
2. Tracey, M. V . (1955). Chitin, In "Modern Methods of Plant Analysis(K. Paech, and
M. V . Tracey, eds.), Vol. 2, p. 264. Springer-Verlag, New York.
D. Chromatographic Separation of Sugars on Charcoal

1. Introduction
For many years charcoal has been used industrially for the purification of
sugars. In 1932, Hyashi (1) reported that charcoal stirred in an aqueous
acetone-acetic acid solution of glucose and sucrose completely adsorbed the
sucrose but left the glucose in solution. Tiselius (2) proposed that charcoal
might be employed in chromatography for the separation of glucose from
lactose, and later he separated mixtures of glucose and sucrose, and sucrose
and maltose (3). The method of Tiselius has been used by Claesson (4) and by
Montgomery, Weakley, and Hilbert (5). Recently, the versatility of carbon as
an adsorbent for the segregation of sugars into molecular-weight groups was
demonstrated by Whistler and Durso (6). Later, charcoal was used by Whist-
ler and Tu (7) for the separation of sugars from partially hydrolyzed xylan,
and by Whistler and Hickson (8) for the isolation of various sugars from
hydrolytic products of starch. Tu and Ward (9) have improved separation of
disaccharides on heated charcoal columns. Other adsorbents used for car-
bohydrate fractionation include cellulose powder, alumina, silicates, and
ion-exchange resins.
2. Principle
The method described below is according to Whistler and Durso (6).
3. Apparatus
Columns for chromatography
Polarimeter
4. Materials
Celite Maltose Sodium chloride
Charcoal Melibiose Sucrose
Ethanol Sodium bicarbonate Xylose
Glucose
5. Time
4 - 5 hours
6. Procedure
The adsorbent is a mixture of equal parts by weight of Darco-G-60 and Celite,
which has been washed with water and dried. This material is packed into a
glass chromatographic tube measuring 230 x 34 mm, forming a column
170 mm in length. Before the addition of the sugar solution, the column is
moistened with 150 ml water. To effect the displacement of the adsorbed
sugar, water and more powerful developers are used in succession. The
effluent is collected in 100-ml fractions. The course of the desorption process
is followed polarimetrically; a 2-dm tube is used to indicate the complete
removal of each component prior to the addition of the succeeding developer.
a. Separation of mixtures and isolation of components

A mixture of 1.0 g each of glucose, maltose, and rafiinose in the form of a
10% solution is adsorbed on a charcoal column, and is resolved by the
successive introduction of 800 ml water, 1.5 1, 5 % ethanol, and 700 ml 1 5 %
ethanol, for displacement of glucose, maltose, and rafiinose, respectively.
Each of these sugars is obtained in crystalline form. One recrystallization
serves to purify the material sufficiently to give the accepted values of melt-
ing point and rotation. The following mixtures are separated in a similar
manner: maltose and rafiinose; sucrose, melibiose, and rafiinose; glucose and
rafiinose. These mixtures are in the form of 1 0 % solutions containing 1 g of
each sugar.
b. Separation of a sugar mixture in the presence of salts

A mixture of 7 g xylose, 0.6 g maltose, 0.4 g rafiinose, 4 g sodium chloride,
and 0.4 g sodium bicarbonate is dissolved in water and made up to 1 liter.
This mixture can be successfully separated in the above-described manner.
The salts are obtained in the water effluent. Polarimetrie data indicate that
the separation is complete.
References
1. Hyashi, J . (1932). / . Biochem. (Japan) 16, 1.
2. Tiselius, A . (1941). Arkiv. Kemi, Mineral Geol. 14B ( 3 2 ) , 8.
3. Tiselius, A . (1943). Kolloid Ζ 105, 101.
4. Claesson, S. (1947). Arkiv. Kemi, Mineral Geol 24A (16), 9.
5. Montgomery, Ε . M., Weakley, F . B . , and Hilbert, G. Ε . (1949). J. Am. Chem. Soc. 7 1 ,
1682.
6. Whistler, R. L . , and Durso, D . F . (1950). J. Am. Chem. Soc. 7 2 „ 677.
7. Whistler, R. L . , and Tu, C.-C. (1952). / . Am. Chem. Soc. 74, 3609.
8. Whistler, R. L . , and Hickson, J . L. (1954). J. Am. Chem. Soc, 76, 1671.
9. Tu, C.-C, and Ward, K. (1955). / . Am. Chem. Soc. 77, 4938.
Recommended Reviews
1. Binkley, W. W. (1955). Column chromatography of sugars and their derivatives. In "Ad-
vances in Carbohydrate Chemistry," (M. L. Wolfrom and R. S. Tipson, eds.), Vol. 10,
p. 55. Academic Press, New York.
E. Gas—Liquid Chromatography of Carbohydrates

1. Introduction
The application of gas chromatography to the separation of carbohydrates
and related polyhydroxy compounds has been restricted owing to the lack of
volatility of these compounds and to the difficulties involved in the prepara-
tion of volatile derivatives of carbohydrates.
The first report of the application of gas-liquid partition chromatogra-
phy to carbohydrates (1) described the separation of tri-O-methyl derivatives
of methyl pentapyranosides from tetra-O-methyl derivatives of methyl hexa-
pyranosides. The separation of polyacetyl derivatives of carbohydrates was
reported by Bishop and Copper (2). Kircher (3) described the separation of
fully methylated anomeric methyl glycopyranosides.
More recently, acetyl derivatives were used for the resolution of amino
sugars and for the separation of acetal and ketal derivatives (4). Hedgley and
Overend (5) and Ferrier (6) have described the preparation and analysis of
carbohydrates in the form of the remarkably volatile trimethylsilyl ethers.
2. Principle
The method described below (7) involves the solution or suspension of
carbohydrates in pyridine, followed by reaction with hexamethyldisilazane
(CH3) 3SiNHSi(CH 3)3 and trimethylchlorosilane (CH 3) 3SiCl. The resulting
trimethylsilyl ethers ROSi ( C H 3 ) 3 of aldoses, oligosaccharides, and glycosides
(a- and β-isomers) are subjected to gas chromatography on Gas Chrom Ρ

impregnated with 3 % S E - 5 2 .
These ethers can be recovered quantitively and unchanged from the
effluent gas stream, thus showing that no anomerization, hydrolysis, or de-
gradation occurs during the separation.
3. Apparatus
Gas Chromatograph
Stainless steel columns
Microsyringe
4. Materials
Gas Chrom Ρ Pyridine, dry
Glycosides (see procedure) Sugars (see procedure)
Hexamethyldisilazane Trimethylchlorosilane
Oligosaccharides (see procedure)
5. Time
2 - 3 hours
6. Procedure
a. Trimethylsilylation of carbohydrates
Ten mg carbohydrate is treated with 1 ml anhydrous pyridine, 0.2 ml
hexamethyldisilazane, and 0.1 ml trimethylchlorosilane. The reaction is car-
ried out in a 1-dram, plastic-stoppered vial or similar container. The mixture
is shaken vigorously for about 30 sec and allowed to stand for 5 min at room
temperature before chromatography. The solutions become cloudy on addi-
tion of trimethylchlorosilane, but this ammonium chloride precipitate does
not interfere with the subsequent gas chromatography. If the carbohydrate
appears to remain persistently insoluble in the mixture, the vial is warmed
for 2 to 3 minutes at 75 to 85°C.
In some cases where no rearrangements are likely to occur, the sugar
is first dissolved by warming with pyridine, before the addition of hexa-
methyldisilazane and trimethylchlorosilane. From 0.1 to 0.5 μ\ of the result-
ing reaction mixture is used for injection into the gas Chromatograph.
An instrument with hydrogen flame ionization detector is used. The
columns are of stainless steel, 6 ft in length and 0.25 inches in diameter,
packed with Gas Chrom Ρ impregnated with 3 % S E - 5 2 .
b. Operating conditions
In general, flow rates are adjusted for optimal column efficiencies and range
from 75 to 150 ml per min, with inlet pressures of 15 to 20 psi.
The retention times are listed in the following tables.
3
Retention Times of A l d o s e s
Aldose Relative Retention Time at 140°C
/3-Arabinose 0.28
Ribose 0.32
α-Xylose 0.43
/3-Allose 0.81
a-Galactose 0.88
α-Glucose 1.00
/3-Glucose 1.57
α-Gulose 0.75
ß-Mannose 1.08
α-Talose 0.86
"The retention times are relative to that of a-glucose,

which is 20 to 22 minutes at 140°C.
0
Retention Times of Oligosaccharides
Oligosaccharide Relative Retention Time at 210°C
Sucrose 10.4
Lactose 10.5
jS-Maltose 13.1
/3-Cellobiose 16.6
Gentiobiose 22.6
Raffinose 99.0
"The retention times are relative to that of α-glucose,

which is 1.1 to 1.3 minutes at 210°C.
Retention Times of Glycosides*
Glycoside Relative Retention Time at 140°C
Methyl ß-arabinoside 0.20

Methyl a-arabinoside 0.21
Methyl a-xyloside 0.31
Methyl /3-xyloside 0.34
Methyl a-mannoside 0.59
Methyl jS-mannoside 0.67
Methyl a-glucoside 0.92
Methyl /3-glucoside 1.07
fl
The retention times are relative to that of α-glucose (see
aldoses).
References
1. Mclnnes, A . G . , Ball, D . H., Cooper, F . P., and Bishop, C. T. (1958). J. Chromatogr. 1, 556.
2. Bishop, C. T . , and Cooper, F . P., (1960). Can. J. Chem. 38, 388.
3. Kircher, H. W. (1960). Anal. Chem. 32,1103.
4. Jones, H. G . , Jones, J . Κ. N., and Perry, M. B . (1962). Can. J. Chem. 40, 1559.
5. Hedgley, E . J . , and Overend, W. G. (1960). Chem. Ind. (London) 378.
6. Ferrier, R . J . (1962). Tetrahedron 18, 1149.
7. Sweeley, C. C , Bentley, R . , Makita, M., and Wells, W. W. (1963). J. Am. Chem. Soc. 85,
2497.
Recommended Reviews
1. Bishop, C. T . (1962). Separation of carbohydrate derivatives by gas-liquid partition chroma-
tography. In "Methods of Biochemical Analysis(D. Glick, ed.), Vol. 10, p. 1. Interscience,
New York.
2. Berry, J . W. (1966). Gas chromatography of carbohydrates. Adv. Chromatogr. 2, 171.
F. Thin-Layer Chromatography of Carbohydrates

1. Introduction
Several adsorbents have been used for thin-layer chromatography of carbo-
hydrates. Stahl and Kaltenback (1) employed kieselgur impregnated with
sodium acetate. The ability of borate ions to form complexes with polyhy-
droxy compounds was utilized by Pastuska (2) and Prey (3) for the separation
of various sugars on plates impregnated with boric acid.
Schweiger (4) and Vomhof and Tucker (5) analyzed sugars on cellulose
layers. Prey and coworkers (6) used a mixture of silica gel and kieselgur, 1:4.
Wolfrom and his coworkers (7) have recently used microcrystalline cellulose
for sugar analysis.
2. Apparatus
Applicator for T L C Glass plates, 20 χ 20 cm
Drying oven Spray gun
3. Materials
Acetic acid Glucose Sucrose
Anisaldehyde Naphthoresorcinol Silica gel G
ft-Butanol Phosphoric acid Sulfuric acid
Ethanol Rhamnose Xylose
Ether
4. Time
Preparation of thin-layer plates: 1-2 hours
Development and detection: 3 - 4 hours
5. Procedure
a. Preparation of silica gel G plates
The suspension for five plates (20 x 20 cm) is prepared by shaking 30 g silica
gel G and 60 ml water for 30 sec, and is then spread on the plates with an
applicator to a thickness of 0.25 mm. The plates are then activated at 120°C
for 1 hr.
b. Development
The samples of carbohydrates are dissolved in water and spotted by means of
micropipettes along a line 2 cm above the rim of the plate. Development is
accomplished in rc-butanol-acetic acid-ethyl ether-water, 9 : 6 : 3 : 1 .
c. Detection
Naphthoresorcinol reagent
Spraying with a solution of 0.2% naphthoresorcinol in butanol and 10%
phosphoric acid, followed by heating for 10 min at 100°C, gives a pink color
with ketoses, a green color with aldopentoses, and a blue color with aldo-
hexoses.
Anisaldehyde reagent
This reagent is prepared from 0.5 ml anisaldehyde in 9 ml ethanol ( 9 5 % ) ,
0.5 ml concentrated sulfuric acid, and 0.1 ml acetic acid.
Detection of Sugars
Sugar Rf Color with Anisaldehyde
Sucrose 0.09 Violet

Glucose 0.22 Blue
Fructose 0.27 Violet
Xylose 0.40 Gray
Ribose 0.47 Blue
Rhamnose 0.55 Green
References
1. Stahl, Ε . , and Kaltenbach, U. (1961). J. Chromatogr. 5, 351.

2. Pastuska, G. (1961). Z. Anal. Chem. 179, 427.
3. Prey, V . , Verbalk, H., and Kausz, M. (1962). Mikrochim. Acta 449.
4. Schweiger, A . (1962). / . Chromatogr. 9, 374.
5. Vomhof, D . W., and Tucker, T . C. (1965). J. Chromatogr. 17, 300.
6. Prey, V . , Scherz, V . , and Bancher, E . (1963). Mikrochim. Acta 3, 567.
7. Wolfrom, M. L . , Patin, D . L . , and de Lederkremer, R . M. (1965). / . Chromatogr. 17, 488.
Recommended Reviews
1. Fried, B . , and Sherma, J . (1982). Thin-layer chromatography of carbohydrates. In "Thin-
Layer Chromatography," p. 246. Marcel Dekker, New York.
2. Stahl, Ε . , and Kaltenbach, U. (1965). Sugars and derivatives. In Stahl, Ε . "Thin-layer
Chromatography," p. 461. Academic Press, New York.
G. Separation of Carbohydrates by High-Performance Thin-Layer

Chromatography
1. Introduction
In view of the increased concern about nutrition and food labeling for a wide
variety of foods and food ingredients, particularly in regard to their sugar
content, a fast analytical method was needed. The separation of mono-, di-
and trisaccharides on thin-layer chromatoplates was very popular, even
though it is time consuming. A rapid and efficient separation of carbohyd-
rates at ambient temperatures has been achieved on HPTLC ready-to-use
Si 50.000 plates.
2. Apparatus
Developing chamber.
3. Materials
Acetone Diphenylamine
Aniline Si 50.000 HPTLC plates.
4. Time
1 hour
5. Procedure
The HPTLC ready-to-use plate Si 50.000 is first precleaned by developing it
with a mixture of chloroform and methanol 1:1 (v/v) and allowing the
solvent to run to the top of the plate. The plate is then reactivated by drying
for 30 min at 110°C. The mixture of mono-, di- and trisaccharides (raffinose,
lactose, sucrose, glucose, and fructose) (100mg/ml) is now applied to the
plate with a glass capillary.
Ascending one-dimensional double chromatography at room tem-
perature is accomplished with the developing solvent acetonitrile-water,
17:3 (v/v).
After drying in a hood at room temperature the plate is sprayed
with a chromogenic solution prepared by dissolving aniline (2 ml) and
diphenylamine (2 g) in acetone (80 ml), then cautiously adding phosphoric

acid ( 8 5 % , 15 ml) and adding acetone to give 100 ml solution.
Heating the plate at 105-110°C for 15 min reveals fructose as a greyish
red spot, glucose and lactose as a greyish blue spot, and rafiinose and sucrose
as a grey spot. By exposing the plate to ammonia fumes for 15 min, all
carbohydrates appear as ocher yellow spots on a colorless background.
Recommended Reviews
1. Bragg, R . W., Chow, Y . , Dennis, L . , Ferguson, L. N., Howell, S., Morga, G . , Ogino, G . ,
Pugh H., and Winters, M. (1978). Sweet organic chemistry. J. Chem. Ed. 55, 2 8 1 - 2 8 5 .
2. Creammer, B . , and Ikan, R . (1977). Properties and syntheses of sweetening agents. Chem.
Soc. Revs. 6, 4 3 1 - 4 6 5 .
3. Davidson E . A. (1967). "Carbohydrate Chemistry." Holt, Rinehart & Winston, New York.
4. Guthrie, R . D . , and Honeyman, J . (1964). "An Introduction to the Chemistry of Carbohy-
drates." Clarendon Press, Oxford, England.
5. Pigman, W. (1957). "The Carbohydrates." Academic Press, New York.
6. Van Dyke, S. F . (1960). "The Carbohydrates." Interscience, New York.
H. Questions
1. Distinguish between each of the following pairs of terms: (a) aldose

and ketose; (b) D and L in sugar classification; (c) epimer and
enantiomorph.
2. Outline the Kiliani synthesis of sugars and the Ruff method for
degrading sugars.
3. Show how D-glucose reacts with reducing agents; with oxidizing
agents; with cupric sulfate; with Phenylhydrazine.
4. Why are aldohexoses less reactive than aliphatic aldehydes?
5. Draw the two chair conformations for the a- and ß-anomers of the
pyranose form of each of the following D-aldohexoses: mannose,
glucose, galactose, and talose.
6. Name four disaccharides made up of glucose units only and explain
how they differ from each other.
7. What are the chief carbohydrates in honey, fruit, liver, blood, milk,
and cereals?
8. Discuss the occurrence of pentose-yielding substances in nature. What
commercial value do they have?
9. Trehalose, a nonreducing disaccharide, is found in insects.
Methylation and hydrolysis of this compound yield two moles of
2,3,4,6-tetra-O-methyl-D-glucopyranose from each mole of trehalose.
If both anomeric carbon atoms have an α-configuration, what is the
structure of trehalose?
10. Describe in detail the photosynthesis of glucose.
II. Polysaccharides 93
I. Recommended Books
1. Balazs, Ε . Α . , and Jeanloz, R . W. (eds.) (1965). "The Amino Sugars"

2. Bollenback, G. N. (1958). "Methyl Glycosides." Academic Press,
New York.
3. Calvin, M., and Bassham, J . A. (1962). "The Photosynthesis of
Carbon Compounds." Benjamin, New York.
II. POLYSACCHARIDES
A. Introduction
Polysaccharides are polymers of monosaccharides. They are found in the

higher plants, in ferns and mosses, in seaweed, in fungi, in bacteria, and in
animals, where they serve as a structural support and as food reserves. Many
of the polysaccharides are hydrolyzed by specific glycosidases. Thus, cellulose
is hydrolyzed by cellulase, and the starches and glycogens by the amylases
and diastases. On complete acid hydrolysis, the following monosaccharides
are formed: D-glucose, D-mannose, D-fructose, D-galactose, D-xylose, L - and
D-arabinose, D-glucosamine, D-galactosamine, and D-glucuronic acid.
1. Cellulose
Cellulose is the chief constituent of the fibrous parts of plants, and is used for
the preparation of paper, rayon, explosives, and plastics. X-ray analysis of
cellulose fibers indicates that they are arranged in a bundle called a micelle.
The molecular weight of cellulose from different sources may range from
100,000 to 2,000,000. Cellulose consists of D-glucopyranose units linked
through Q and C 4 . The chain is linear and is composed of 100-200 units.
C H 2O H C H 2O H
0
\T°"Vo"
ΟΗ
Η, ΟΗ
H
HO ψΗ Η^
C H 2O H H ΟΗ C H 2O H
Jn
Cellulose chain
Polysaccharides extractable from the cell walls by dilute aqueous alkali

are called hemicelluloses. The most abundant hemicellulose polysaccharides
are the xylans, which are composed of D-xylose units. Some xylans are linear,
while others have a branched structure. Xylans occur mainly in corncobs,

corn stalks, grain hulls, and stems.
A xylan from corncobs consists of a linear chain of D-xylopyranose units
connected by /3-D-I—»4 bonds:
OH H OH
-0 -O -Q i-Ofi
OH 'OH
H.OH
,OH \OH
HO -O
H
-o- 1
OH
OH
Xylan
Its molecular weight is about 30,000.
The red seaweed, Rhodymenia palmata, contains a xylan composed of
D-xylopyranose units and has 1 —» 3 and 1 —* 4 linkages in the ratio of about
1:3.
Mannans are also hemicelluloses. They probably consist of a chain of
D-mannose units linked 1—»4, with side chains of D-galactopyranose linked
l-»6.
2. Starch
Starches are mixtures of two polysaccharides, amylose and amylopectin.

Amylose constitutes about 2 0 % and is made up of approximately 300 D -
glucose units linked by 1—»4 a-glucosidic bonds, which form a helix with
about six glucose residues per turn. In the presence of diastase, it is hydro-
lyzed completely to maltose; acidic hydrolysis yields D-glucose quantitatively.
CH,OH CH,OH CH,OH

H
Η
νΟΗ Η/
O ^ •—Ο-
Η ΟΗ
η
Amylose
Amylopectin is the major constituent of starch. Its hydrolysis with

distase gives a 5 5 % yield of maltose, the remainder being a dextrin. Complete
acid hydrolysis yields D-glucose only. In amylopectin the majority of units are
linked by α-D-l—>4 and α-D-l—>6 glucosidic bonds at the branch points.
Many reagents, such as chloral hydrate, thymol, nitropropane, and
H-butanol, have been used for the separation of amylose from amylopectin.
CH,OH
1 1,6-linkage
-O—
OH H HO
C H 2O H
HO -O
OH OH
Î
1,4-linkage
Amylopectin
3. Glycogens
Glycogens are reserve carbohydrates of animals and are stored in the liver
and muscles. They have highly branched chains; on enzymatic degradation
they form maltose and a dextrin. Glycogens yield D-glucose on complete
acidic hydrolysis.
4. Fructans
Fructans are D-fructose polymers that occur in the roots, stems, and seeds of
various plants. They are subdivided into the following two types: those with a
l,2'-linkage, and those with a 2,6'-linkage.
5. Inulin
Inulin occurs in the tubers of chicory, in the Jerusalem artichoke, and in the
bulbs of onion and garlic. Complete hydrolysis gives D-fructose and some
OH
CH.OH
Inulin
D-glucose. The chain of inulin consists of about 35 D-fructofuranose residues

linked ß-1—»2. Inulin serves as a source of commercial fructose.
6. Levari
Levan is a gummy product of the attack of certain organisms on solutions of
sucrose and raffinose. Levan gives a very high yield of crystalline fructose on
hydrolysis.
7. Dextrans
Dextrans are produced in processes such as the manufacture of sugar from

beets and wine-making, and from sucrose by the agency of bacteria such as
Leuconostoc dextranicum.
8. Plant Gums
When a plant suffers injury by insect, bacterial, or fungal attack, it often

exudes a viscous, sticky fluid that tends to seal the wounds. These exudates
are mostly polysaccharides and are usually highly branched.
Gum arabic is one of the most important gums and is used in confec-
tionery and medicaments. On complete hydrolysis, it yields L-arabinose,
L-rhamnose, D-galactose, and D-glucuronic acid.
9. Pectins
Pectins are widespread in nature and are found in the pulp of citrus fruits,
carrots, apples, beets, etc. They are widely used for the gelation of fruit
juices. Pectin is the methyl ester of pectic acid and is composed of long chains
of galacturonic units.
OH COOCH 3 OH
Pectin
10. Chitin
Chitin is a polyglucosamine that occurs mainly in invertebrates. It forms the
exoskeletons of crustaceans and insects. Complete acid hydrolysis of chitin
gives very high yields of D-glucosamine and acetic acid, whereas controlled
acid or enzyme hydrolysis produces N-acetyl-D-glucosamine.
C H 2O H NHAc C H 2O H NHAc
Ο rOn Ο -On
x
OH OH
OH OH
Ο L
NHAc CH,OH
L
o J
NHAc CH,OH
0
Chitin
11. Heparin
Heparin is a blood anticoagulant that is found in the liver, lungs, thymus,
spleen, and blood. It is a polymer of D-glucuronic acid and D-glucosamine.
The amino group and some of the hydroxyls are sulfated. The molecular
weight of heparin appears to be about 17,000 to 20,000.
CH,OH COOH C H 2O H COOH
vOH
B a / 2 0 S 0 20 O- -O- L-O
OH H N S 0 2O B a / 2 O S 0 2B a / 2 .
H N S 0 2O B a / 2
B a / 2 0 S 0 20
Heparin
B. Isolation of Amylopectin and Amylose from Potato Starch
1. Introduction
Many different methods have been used to fractionate starch into its branched
and linear components. The method most suitable for one kind of starch is
not necessarily the best for another, and much depends upon the source and
pretreatment of the starch. In 1941, Schoch (1) demonstrated that slow
cooling of a hot, aqueous starch solution saturated with butanol gives a
microcrystalline precipitate of the linear starch component, amylose. Frac-
tionation of starch by leaching techniques was applied by Baum and Gilbert
(2), who utilized the insolubility in cold, dilute alkali of the amylopectin
fraction from undamaged starch granules. Using the same freshly prepared
starch and working under anaerobic conditions, these authors found that
heating of starch suspensions in distilled water for 5 min at 100°C yields the
amylose fraction. Another method calls for the use of chloral hydrate, which
forms a complex with amylose, amylopectin remaining in the mother liquor.
Fractionation by fractional precipitation is achieved by addition of salts (e.g.,
M g S 0 4 ) or alcohols (e.g., ethanol and methanol).
C H 2O H CH,OH C H 2O H
,ΟΗ
HCT 4o-
OH
Amylose
CH,OH CH,OH
HO
CH,OH
vOH
oJ -o-
OH OH OH
Amylopectin
2. Principle
In the following method (3) starch is separated into its principal components-
amylose and amylopectin—by addition of dilute alkali followed by neutral-
ization. Amylose remains in solution, while amylopectin forms a gel. The
former is precipitated selectively from the saline solution by addition of
n-butanol; removal of the butanol from the amylose-butanol complex yields
pure amylose. Amylopectin is isolated by centrifugation followed by freeze-
drying.
3. Apparatus
Blender
Centrifuge
Stirrer
4. Materials
Butanol Sodium chloride
Hydrochloric acid Sodium hydroxide
Potatoes
5. Time
Settling of a gel: overnight
Isolation: 5 - 6 hours.
6. Procedure
a. Preparation of potato starch
One kg undamaged potatoes is peeled, sliced, and then extracted in 250-g
lots with 750 ml 1% sodium chloride solution in a mechanical food blender.
Each lot is blended for about half a min, and the slurry is then filtered
through fine muslin with gentle agitation. The filter cakes are bulked and
reextracted for one min with 150 ml salt solution. The slurry is filtered
through the muslin as before, and the filtrates are bulked. The starch gran-
ules are allowed to settle, and the supernatant, together with fragments of
cellulose that have passed through the muslin, is decanted and discarded.
The starch is washed three times with 1% sodium chloride and then once
with 0.017V sodium hydroxide. The solution is finally washed three times
with distilled water and stored underwater at 4°C. Precautions must be
taken against freezing, as this would alter the starch; yield, about 40 g wet
starch. Before samples of the starch are weighed, the supernatant is poured
off, and the solid is drained for a moment; the dry weight is approximately
5 0 % the weight of the drained solid.
b. Dispersion of the starch

To 3.3 liters 0.1577V sodium hydroxide in a glass-walled tank is added 40 g
drained, freshly prepared starch, weighed wet and suspended by gentle shak-
ing in 260 ml water. The temperature of the dispersion must be at least 22°C,
but should preferably be near 25°C. The mixture should be stirred gently until
it clears. The method of stirring is of vital importance; motor-driven stirrers
or the bubbling of gas through the mixture must not be used, since the gel
structure of the amylopectin is damaged thereby, and this makes subsequent
separation difficult. Gentle stirring with a plate-glass strip is sufficient. The
alkaline solution should stand for a total of 5 min; 915 ml 5 % sodium chloride
solution is added, and the dispersion is neutralized with I N hydrochloric acid
to pH 6.5-7.5 with the aid of an external indicator or long-lead glass electrode
assembly.
After standing overnight at room temperature, the gel settles until it
occupies about one third of the total volume. There should be a sharp division
between the gel and the amylose solution; the latter is then removed by
siphoning or by suction, and should be filtered through a 15-cm fritted-glass
filter (No. 3 ) . This solution is then filtered through a No. 4 filter.
c. Precipitation of amylose
The amylose retrogrades if stored as a saline solution for more than a few
days. It should thus be separated from this solution as soon as possible.
Butanol is used to precipitate the amylose selectively from the saline solution
according to the following procedure. The filtrate is saturated with redistilled
butanol and stirred gently with a motor-driven stirrer for about 1 hr at room
temperature. The precipitated amylose-butanol complex is allowed to set-
tle for 2 to 3 hrs, and the clear supernatant is siphoned off. The partially
sedimented solid is then centrifuged at 3000 rpm for 15 min in polypropylene
buckets. The complex is then stirred in butanol-saturated water (125 ml) and
reconcentrated by centrifuging as before. With some samples of starch, a
further precipitation may be necessary. The complex is stable if stored in a
stoppered container. It is readily soluble in water at room temperature. To
remove most of the butanol from this solution, oxygen-free nitrogen is bub-
bled through it for 10 min in a vessel heated in a boiling water bath; 40 g wet
potato starch yields 1.5-1.8 g amylose.
d. Purification of amylopectin
The amylopectin gel is centrifuged at 8000 rpm for 20 min at 20°C. The
supernatant is discarded, and 1% sodium chloride solution is added to the gel
(100 ml per 4 g original wet starch) with stirring. The mixture is allowed to
stand for 20 hr at 18°C, and the gel is then collected by centrifuging at
8000 rpm as before. A second washing with sodium chloride is necessary.
After centrifuging, the gel can be either suspended in water for immediate use
(it is insoluble in cold water) or freeze-dried and stored; 40 g wet starch yields
approximately 6 g amylopectin.
e. Iodine test
A few granules of the polysaccharide in 1 ml water are treated with sev-
eral drops of a dilute solution of iodine in potassium iodide (prepared by
dissolving 1.8 g potassium iodide in 15 ml water and then adding 1.2 g
iodine). Starch gives an intense blue color; amylose exhibits a blue color; and
Amylopectin develops a reddish color.
References
1. Schoch, T. J . (1941). Cereal Chem. 18, 121.
2. Baum, H., and Gilbert, G . (1956). / . Colloid Sei. 11, 428.
3. Gilbert, L. M . , Gilbert, G . Α . , and Spragg, S. P. (1964). Methods of Carbo. Chem.
4, 25.
Recommended Reviews
1. Muetgeert, J . (1961). The fractionation of starch. In "Advances in Carbohydrate Chemistry"
Wolfrom, M. L. and Tipson, R . S. (eds.), Vol. 16, p. 299. Academic Press, New York.
2. Schoch, T. J . (1945). The fractionation of starch. In "Advances in Carbohydrate Chemistry
W. W. Pigman, and M. L. Wolfrom, (eds.), Vol. 1, p. 247. Academic Press, New York.
C. Isolation of Wood Cellulose
1. Introduction
Cellulose, as a naturally occurring fiber, is widespread in nature, mainly in
woody tissues. However, it has also been found in some lower animals, in
bacteria, and in certain mammalian muscle tissues.
In 1868, Fremy aand Terreil (1) treated wood with chlorine and then
with aqueous potassium hydroxide to obtain a crude cellulose. This work was
followed by that of Cross and Bevan (2), who also used chlorination as the
first step, but then extracted the chlorinated lignin with hot aqueous sodium
sulfite solution. Many other methods of delignifying wood and plants were
subsequently developed; two of these are the Van Beckum and Ritter method
(3) and the Jame-Wise method ( 4 , 5 ) . These methods are aimed at retaining
the maximal amout of carbohydrate in the resulting "holocellulose," whereas
the Cross and Bevan method is not.
Cellulose invariably undergoes degradation during delignification, and
it thus appears to be impossible to isolate a wood cellulose showing the same
degree of polymerization as that in the original wood or plant. The two major
components to be removed are xylan and mannan; other polysaccharides,
such as galactan, araban, and glycuronans, are easily removed. Softwoods
contain large amounts of mannan and some xylan, and the resulting wood
cellulose may retain appreciable amounts of mannan.
CHoOH C H 2O H Η OH
^ - o r-O
OH >H,OH
,H
HO
OH CH,OH Η OH CHjOH
Jn
Cellulose chain
2. Principle
Delignification of wood is performed by treating wood meal with a solution of
sodium chlorite at about 70°C [6]. These pH and temperature conditions are
the most suitable for the removal of xylan and mannan, since the lower
temperatures the rate of delignification is slower. The resulting holocellulose
is then extracted with alkali to remove certain soluble carbohydrates, e.g.,
hemicelluloses or a- and /3-celluloses, and α-cellulose or alkali-resistant cellu-
lose is left as a residue. More thorough extraction will remove most of the
nonglucan polysaccharides and leave an essentially pure wood cellulose.
3. Apparatus
Screw cap bottle
4. Materials
Acetic acid Sodium chlorite

Benzene Sodium hydroxide
Ether Wood meal
5. Time
Chloriting treatment: 4 hours

Alkaline extraction: 24 hours
6. Procedure
a. Preliminary treatment
Samples of wood meal 25 g are used as the starting material. The wood meal
should preferably be of 40 to 60 mesh; a finer particle size is to be avoided.
It can be prepared from coarse sawdust, wood chips, or thin spokeshave
shavings.
In the case of conifer wood, the meal is extracted with 2:1 benzene-
ethanol and then with 9 5 % ethanol, or else with 9 5 % ethanol and then with
ether. This extraction is not necessary when dealing with most nonresinous
woods.
b. Chloriting treatment
The air-dried sample is suspended in 800 ml hot water in a 2-liter Erlenmeyer
flask also containing 3 ml glacial acetic acid. Technical-grade sodium chlorite,
7.5 g, is then added. This addition of sodium chlorite and subsequent opera-
tions, including washing, should be carried out in a well-ventilated hood. The
flask is stoppered with an inverted 50-ml Erlenmeyer flask and heated on a
steam bath. The period of heating is generally 3 0 - 6 0 min; the temperature of
the solution will be about 70°C.
Depending on the type of wood used, this operation may have to be re-
peated several times. For samples of temperate hardwood, a total of 3 steps,
or a total reaction time of 3 hr is generally sufficient. Tropical hardwoods will

require more steps. In the case of softwood, heating periods of up to 6 hr may
be necessary. The final residue should be almost white and retain the woody
structure of the original sample. In some cases, the residue will have a slight
yellow color.
c. Washing
When a satisfactory degree of whiteness has been attained, the mixture is
filtered on a Büchner funnel, and the holocellulose is thoroughly washed with
2 liters cold water. The product is air-dried for subsequent alkaline extrac-
tion.
d. Alkaline extraction of holocelluloses of softwood

The sample (20 g air-dry holocellulose) is added to a 1-liter, wide-mouthed,
screwcap bottle, 1 liter of 12% sodium hydroxide solution is added, and a
stream of high-purity nitrogen is bubbled through for 1 min. The bottle is
then securely closed with a polyethylene liner and screwcap, and stirred
gently by rotating end-over-end at 6000 rpm for 24 hr at room temperature.
The mixture is then filtered by suction on a fritted-glass Büchner funnel (C
porosity) with the aid of a rubber dental dam. No attempt is made to exclude
air during this Alteration, but a minimal amount of air is sucked through the
filter. The volume of filtrate is noted in order to determine the volume of
alkali retained in the holocellulose on the filter.
The first extract will generally be brown in color because of the lignin
present. Later extracts will be lighter in color, and finally colorless.
The residue is returned to the bottle, and 1 liter of 7 . 1 % sodium
hydroxide is added in three portions. In this manner, three extractions are
made with the sodium hydroxide over a period of 24 hr. After the final
extraction, the mixture is filtered, and the residue is washed with 5% sodium
hydroxide and then with cold water. It is then stirred briefly in the funnel with
10% acetic acid and allowed to stand for 10 min. The mixture is filtered, and
the wood cellulose is washed thoroughly with water. The wood cellulose is
air-dried and analyzed for sugar constituents by a suitable method.
References
1. Fremy, E . and Terreil, A . (1868). Bull. Soc. Chim. France. 9, 437.
2. Cross, C. F . , Bevan, E . J . , and Beadle, C. (1895). "Cellulose and Outline of the Chemistry
of the Structural Elements of Plants," p. 95. Longmans, Green and C o . , London, England.
3. Van Beckum, W. G . , and Ritter, G. J . (1937). Paper Trade J . 105 (18), 127.
4. Jame, G. (1942). Cellulose chemie 20, 43.
5. Wise, L . E . , Murphy, M . , and D'Addieco, A. A. (1946). Paper Trade J . 122 ( 2 ) , 35.
6. Green, J . W. (1963). Methods Carbo. Chem. 3, 9.
Recommended Reviews
1. Hatch, R . S. (1954). Bleaching and purification of wood cellulose. In "Cellulose and Cellulose
Derivatives" Ott, E , Spurlin, Η. M., and Grafflin, M. W. (eds.), Vol. 2, p. 589. Intersci-
ence, New York.
2. Polglase, W. J . (1955). Polysaccharides associated with wood cellulose. In "Advances in
Carbohydrate Chemistry" Wolfrom, M. L. and R . S. Tipson, (eds.), Vol. 10, p. 283.
Academic Press, New Y o r k .
D. Questions
1. Compare starch and cellulose from each of the following aspects:

source, intermediate and final hydrolysis products, structure of the
polymer chain, their function in nature.
2. Define and give the structural formulas of the following compounds:
lignin, pentosans, glycogen, collodion, gum cotton, dextrin.
3. What is pectin? Give the formulas of its hydrolytic products. Of what
commercial value is pectin?
4. Write the structural formula of chitin. Where it is found in nature?
5. Compare the physical properties of mono- and polysaccharides.
6. Where are starches most commonly found? What is a soluble starch?
7. How does a plant synthesize starch? What is the difference between
amylose and amylopectin?
E. Recommended Books
1. Brautlecht, C. A. (1953). "Starch, Its Sources, Production, and Uses."

Reinhold, New York.
2. Honeyman, J . (1959). "Recent Advances in the Chemistry of Cellulose
and Starch." Heywood and Co.
3. Sjöstrom, Ε . (1981). "Wood Chemistry, Fundamentals and
Application." Academic Press, New York.
4. Thiem, J . , (ed.) 1990. "Carbohydrate Chemistry. Topics in Current
Chemistry " Vol. 154. Springer-Verlag, New York.
5. Van Dyke, S. F. (1960). "The Carbohydrates." Interscience, New
York.
6. Whistler, R . L . , and Smart, C. L. (1953). "Polysaccharide Chemistry."
ISOPRENOIDS
I. CAROTENOIDS
A. Introduction
The carotenoids are yellow, orange, or red pigments, which are widely
distributed in the plant and animal kingdoms. They are called lipochromic
pigments because they are soluble in fats. In the animal organism the
carotenoids are either dissolved in fats or combined with protein in the
aqueous phase. In the higher plants the carotenoids are found in the leaves
together with chlorophyll; they also constitute the principal pigments of
certain yellow, orange, and red flowers and of many microorganisms.
The carotenoids comprise two groups: hydrocarbons, soluble in pe-
troleum ether; and xanthophylls, oxygenated derivatives of the carotenes.
These compounds are alcohols, aldehydes, ketones, epoxides, and acids
soluble in ethanol.
1. Hydrocarbons
The three isomeric orange-red carotenes isolated from carrots are α-, β- and
γ-carotene; the red carotenoid hydrocarbon of tomatoes is lycopene.
t-Carotene
105
106 CHAPTER 3 Isoprenoids
y-Carotene
A series of partly saturated carotene hydrocarbons (e.g., phytofluene,

phytoene) has recently been discovered in various plant tissues. These
carotenes appear to be lycopene derivatives.
2. Xanthophylls
Xanthophylls may be classified as follows:
Hydroxylated carotenoids such as cryptoxanthin, lutein, and zeaxan-
thin. The hydroxyl group can exist either free or esterified.
Zeaxanthin
Methoxylated carotenoids such as rhodovibrin. They are lycopene derivatives

substituted at position 1.
Rhodovibrin
I. Carotenoids 107
Oxocarotenoids such as capsanthin and rhodoxanthin.
Rhodoxanthin
Epoxycarotenoids exist in nature as 5,6- and 5,8-epoxides, e.g., violaxanthin

and flavoxanthin. Luteochrome contains both the 5,6- and 5,8-epoxide
systems.
Violaxanthin
Flavoxanthin
Luteochrome
Carboxycarotenoids such as bixin and crocetin.
Crocetin
Almost all naturally occurring carotenoids are tetraterpenoids consist-

ing of eight isoprenoid molecules. On the basis of X-ray and spectral analysis,
it was shown that, with a very few exceptions, the double bonds of the natural
carotenoids have a trans configuration. In most naturally occurring cyclic
carotenoids, the linkage between the terminal ring and the central chain is via
a single bond. However, by dehydrogenation it is possible to transform this
linkage into a double bond. The compounds are then designated by the prefix
retro.
Retrodehydro-ß-carotene
The methods used for elucidating the constitution of carotenoids are

catalytic hydrogénation or addition of halogen, iodine chloride, or oxygen
for determination of double bonds; oxidation with chromic acid of the side-
chain methyls into carboxyl groups; oxidative degradation with potassium
permanganate and ozone.
Chromatography (column, paper, and thin-layer) has proved to be a
powerful and essential tool for the isolation and structural determination of
carotenoids. The synthesis of the polyene pigments involves the union of a
bifunctional unit forming the central part of the molecule with two molecules
that form its terminals.
Combination of units C l 9 + C 2 + C 1 9 .
jß-Carotene, zeaxanthin, and physalien have been prepared in this way.
+ BrMgC^CMgBr • ^-Carotene
I. Carotenoids 109
Combination of units C 1 6 + C 8 + C 1 6 .
In this process, the center of the molecule is an unsaturated diketone
that reacts with two molecules of a C 1 6 acetylene.
jS-Carotene
Combination of units C14 + C12 + C14.

/3-Carotene may be synthesized by a combination of a bis-enol ether
and the acetal of a C 1 4 aldehyde.
jS-Carotene
Numerous investigators in recent years have tried to establish the

significance of carotenoids in plants. Some investigators claim that carotene
and xanthophyll fulfil the role of light filters for chlorophyll, while others
suggest that they function as protectors of enzymes in the cell.
It is noteworthy that while plants and microorganisms synthesize their
carotenoids, those present in the tissues of higher animals are derived from
dietary sources, e.g., ß-carotene, which is converted into vitamin A in the
animal organism. Furthermore, certain carotenoids play a part in the visual
process.
The biosynthesis of carotenoids has been studied much more extensively
than that of any of the other terpenoids. The following is a generalized
scheme.
Isopentenyl pyrophosphate — > Geranyl pyrophosphate

P l i n e n z a t l o n
Farnesyl pyrophosphate Geranylgeranyl pyrophosphate >
Phytoene — > Carotenoids.

The main building unit from which isopentenyl pyrophosphate (IPP) is

synthesized is mevalonate. It has not yet been established whether the various
carotenoids are interconvertible or whether they arise via parallel paths from
a common C 4 0 precursor.
B. Isolation of Capsanthin from Paprika

1. Introduction
The first investigation of paprika pigments was carried out by Braconnot in
1817 (1). In 1927, Zechmeister and von Cholnoky (2) obtained the pigment of
Capsicum annuum (paprika) in a crystalline form and proposed the name
capsanthin.
Capsanthin is a rare carotenoid. It was found in the esterified form in
the ripe pods of Capsicum annuum and Capsicum frutescens japonicum ( 3 , 4 ) .
Karrer and Oswald (5) observed that the anthers of Lilium tigrinum contain
capsanthin.
Capsanthin is well adsorbed on calcium carbonate or zinc carbonate
from solutions of carbon disulfide or from a mixture of benzene and ether.
.OH
Capsanthin
2. Principle
Capsanthin, the main carotenoid of paprika, is first extracted from paprika
pods with petroleum ether at room temperature. Since capsanthin, like most
hydroxylated carotenoids, occurs in nature in the ester form, it is saponified
by means of 3 0 % methanolic potassium hydroxide at room temperature (6).
For further purification, the crude capsanthin is subjected to column chroma-
tography on suitable adsorbents.
3. Materials
Benzene Ether Petroleum ether
Calcium carbonate Methanol Potassium hydroxide
Carbon disulfide Paprika pods Sodium sulfate, anhydrous
I. Carotenoids 111
4. Time
14-15 hours
5. Procedure
The paprika pods are freed from their shells and seeds and dried at 35 to
40°C. Finally ground pod material (100 g) is stirred with 200 ml petroleum
ether (bp 40-60°C) for 4 hr at room temperature and then filtered through a
Büchner funnel; the solid is washed with 25 ml petroleum ether. The red-
colored solution of petroleum ether is diluted with a threefold volume of
ether, 100 ml 3 0 % methanolic potassium hydroxide is added, the mixture is
stirred for 8 hr, and the free phytoxanthins are dissolved in ether. The
ethereal layer is then washed with water, dried over sodium sulfate, and
concentrated to 20 ml under reduced pressure. The ethereal residue is diluted
with 60 ml petroleum ether and allowed to stand in a cool place for 24 hr. The
red capsanthin is filtered off and crystallized from a small amount of carbon
disulfide.
The separation of capsanthin from the accompanying carotenoids, such
as zeaxanthin and capsorubin, is effected by chromatography on calcium car-
bonate or zinc carbonate. Carbon disulfide or a mixture of benzene and
ether ( 1 : 1 ) is employed as a solvent for developing the chromatogram.
Crystallization from carbon disulfide yields carmine red spheres, mp 176°C.
The pigment crystallizes from petroleum ether as needles, and from methanol
as prisms.
Care should be taken when working with carbon disulfide, since it is
highly inflammable.
a. Color reactions
1. On treating a solution of capsanthin in chloroform with concentrated
sulfuric acid, the latter assumes a deep blue coloration.
2. Capsanthin gives a deep blue coloration with antimony trichloride in
chloroform.
b. Capsanthin
OH
1
c. NMR (nuclear magnetic resonance) (400 MHz)
δ Η 0.840[s, 3H, C H 3 (16')],
1.075[s, 6H, Me(16), Me(17)],
1.207[s,3H,Me(17')j.
1.367[s, 3H, M e ( 1 8 ' j ] ,
1.736[s, 3H, Me(18)],
1.957[s, 3H, M e ( 1 9 ' ) ,
1.974[s, 6H, Me(19), Me(20)],
1.989[s, 3H, Me(20')],
2.39[ddd, J = 17.6, ca 1.5, 1H, H a — C ( 4 ) ] ,
2.96[dd, J = 15.5, 9, 1H, Ha - C ( 4 ' ) ] ,
ca. 4.00[br, m, 1H, H a - C ( 3 ) ] ,
4.52[m, 1H, H a - C ( 3 ' ) ] ,
6.13[s, 2H, H — C ( 7 ) , Η—C(8)],
6.16[d, J = 11.6, 1H, Η—C(10)],
6.26[d; J = 11; 1H, Η—C(14)];
6.35[d, J = 11, ca. 1H, H — C ( 1 4 ' ) ] ,
6.36[d,J= 15,1H,H—C(12)],
6.45[d, J = 15,1H, Η — C ( 7 ' ) ] ;
6.52[d,J = 1 5 , 1 H , H — C ( 1 2 ' ) ] ,
6.55[d, J = 11, 1H, H — C ( 1 0 ' ) ] ,
ca 6.6-6.8[m, 4H, H — C ( l l ) , H — C ( l l ' ) , H—C(15); H — C ( 1 5 ' ) ] ,
7.33[d, J = 15, 1H, Η—C(8')]
13
d. C NMR (100, 6MHz)
5 C 12.75[C(19)], 48.61[C(2)], 132.39[C(14)],
12.79[C(20)], 51.06[C(2')], 133.69[C(9')];
12.84[C(19')j, 59.01[C(5')j, 135.24[C(14')];
12.90[C(20')], 65.41[C(3)], 135.93[C(13')],
21.39[C(18')], 70.44[C(3')], 137.46[C(12)],
21.63[C(18)j, 121.04[C(7')], 137.60[C(13)],
25.16[C(17')j, 124.13[C(11')], 137.85[C(6)],
25.95[C(16')j, 125.58[C(11)], 138.51[C(8)j,
28.80[C(16)], 125.93[C(7)], 140.63[C(10')],
30.32[C(17)], 126.30[C(5)j, 141.97[C(12')j,
42.69[C(4)], 129.74[C(15')]; 146.86[C(8')],
44.01[C(l')j, 131.27[C(10)], 202.82[C(6')j.
45.49[C(4')], 131.68[C(15')],
e. Mass spectrum
Capsanthin C 4 o H 5 60 3 Mol. wt. 584.
m/z 584(75%) 127(36%) 105(44%)
478(62%) 109(100%) 91(65%)
429(6%) 106(31%) 83(56%)
145(51%)
I. Carotenoids 113
f. UV spectrum of capsanthin
n z e en
Ama x 486,520 γημ
Capsanthin is a polyene with 9 conjugated C = C double bonds. The appear-
ance of a peak at 520 ιημ (as compared with 504 π\μ for lycopene) is due to
the introduction of a carbonyl group in conjunction with the system of the
C = C double bond. One such carbonyl thus has a more pronounced bath-
ochromic effect than two C = C bonds.
References
1. Braconnot, H. (1817). Ann. Chim. 6, 122, 133.
2. Zechmeister, L . , and von Cholnoky, L. (1927). Ann. 454, 54.
5. Karrer, P., and Oswald, A . (1935). Helv. Chim. Acta 18, 1303.
Recommended Reviews
1. Goodwin, T. W. (1955). Carotenoids. In "Modern Methods of Plant Analysis" (K. Paech and
M. V . Tracey, eds.), Vol. 3, p. 272. Springer-Verlag, Berlin.
2. Goodwin, T. W. (1965). Distribution of Carotenoids. In "Chemistry and Biochemistry of
Plant Pigments" (T. W. Goodwin, ed.), p. 127. Academic Press, New York.
C. Isolation of Lycopene from Tomatoes

1. Introduction
Lycopene was first isolated from Tamus communis by Hartsen in 1873 (1).
Recent investigations employing highly defined chromatographic methods
have shown that the tomato pigment is widely distributed in nature. It has
been prepared from a variety of fruits and berries (2, 3 ) . The first modern
preparation is that of Willstätter and Escher (4), who processed 75 kg tomato
concentrate and obtained 11 g once-recrystallized lycopene.
Porter and Zscheile (5) have described the chromatographic separation
of carotenes from various species and strains of tomatoes on a magnesium
oxide-Super Sel column.
Lycopene
Recently, (6) four dominant tomato paste carotenoids, phytofluene,

/3-carotene, phytoene, and lycopene were identified using high performance
liquid chromatography (HPLC) with UV-VIS photodiode array detection.
Carotenoid Identified (nm) Structure
Phytoene (275 286 297)
Phytofluene (331 348 368)
Beta-carotene (426 448 476)
Zeta-carotene (378 398 424)
Gamma-carotene (435 461 490)
Lycopene (444 471 501)
2. Principle
Tomato paste is dehydrated with methanol, and lycopene is extracted from
the residue with methanol-carbon tetrachloride. The crude product is crystal-
lized twice from benzene by the addition of methanol, giving lycopene of 98
to 9 9 % purity (7).
Further purification is achieved by a chromatographic procedure, using
calcium hydroxide as the adsorbent.
Lycopene in solution undergoes isomerization even at 20°C. Crystalline
lycopene is not isomerized but has a tendency to autoxidation, especially in
light. It should be kept in the dark in evacuated glass tubes.
3. Apparatus
Centrifuge
4. Materials
Benzene Sodium sulfate, anhydrous
Carbon tetrachloride Tomato paste
Methanol
I. Carotenoids 115
5. Time
5 - 6 hours
6. Procedure
Canned tomato paste, 50 g, in a 3-liter-wide-mouthed bottle is dehydrated by
adding 65 ml methanol. The mixture is immediately shaken vigorously to
prevent the formation of hard lumps. A small sample of the suspension is
tested by hand; if it has a glutinous consistency, more methanol is added to
the main portion to avoid the possible clogging of filters. The mixture is
allowed to stand for 1 to 2 hr and is then shaken vigorously. The thick
suspension is filtered on a Büchner funnel (diameter 2 5 - 2 0 cm). The yellow
filtrate is discarded. The dark red cake is returned to the bottle and shaken
with a mixture of 35 ml methanol and 35 ml carbon tetrachloride. The stopper
of the bottle must fit well and should be lifted for a moment after the mixing,
to release any built-up pressure. Brief shaking followed by opening of the
bottle is repeated until no more excess pressure is noticed. The suspension is
shaken for 10 to 15 min and separated by filtration on a large Büchner funnel.
The filtrate consists of a lower, very dark red, carbon tetrachloride phase and
an orange aqueous-methanolic layer. The slightly colored tomato residue is
crushed by hand to form a nearly uniform powder. It is then reextracted with
35 ml of each solvent as described, and the suspension is filtered. The extrac-
tion is now almost complete. The filtrates are combined, the methanol layer is
transferred to a 2-liter separatory funnel, and 1 volume of water is added. A
white emulsion appears in the upper phase. If the emulsion is reddish, it is
stirred with a glass rod until the droplets of carbon tetrachloride join the
lower layer. The phases are separated and the carbon tetrachloride phase is
washed several times with water. The carbon tetrachloride solution is drained
into a 1-liter Erlenmeyer flask and dried over anhydrous sodium sulfate. The
extract is then poured through a folded filter into a 1-liter round-bottomed
flask equipped with a standard taper. The solvent is evaporated with the aid
of a water pump to about 5 ml in a water bath at 60°C. The solution is
transferred to a similar flask of 10 ml capacity using a few ml carbon tetra-
chloride to rinse the larger flask. The solvent is then removed completely in
vacuo, leaving a dark oily residue, which is diluted with a few ml benzene and
evaporated again to remove the carbon tetrachloride completely. The partly
crystalline, dark residue is transferred quantitatively with 1 ml benzene to a
25 ml Erlenmeyer flask. A clear solution is obtained by immersing the flask in
a hot water bath. Boiling methanol is added in portions, using a dropper, to
the benzene solution, with stirring after each addition, until 1 ml methanol
has been introduced. Crystals of crude lycopene begin to appear immediately.
The crystallization is completed by keeping the liquid first at room tempera-
ture and then in ice water. After standing for 1 to 2 hr, the crystals are
collected on a small Büchner funnel and washed with 2 ml boiling methanol.
The lycopene crystals are transferred to a tared 10-ml centrifuge tube,

the last portion being removed from the funnel with small quantities of
boiling benzene. Benzene is added to the centrifuge tube to make up the
volume to 1 ml. The crystals are dissolved by dipping the tube into hot water
and stirring the contents. When a clear solution is obtained, boiling methanol
is introduced in small portions with a dropper, and the solution is stirred with
a glass rod until crystals begin to appear. The centrifuge tube is kept at room
temperature for a short time and then an ice bath. More methanol is added in
small portions, with stirring, to the cold solution. The total volume of metha-
nol present should not exceed 1 ml.
The mixture is allowed to stand for 2 hr in the ice bath, and the crystals
are separated by a brief but strong centrifuging. The mother liquor is de-
canted and discarded. The crystals are treated in the centrifuge tube with 1 ml
boiling methanol. The mixture is stirred and the methanol is removed by
centrifuging before it cools. The methanol is decanted, and the washing is
repeated at least twice more. If the crystallization and purification were
satisfactory, long, red lycopene prisms are observed under the microscope.
No colorless substance should be present. The centrifuge tube and its con-
tents are dried in vacuo at room temperature for a few hours and then
weighed. The yield, which is dependent on the quality of the tomato paste, is
about 1.5 mg.
a. Color reactions
1. Lycopene dissolves in concentrated sulfuric acid, imparting to the solu-
tion an indigo blue color.
2. On adding a solution of antimony trichloride in chloroform to a solution
of lycopene in chloroform, an intense unstable blue color is produced.
b. Lycopene—(All trans.)
17 18 19 20
13
C NMR
C-l 131 64 C-8 135.54 c - 15 130.17
C-2 124 12 C-9 136.15 c - 16 25.66
C-3 26 83 C-10 131.64 c - 17 17.70
C-4 40 30 C-ll 125.21 c - 18 16.97
C-5 139 30 C-12 137.46 c - 19 12.90
C-6 125 94 C-13 136.54 c - 20 12.81
C-7 124 87 C-14 132.71
I. Carotenoids 117
1
d. HNMR[220MHz-CDCI3]
H-2 H-3/H-4 H-6
05.11 2.11 5.95
H-7 H-8 H-10
6.49 6.25 6.19
H-11 H-12 H-14 H-15
6.64 6.35 6.23 6.63
e. Mass spectrum
Lycopene C 4 0 H 5 6 , Mol . wt 536.
m/z 536(21.70%) 105(47%) 81(36%)
145(38%) 93(36%) 69(100%)
119(34%) 91(47%) 41(57%)
f. UV spectrum of lycopene
λ EmtaOx H 443,472,504 ιημ.
Lycopene is a polyene with 11 conjugated C = C double bonds (22 π-
electrons). With an increase in the number of 7r-electrons in such a system,
there is a bathochromic shift of the longest band, which in the case of
carotenoids reaches the visible part of the spectrum.
References
1. Hartsen (1873). Compt. rend. 76, 385.
2. Karrer, P., Rubel, F . , and Strong, F . M. (1936). Helv. Chim. Acta 19, 28.
3. Kuhn, R . , Bielig, Η., and Dann, Ο. (1940). Ber. 73, 1080.
4. Willstätter,, R . and Escher, H. H. (1910). Z. Physiol. Chem. 64, 47.
5. Porter, J . W. and Zscheile, F . B . (1946). Arch. Biochem. 10, 537.
6. Tan, B . J . (1988). Food Sei. 53, 954.
7. Sandoval, Α . , and Zechmeister, L. (1949). Biochem. Prepns. 1, 57.
Recommended Review
1. Goodwin, T . W. (1962). Carotenoids, structure, distribution, and function. In "Comparative
Biochemistry," (M. Florkin, and H. S. Mason, eds.), Vol. 4, p. 643. Academic Press, New
York.
D. Thin-Layer Chromatography of Carotenoid Pigments

in Oranges
1. Introduction
The complete analysis of carotenoid pigments involves extraction, saponifica-
tion, separation by chromatographic methods and, finally, identification of
each pigment. Using T L C , the preliminary fractionation into hydrocarbons,
monools, diols and polyols is effected on silica-gel plates developed with the
solvent system acetone-petroleum ether ( 3 : 7 ) . Each group can be further
separated into individual carotenoids by rechromatography on MgO-Kiesel-
gur (1:1) plates using the above solvent system and increasing the amount of
acetone according to group polarity.
2. Principle
In the following procedure (1) orange peels are blended with acetone in the
presence of B H T (an antioxidant) and calcium carbonate (a neutralizing
agent).
The extract of cartenoids is then saponified and the free carotenoids
separated on thin layers of MgO-Kieselgur plates. Their identity is deter-
mined by chromatographic (Rf values) and spectroscopic data.
3. Apparatus
Ultra Turrax Homogenizer
UV-Vis Spectrophotometer
T L C applicator
4. Materials
Acetone Magnesium oxide (for T L C )
Butylated hydroxytoluene ( B H T ) Methanol
Calcium carbonate Orange peels
Chloroform Petroleum ether
Diethyl ether Potassium hydroxide
Ethanol, absolute Silica gel-coated T L plates
Kieselgur (for T L C ) Sodium chloride
5. Time
6 hours
6. Procedure
a. Extraction
Orange peels (20 g) or other material are homogenized—cooling with ice, in
an Ultra Turrax homogenizer—with acetone in the presence of B H T as
antioxidant and calcium carbonate as neutralizing agent. After filtering under
reduced pressure, the residue is re-extracted with the same solvent until
colorless. The acetonic extract is mixed with an equal volume of diethylether
(peroxide-free), and sufficient saturated saline solution is added to form two
layers. The upper layer (epiphase) contains all the pigments. It is washed
several times with distilled water.
I. Carotenoids 119
b. Saponification and removal of sterols

The diethylether pigment extract is evaporated to dryness in vacuum (at
40°C), absolute ethanol being added to remove the water. The residue is
extracted with diethylether ( 2 - 3 ml), and an equal volume of 1 0 % K O H in
ethanol is added. The mixture is kept for 2 - 3 hr in a nitrogen atmosphere at
room temperature. After diluting with ether, the ethereal solution is washed
free of alkali and evaporated in vacuum. The amount of total carotenoids is
determined by spectroscopy. The nonsaponifiable matter is dissolved in a
minimal volume of methanol and kept overnight in a freezer at - 2 0 ° C , during
which period the sterols precipitate. They are removed by centrifugation in a
refrigerated centrifuge.
c. TLC
After evaporation of the methanolic supernatant solution under reduced
pressure, the residue is dissolved in a few drops of chloroform and petroleum
ether. The extract is applied as a line on a silica-gel plate (0.4 mm thick),
which is developed with 3 0 % acetone in petroleum ether. When the upper
band of carotenes reaches a distance of 2 cm from the top of the plate, it is
rapidly scraped off into a beaker containing acetone. The plate is further
developed with 3 0 % acetone in petroleum ether until a good separation of all
zones is obtained.
Each band is further rechromatographed on thin layers of M g O - K i e -
selgur ( 1 : 1 ) . The less-polar band is developed with 2 to 5 % acetone in pe-
troleum ether. Thus, phytofluene and α-, β- and γ-carotene are readily
separated and identified by their visible color: phytofluene shows blue-green
fluorescence in U V light, α-carotene shows yellow; ß-carotene shows orange;
and γ-carotene shows lemon yellow.
The monol group is developed with 1 0 % acetone in petroleum ether,
and the more polar groups of diols and triols with 3 0 % acetone in petroleum
ether.
Identification of the pigments and colorless polyenes is made on the
basis of their chromatographic and spectroscopic properties. The absorption
spectrum of each pigment is recorded in a D B Spectrophotometer in the
range of 220 to 550 nm (see table below).
Visible Absorption Maxima of Carotenoids
Carotenoid Ethanol (nm) Carotenoid Ethanol (nm)
Phytofluene 327, 348, 367 Lutein 420, 443, 472

α-Carotene 420, 443, 372 Zeaxanthin 425, 450, 478
/3-Carotene 425, 450, 475 Anteraxanthin 418, 444, 470
γ-Carotene 378, 400, 424 Luteoxanthin 400, 424, 448
ΟΗ-α-Carotene 418, 440, 468 Violaxanthin 416, 438, 468
Cryptoxanthin 425, 450, 475 Citraurin 454
For some functional groups, chemical tests, like the epoxide test and the
carbonyl-reduction test, may be used.
d. Epoxide test
Isomerization of the 5,6 epoxides into 5,8 epoxides occurs rapidly even in the
presence of a trace amount of a mineral acid. The reaction is very fast, and
the rearrangement produces a hypsochromic shift in the visible absorption
spectrum as the chromophore is shortened.
e. Carbonyl reduction test

The reduction of the carbonyl function can be carried out with LiAlH 4 in
ether or N a B H 4 in ethanol. A hypsochromic shift of about 6 to 7 nm is
indicative of an in-ring carbonyl. A shift of 25 to 35 nm indicates an in-chain
carbonyl.
Reference
1. Ikan R . , (1982). "Chromatography in Organic Microanalysis." Academic Press, New York.
Recommended Reviews
1. Gross, J . (1980). A rapid separation of citrus carotenoids by thin-layer chromatography.
Chromatographia 13, 572.
2. Stewart, I. (1980). Color as related to quality in citrus. In: "Citrus Nutrition and Quality"
(S. Nagy, and J . A . Attaway, eds.), p. 129. American Chemical Society Symp. Series 143.
E. High-Performance Liquid Chromatography

of Carotenoids in Orange Juice
1. Introduction
Certain carotenoids such as /3-cryptoxanthin and a- and ß-carotene are highly
colored compounds that also exhibit provitamin A activity. ß-Carotene has
the highest vitamin A activity because it can be split through central enzy-
matic cleavage into two molecules of vitamin A. Because of structural
differences in part of the molecule, only half of each molecule of a-
carotene, γ-carotene and ß-cryptoxanthin has the required intact ß-ionone
ring structure for vitamin A activity. (1) Therefore, these carotenes exhibit
I. Carotenoids 121
lower vitamin A activity. Nevertheless, they are important dietary sources of

vitamin A.
Carotenoids, located in juice vesicle plastids, are also the major source
of color in orange juice and as such are an important quality factor. Orange
juices with the expected deep, yellow-orange color are preferred by most
consumers and may even be perceived as being sweeter.
2. Principle
The following method (2) may be used to analyze the citrus juice carot-
enoids for taxonomy and regulatory or quality-control studies. It is based on
methanol extraction of carotenoids from centrifuged juice solids. A C 1 8 solid-
phase extraction column is used to clean up the saponified sample before
HPLC analysis. Nonaqueous re versed-phase HPLC employing acetonitrile-
methylene chloride-methyl alcohol mixture and a C 1 8 column is used to sep-
arate /3-cryptoxanthin and a- and ß-carotene from other juice components.
3. Apparatus
Centrifuge
High-pressure liquid Chromatograph
Magnetic stirrer
4. Materials
Acetonitrile Orange juice
Ethyl acetate Potassium hydroxide
Methanol Syringe
Methylene chloride Zerbax ODS column
5. Time
3 hours
6. Procedure
a. Sample preparation
A 10 ml sample of orange juice is centrifuged for 5 min at 3000 g. This
operation produces a pellet containing the carotenoids. The clarified juice is
then decanted and discarded, and the wet pellet is stirred with 2 ml methanol.
The slurry is recentrifuged, and the supernatant, discarded. The pellet is then
extracted with 3 ml methanol using an Omni-Mixer. The resulting slurry is
centrifugea, and the supernatant, saved. This operation is repeated two more
times, and the methanol extracts are combined. All work with extracted
carotenoids is done under nitrogen and subdued light.
b. Saponification
Methanolic potassium hydroxide, 4.5 ml, (of 10 g/100 ml methanol solution)
is added to the combined methanol extracts of carotenoids, and the resulting
mixture is allowed to stand in the dark without stirring for 1 hr at 23°C. The
yellow reaction mixture is transferred to a 125-ml separatory funnel with
30 ml methylene chloride. The potassium hydroxide is removed by washing
with 4 x 20 ml water. The yellow organic layer containing the carotenoids is
evaporated to dryness under nitrogen at 35°C.
c. Sample cleanup
The above residue is dissolved in 2 ml methanol and placed on the top of a
6-ml C 1 8 extraction column preconditioned with 5 ml methanol. A syringe
with an adapter is used to push the liquid slowly through the column. The
absorbed carotenoids are then eluted with 4.5 ml methanol-water ( 9 5 : 5 ; v/v;
fraction 1), followed by 3 ml methylene chloride (fraction 2). Each fraction is
separately evaporated to dryness. The resulting two residues are each redis-
solved in 2 ml of the chromatographic mobile phase (acetonitrile-methylene
chloride-methanol; 6 5 : 2 5 : 1 0 ) and placed in an amber 4-ml vial before injec-
tion into HPLC apparatus.
d. HPLC conditions
Zorbax ODS analytical column (4.6 mm x 250 mm) is used with the following
solvent system:
1. acetonitrile-methylene chloride-methanol ( 6 5 : 2 5 : 1 0 ) ;
2. acetonitrile-methylene chloride-methanol ( 7 0 : 2 0 : 1 0 ) ;
3. acetonitrile-tetrahydrofuran-methanol ( 7 0 : 2 0 : 1 0 ) ; and
4. acetonitrile-ethyl acetate-methanol ( 7 0 : 2 0 : 1 0 ) .
Sample injection volume is 50 μΐ. The eluant is monitored at 450 nm.
Column temperature is kept at 22 to 24°C. Flow rate of the solvent is
1.5 ml/min. After several injections, the column is washed with methylene
chloride and then equilibrated with the mobile phase.
Notes
1. Since the carotenoids of interest are of similar polarity, an isocratic
rather than a gradient system for the HPLC is used.
2. The first washing of the wet pellet with methanol removes most of the
water and only the most polar materials. Only the second methanol
extract solubilized a- and /3-carotenes and cryptoxanthin.
I. Carotenoids 123
3. The first water wash from the saponified sample is yellow. The color is
probably due to the presence of chalcones formed by the reaction of
potassium hydroxide and juice flavanones. Acidification of the yellow
fraction results in a colorless solution, which is typical of chalcones but
not of carotenoids.
4. If desired, the cryptoxanthin can be separated from the carotenes on
the solid-phase extraction column by eluting with 9 7 % methanol-3%
water instead of methylene chloride.
5. The time required from the collection of a single juice to final
carotenoid concentration values is about 4 hr. The majority of the time
savings is owing to a 1-hr saponification step and the employment of
an isocratic chromatographic system.
6. Chromatographic peaks are identified by chromatographic
characteristics using standard carotenoids and spectroscopic data. A
small absorbance band at 365 nm may be due to the minor presence
of the cis-isomer of ß-carotene.
References
1. Goodwin, T. W. (1980). The Biochemistry of the Carotenoids, England. Chapman and Hall,
Vol. 1.
2. Fisher, J . F . , and Rouseff, R . L. (1986). J. Agric. Food Chem. 34, 9 8 5 - 9 8 9 .
Recommended Reviews
1. Ruedi, P. (1985). H P L C — a powerful tool in carotenoid research. Pure Appl. Chem. 57,
793.
2. Nelis, H . J . C F . , and DeLeenheer, A . P . (1983). Isocratic nonaqueous reverse-phase liquid
chromatography of carotenoids. Anal. Chem. 55, 270.
3. Schwartz, S. J . , and von Elbe, J . H. (1982). H P L C of plant pigments. J. Liq. Chrom. 5, 43.
F. Determination of ß-Carotene and Chlorophylls in Plants

1. Introduction
All green plant tissues contain a mixture of carotenes, xanthophylls, and
chlorophylls. A variety of solvents may be used to extract these pigments,
acetone and methanol being those most commonly employed. If fresh tissues
are used, they are frequently shredded with the solvent in a blender, or
ground together with the extractant and sand in a mortar. This should be
carried out in dim light. Heating should be avoided during the extraction
stage, as the pigments have a tendency to undergo rapid oxidation and
isomerization when exposed to heat and light (1).
Using a properly activated adsorbent, the separation of the carotenes

from the xanthophylls and other noncarotene pigments becomes a relatively
simple matter. The absorption spectrum of a pigment, together with its
adsorptive power or relative position on a chromatographic column, provides
a good indication of its identity. Various adsorbents have been used for the
separation of chloroplast pigments. These include aluminum oxide, magne-
sia, inulin, starch, cellulose ( 2 - 4 ) , calcium phosphate ( 5 ) , polyethylene ( 6 ) ,
hydrated limes ( 7 ) , and powdered sugar (8).
2. Principle
After the pigments have been extracted, chlorophyll can be determined by
various methods based on colorimetry, spectrophotometry, fluorimetry, and
estimation of magnesium. The spectrophotometric determination of chloro-
phyll is in accordance with the Beer-Lambert law, and various equations have
been derived for determining the concentration of total chlorophyll and of
chlorophylls a and b separately (9,10).
In the following procedure (11), the crude plant extract is introduced at
the top of the column filled with magnesia and diatomaceous earth, 1:1, and
eluted with a mixture of acetone-hexane, 1:9. The purified carotenes are
then collected and determined spectrophotometrically, while chlorophylls
and xanthophylls remain on the adsorbent.
3. Apparatus
Blender
Colorimeter
4. Materials
Acetone Magnesia
Diatomaceous earth Magnesium carbonate
Hexane Sodium sulfate
5. Time
3 - 4 hours
6. Procedure
a. Extraction
A 2- to 5-g sample of the fresh tissue is placed in a high-speed blender, and
40 ml acetone, 60 ml hexane, and 0.1 g magnesium carbonate are added. The
I. Carotenoids 125
mixture is blended for 5 min, filtered on a Büchner funnel, and washed with
25 ml acetone and 25 ml hexane. The extractions are transferred to a separa-
tory funnel and washed with five 100-ml portions of water. The upper layer is
transferred to a 100-ml volumetric flask containing 9 ml acetone and made up
to the mark with hexane. Alcohol (80 ml in conjunction with 60 ml hexane)
may be used instead of acetone for extraction.
b. Determination of chlorophyll
According to this method, the chlorophyll is measured in the original extract
in the presence of all the extracted yellow pigments. A portion of the original
extract (regardless of the solvent used) is placed in the absorption cell of a
photoelectric colorimeter, and the transmission of the solution is compared
with that of the pure solvent.
The transmission of the solution is converted to concentration by means
of a standard calibration curve obtained with pure chlorophyll. A red filter or
a combination of filters transmits radiation in the region in which chlorophyll
has maximal absorption, thus making possible a precise measurement of
chlorophyll concentration.
c. Determination of 0-carotene
The chromatographic column (2 x 18 cm) is packed to a height of 15 cm with
1:1 mixture of activated magnesia and diatomaceous earth, the adsorbent is
gently compacted, and a 1-cm layer of anhydrous sodium sulfate is placed
above the adsorbent. The extract is poured into the column and developed
with 50 ml acetone-hexane ( 1 : 9 ) , or more if necessary, to wash the visible
carotenes through the adsorbent. The top of the column should be covered
with a layer of solvent throughout the operation. The carotenes pass rapidly
through the column, and the bands of xanthophylls, carotene oxidation
products, and chlorophylls should remain on the column when the develop-
ment is complete. The eluate is transferred to a 100-ml volumetric flask and
made up to the mark with acetone-hexane, 1:9. The carotene content is
determined photometrically. When determinations are made with a properly
calibrated spectrophotometer at 436 m/i, the concentration of /3-carotene is
given by the following formula,
absorbance x 454
C
" 196 x L x W
where, C = concentration of carotene (mg/lb) in original sample; L = cell

length in cm; W = gram sample/ml final dilution.
The results are reported as mg ß-carotene/lb or multiplied by 2.2 to
give ppm.
References
1. Zechmeister, L. (1958). Chem. Revs. 34, 267.
2. Duranthon, J . , Galmiche, J . M., and Roux, Ε . (1958). C R . Acad. Sei. Paris 246, 992.
3. Laborie, Μ. Ε . (1963). Ann Physiol. Veg. 5, 89.
4. Angapindu, Α . , Silberman, H., Tantivatana, P., and Kaplan, I. R . (1958). Arch. Biochem.
Biophys. 75, 56.
5. Moore, L. A. (1940). Ind. Eng. Chem., Anal. Ed. 12, 726.
6. Anderson, A . F . H . , and Calvin, M. (1962). Nature (London) 194, 285.
7. Bickoff, Ε . M., Atkins, Μ. E . , Bailey, G. F . , and Stitt, F . (1949). J. Am. Offic. Agric.
Chemists 32, 766.
8. Perkins, H. J . , and Roberts, D . W. A. (1962). Biochim. Biophys. Acta 58, 486.
9. Maclachlan, S., and Zalik, S. (1963). Can. J. Bot. 4 1 , 1053.
10. Bruinsma, J . (1961). Biochim. Biophys. Acta 52, 576.
11. Assoc. Offic. Agric. Chemists, (1960). p. 654. Washington 4, D . C .
Recommended Reviews
1. Holden, M. (1965). Chlorophylls. In "Chemistry and Biochemistry of Plant Pigments,"
(T. W. Goodwin, ed.), pp. 462. Academic Press, New York.
2. Davies, Β . H. (1965). Analysis of carotenoid pigments. In Chemistry and Biochemistry of
Plant Pigments. ( T . W. Goodwin, ed.), p. 489. Academic Press, New York.
G. Questions
1. Which are the main natural sources of carotenoids?

2. How can one prove the structure of a carotenoid?
3. Which methods may be used for trans -> eis isomerization of
carotenoids?
4. Why should considerable amounts of yellow vegetables and green leafy
plants be included in the diet?
5. How are zeaxanthin, lutein, and capsanthin related to a- and
ß-carotenes?
6. What is the biogenetic relationship between carotenoids and
terpenoids? Outline the biosynthesis of lycopene.
H. Recommended Books
I. Bauernfeind, J . C , (1981). "Carotenoids as Colorants and Vitamin A.

Precursors." Academic Press, New York.
2. Goodwin, T. W. (1954). "Carotenoids." Chemical Publishing Co.,
New York.
II. Steroids 127
3. Goodwin, T. W. (ed.) (1965). "Chemistry and Biochemistry of Plant

Pigments" Academic Press, New York.
4. Karrer, P. and Jucker, E . (1950). "Carotenoids," Elsevier, New York.
5. Krinsky, Ν. I. (1990). "Carotenoids, Chemistry and Biology," Plenum,
New York.
6. Liaaen-Jensen, S. (1980). Stereochemistry of natural carotenoids.
Prog. Chem. Org. Nat. Prod. 39, 123.
7. Rando, R . B . (1990). The chemistry of vitamin A and vision. Angew.
Chem. Int. Ed. 19, 461.
II. STEROIDS
A. Introduction
Many naturally occurring substances, such as sterols, bile acids, sex hor-
mones, adrenal cortical hormones, cardiac glycosides, toad poisons and
sapogenins, contain the cyclopentanoperhydrophenanthrene ring system or,
in very rare cases, a modification of it.
The sterols are widely distributed in nature. They are found both in the
free state and combined as esters or glycosides. Very often they occur in the
form of complex mixtures, the components of which are difficult to separate.
Paper, column, thin-layer and vapor-phase chromatography make possible
the qualitative and quantitative analysis of sterols and steroids. Other
methods are ultraviolet and infrared spectra, rotatory dispersion, nuclear
magnetic resonance, X-ray crystallographic analysis, and mass spectroscopy.
Most of the steroids are hydroxylated at C 3 , while some also have OH
groupings in other positions of the ring system or the side chain. In choles-
terol and cholestanol, the—OH group on C 3 is on the same side as the
— C H 3 group on C 1 0 , i.e., both project toward the front of the molecule
(/3-orientation). When the OH of C 3 lies on the side of the ring opposite to
that of the — C H 3 at C 1 0 , the configuration at C 3 is a. The stereochemistry of
the side chain, the angular methyl groups, and the B / C and C / D trans ring
fusions of bile acids is the same as that of cholestanol. The only difference is at
C 5 , since the bile acids are A / B - c i s (5/3) compounds, while the sterols are
A / B - t r a n s (5a) compounds.
5α 5β
Cholestanol contains three fused cyclohexane rings, A, B , and C, and a

terminal cyclopentane ring. Rings Β and C are locked in the chair conforma-
tion by transfusion to rings A and D. In coprostanol, rings B , C, and D are
the same as in cholestanol, but ring A is cis-fused and has a chair conforma-
tion. The conformational representations of cholestanol and coprostanol are
presented in the following figures:
Cholestanol
A number of general rules governing the stability and reactivity of

equatorial and axial positions have been elaborated, mainly by Barton.
1. Sterols
Cholesterol is one of the most abundant compounds. It is present in verte-
brates and invertebrates and was recently found in plants. Cholesterol is often
II. Steroids 129
accompanied by closely related sterols such as cholestan-3-/3-ol, coprostan-

ß-ol, and others.
21
Lathosterol
The main steps in the biosynthesis of cholesterol are the conversion of

acetate to squalene, the concerted cyclization of squalene to lanosterol, and
the demethylation of lanosterol to cholesterol.
a. Sterols of marine invertebrates

The sterols in the lower forms of animal and plant life are of interest, as they
suggest a relationship between the stage of evolution and the type of sterol
formed. In many sterols of invertebrates, the eight-carbon side chain of
cholesterol is replaced by a nine-carbon unit with a methyl branch at C 24 or a
10-carbon unit with an ethyl group.
The typical marine sterols are
Spongesterol Clionasterol
24-Methylenecholesterol Fucosterol
b. Plant sterols
Sitosterol and stigmasterol are the most abundant plant sterols and occur in
complex mixtures; they also have C 9 or C 1 0 side chains.
Stigmasterol Brassicasterol
II. Steroids 131
c. Yeast sterols
The most abundant sterols of this type are ergosterol and zymosterol.
Ergosterol Zymosterol
Ascosterol and fecosterol rank among the minor yeast sterols.
Ascosterol Fecosterol
2. Bile Acids
Bile acids are isolated from the bile of higher animals, where they are found
as sodium salts of peptidic conjugates with taurine and glycine. In all these
acids the hydroxyl groups are α-oriented, and the juncture of rings A and Β is
eis. The side chain is usually made up of five carbon atoms and bears the
carboxyl group. The bile acids resemble cholestanol in the orientation of the
side chain and of the angular methyl groups in the B / C and C / D ring fusion.
There are two main classes: C 27 _ 2 8 acids and C 24 acids. The C 27 _ 2 8 acids have
3α,7α,12α -Trihydroxycoprostanic acid Cholanic acid

been found in the bile of reptiles and amphibia. The best known are the 25a-
and β-isomers of 3a, la, 12a-trihydroxycoprostanic acid. Turtle and tortise
bile contains tetrahydroxysterocholanic and tetrahydroxyisosterocholanic
acids, probably C 2 7 H 4 6 0 6 .
Numerous naturally occurring, substituted cholanic acids are known,
such as:
Cholic acid Desoxycholic acid
Lithocholic acid
The salts of the bile acids lower the surface tension of water and are
good emulsifying agents. It has been shown that bile acids are made in the
liver mainly from cholesterol.
3. Steroid Hormones
Hormones are substances secreted by specific glands, and exert control over
various body processes. The steroid sex hormones are divided as follows:
female hormones, such as the estrogens (estradiol, estrone, and estriol); pro-
gestational hormones, such as progestrone; and androgens—testosterone
and androsterone—that have male hormone activity.
The naturally occurring estrogens differ from other steroid hormones in
the presence of an aromatic ring A , the absence of a methyl group at C 1 0 , and
the presence of a keto- or hydroxy- group at position 17 and sometimes at
position 16.
II. Steroids 133
Estriol Progesterone
The adrenocortical hormones have 21 carbon atoms, ketonic groups at

C 3 and C 2 0 , a double bond at the 4(5)-position, and a hydroxyl group C 2 1 .
These compounds may be divided into the highly active glucocorticoids, e.g.,
cortisone and hydrocortisone, and highly active mineralocorticoids, e.g.,
desoxycorticosterone and aldosterone.
C H 2O H C H 2O H
Cortisone Cortisol
C H 2O H
11- Dehydrocorticosterone
C H 2O H OH C H 2O H
ι l l
Aldosterone
The naturally occurring androgens such as androsterone have 19 car-

bon atoms. The principal androgenic steroid is the male sex hormone
testosterone.
Testosterone
Androsterone
Recently, a series of steroidal insect-molting hormones, such as ecdy-

sone, was discovered.
OH
Ecdysone
4. Cardiac-Active Principles
Certain steroids exert a specific and powerful effect on the cardiac muscle and
are called cardiac-active (cardiotonic) principles. Many cardiac glycosides
have been isolated from plants in tropical regions and have been employed by
natives of Africa and South America for the preparation of arrow poisons.
Some occur in the secretions of poisonous toads. The aglycons are of two
types: cardenolides and bufadienolides. The cardenolides are C 2 3 steroids
II. Steroids 135
having as side chain an a, ^-unsaturated, five-membered lactone ring and a

C 1 4 hydroxyl group. They may be exemplified by the following:
Sarmentogenin
The bufadienolides are C 2 4 steroids having as side chain a doubly

unsaturated, six-membered lactone ring and a 14/3-hydroxyl group or its
modification.
Bufalin Marinobufagin
5. Sapogenins
Plant glycosides that have the property of forming a soapy lather in water are
called saponins. One of them, digitonin, is used for selective precipitation of
3 ß-hydroxy steroids. The following are examples of sapogenins, the sugar-free
moieties of the saponins:
Cholegenin
H
Tokorogenin
Β. Isolation of Stigmasterol from Soybean Oil
Stigmasterol
1. Introduction
Stigmasterol was first isolated by Windaus and Hauth (1) from the seeds of
Physostigma venenosum, the Calabar bean. Other sources are rice bran fat
(2), soybeans (3), coffee oil (4), ergot oil (5), tea oil (6), flue-cured tobacco
leaves ( 7 ) , dried potatoes ( 8 ) , coconut oil (9), and many other plants.
Recent investigation of the steroid constituents of soybean oil (11) by
gas-liquid chromatography has revealed, in addition to stigmasterol, the
presence of campesterol and ß-sitosterol.
2. Principle
The following procedure (10) consists of saponification of crude soybean oil.
Ether is used to extract the unsaponifiable materials. The ether is then
distilled off and replaced by petroleum ether saturated with steam, whereup-
on the crude sterol fraction is precipitated. It is then acetylated and bromi-
II. Steroids 137
nated. The resulting stigmasteryl acetate tetrabromide is sparingly soluble in

acetic acid, acetone, and ether, and can be separated from the far more
soluble sitosteryl acetate dibromide. The bromine is then removed by treat-
ment with zinc dust, and the acetate is hydrolyzed with alcoholic potassium
hydroxide. Stigmasterol is obtained by crystallization from 9 5 % ethanol
solution.
3. Apparatus
Steam Bath
4. Materials
Acetic acid Ethanol, absolute Sodium carbonate
Acetic anhydride Ether Sodium sulfite
Bromine Methanol Soybean oil
Chloroform Petroleum ether Zinc dust
Ethanol, 9 5 % Potassium hyroxide
5. Time
9-10 hours
6. Procedure
a. Isolation
To 165 g crude soybean oil are added 800 ml absolute ethanol and 150 g
potassium hydroxide dissolved in a minimal volume of water. This mixture is
placed in a 2-liter round-bottomed flask fitted with a condenser and refluxed
for 2 hr on a steam bath. After saponification, 800 ml water is added, and the
solution is extracted with ethyl ether (5 x 300 ml). The extraction of the
unsaponifiable materials from the soaps is accomplished by stirring the mix-
ture for an hour with an air stirrer, allowing the ether layer to separate, and
siphoning off the ether. The extracts are concentrated to about half their
original volume and washed free of alkali with distilled water. The remainder
of the solvent from the ether extraction is then distilled under reduced
pressure at about 40°C. The residue—the unsaponifiable material—is dis-
solved in 100 ml petroleum ether (bp 40-60°C), and steam is passed into the
solution until the saturation point is nearly reached. The solution is allowed to
stand overnight. A precipitate consisting of about 1 g colorless crystals of mp
138-144°C is obtained.
b. Acetylation
The crude material is acetylated with 20 ml acetic anhydride by refluxing for
\ \ hr. The mixture is then cooled for 1 hr at 20°C, and the crude acetates are
filtered.
c. Bromination
One g of the acetates is dissolved in 10 ml ethyl ether, and to this solution is
added 12 ml bromine-acetic acid solution (5 g bromine in 100 ml glacial acetic
acid). After cooling, the insoluble tetrabromides are filtered off and washed
with cold ethyl ether. About 300 mg of mp 190-194°C is obtained. The
bromides are recrystallized from chloroform-methanol; mp of crystals 1 9 4 -
196°C.
d. Debromination
To a solution of 300 mg recrystallized bromides in 4 ml glacial acetic acid is
added 300 mg zinc dust. The mixture is refluxed for 1 \ hr, filtered hot, diluted
with about 10 ml water, and extracted with ethyl ether. The ethreal solution is
washed with dilute aqueous sodium sulfite solution, then with water, and the
ether is removed by evaporation. The product obtained weighs about 150 mg.
It is recrystallized once from ethanol and then from methanol-chloroform,
2 : 1 ; mp 139-140°C.
e. Stigmasterol
Stigmasteryl acetate (100 mg) is hydrolyzed for 1 hr with about 10 ml 1 0 %
alcoholic potassium hydroxide. About 10 ml water is added, and the mixture
is extracted with ethyl ether. The ethereal solution is washed with dilute aque-
ous sodium carbonate and then with water. After removal of the ether, the
residue is recrystallized three times from 9 5 % ethanol. About 30 mg of the
product is obtained; mp of crystals 168-169°C.
f. Stigmasterol
29
,CH 3
HO'
13
g. C NMR [CDCy
C-l 37.31 C-4 42.35 C-7 31.94
C-2 31.69 C-5 140.80 C-8 31.94
C-3 71.81 C-6 121.69 C-9 50.20
II. Steroids 139
C-10 36.56 C-17 56.06 C-24 51.29

C-ll 21.11 C-18 12.07 C-25 31.94
C-12 39.74 C-19 19.42 C-26 21.26
C-13 42.35 C-20 40.54 C-27 19.02
C-14 56.91 C-21 21.11 C-28 25.44
C-15 24.39 C-22 138.37 C-29 12.27
C-16 28.96 C-23 129.32
h. Mass spectrum
Stigmasterol C 2 9 H 4 8 0 , Mol wt. 412.
m/z 412(29%) 83(65%) 55(100%)
271(75%) 81(75%) 43(64%)
93(50%) 69(58%) 41(58%)
i. UV spectrum of stigmasterol
A S S " 204 τημ (loge 3.58)
Stigmasterol is a diene with two isolated double bonds. Thus, absorption in
the far U V region cannot be measured with the normal spectrophotometer,
but only in vacuo.
References
1. Windaus, A. and Hauth, A. (1906). Ber. 39, 4378.
2. Nebenhauer, F . P., and Anderson, P. J . (1926). J. Am. Chem. Soc. 48, 2972.
3. Thornton, M. H., Kraybill, H. R . , and Mitchell, J . H. (1940). / . Am. Chem. Soc. 62, 2006.
4. Bauer, Κ. H., and Neu, R. (1944). Fette und Seifen 5 1 , 343.
5. Ruppol, Ε . (1949). J. Pharm. Belg. 4, 55.
6. Goguadze, V. P. (1950). Izvest. Akad. Nauk SSSR, Otdel Khim. Nauk 185.
7. Grossman, J . D., and Stedman, R. L. (1958). Tobacco 147, ( 1 1 ) , 22.
8. Schwartz, J . J . , and Wall, M. E . (1955). J. Am. Chem. Soc. 77, 5442.
9. Andersen, B , and Krawack, B . (1957). Acta Chem. Scand. 11, 997.
10. Byerrum, R . U., and Ball, C. D. (1960). Biochem. Prepns. 7, 86.
11. Thompson, M. J . , Robbins, W. E . , and Baker, G. L. (1963). Steroids 2, 505.
Recommended Review
1. Daubert, B . F. (1950). Chemical composition of soybean oil. In "Soybeans and Soybean
Products" (K. S. Markley, ed.), Vol. 1, p. 157. Interscience, New York.
C. Degradation of Stigmasterol
1. Introduction
Windaus, Werber, and Gschaider (1) have established the empirical formula
of stigmasterol as C 2 9 H 4 8 0 . Guiteras (2) isolated ethylisopropylacetaldehyde
as a product of ozonization of stigmasterol, and established the presence

of an ethyl group at C 2 4 and a double bond at C 2 2 = C 2 3 . The position of
the hydroxyl group was established by Fernholz and Chakravorty (3) by chro-
mic acid oxidation of stigmastanyl acetate and isolation of 3/3-acetoxy-
bisnorallocholanic acid.
COOH
Pt/C
Ether-AcOH
Ac Ο AcO-
Stigmasteryl acetate 3-Acetoxy-bisnorcholenic acid
H3C\ /COOH H3C\ /COOH

H 3c H 3C
KOH CrQ3
EtOH AcOH
HO
3-Acetoxy-bisnorcholanic acid 3-Oxy-bisnorallocholanic acid
COOH H3C^ /COOH

H 3C
Zn/Hg H 3C
AcOH
3-Keto-bisnorallocholanic acid Allocholanic acid
2. Principle
In the following degradation ( 4 ) , stigmasteryl acetate is brominated to form
the 5,6-dibromide. Subsequent ozonization and debromination with zinc in
5
acetic acid yields 3/3-acetoxy-A -bisnorcholenic acid, which is converted by
catalytic hydrogénation, alkaline hydrolysis, oxidation with chromic acid, and
Clemmensen reduction to bisnorallocholanic acid.
3. Apparatus
Catalytic hydrogénation apparatus
Ozonator
II. Steroids 141
4. Materials
Acetic acid Ozone
Acetic anhydride Potassium hydroxide
Acetone Platinum on charcoal ( 5 % )
Bromine Pyridine
Chloroform Sodium hydroxide
Chromium trioxide Stigmasterol
Dioxane Sulfuric acid
Ethanol Xylene
Ether Zinc, amalgamated
Hydrochloric acid Zinc, dust
Methanol
5. Time
15 hours
6. Procedure
a. Stigmasteryl acetate
Stigmasterol (5 g), 20 ml acetic anhydride, and a few drops of pyridine are
refluxed for 1 hr. After cooling, methanol is added to hydrolyze excess acetic
anhydride, and the solvents are removed under reduced pressure. Stigmas-
teryl acetate is filtered off and crystallized from ethanol as flakes of mp 141°C.
b. 3-Acetoxy-bisnorcholenic acid
To a cold solution of stigmasteryl acetate in 100 ml chloroform is added
dropwise a solution of 2.1 g bromine in 50 ml chloroform. After the addition
is complete, ozone is bubbled through the solution for 2 to 3 hr. Chloroform
is removed under reduced pressure at room temperature, 6 g zinc powder and
100 ml acetic acid are added to the residue, and the mixture is heated on a
steam bath until solution is complete. The solution is then left on a steam bath
for a further period of 1 hr, diluted with water, and extracted with ether. The
ethereal solution is extracted with 2N aqueous sodium hydroxide, whereupon
the sodium salt of the acid separates at the interface. The salt is acidified with
dilute sulfuric acid and extracted with ether. The ethereal solution is then
treated with activated charcoal and filtered, and the ether is distilled off. The
Liebermann-Burchard test gives a yellow color.
c. 3-Acetoxy-bisnorcholanic acid
3-Acetoxy-bisnorcholenic acid (0.8 g) is dissolved in a mixture of ether and
glacial acetic acid and hydrogenated in the presence of platinum on charcoal.
The catalyst is filtered off and the ether is distilled. Addition of water to the
residue precipitates the acid. Recrystallization from dilute acetic acid or from
acetone gives needles of mp 194°C; yield, 0.5 g.
d. 3-Oxy-bisnorallocholanic acid
3-Acetoxy-bisnorcholanic acid (0.52 g) is refluxed for 2 hr with 5 % ethanolic
potassium hydroxide, diluted with water, and acidified with dilute hydrochlo-
ric acid. The acid is filtered off and recrystallized from acetic acid as flakes
of mp 270°C; yield, 0.45 g.
e. 3-Keto-bisnorallocholanic acid
3-Oxy-bisnorallocholanic acid (0.5 g) is dispersed in 20 ml glacial acetic acid,
0.15 g chromium trioxide is added, and the mixture is left in a refrigerator
overnight. The keto acid is precipitated by addition of water, filtered through
a Büchner funnel, and recrystallized from aqueous dioxane as needles, mp
244-246°C; yield, 0.37 g.
f. Allocholanic acid
3-Keto-bisnorallocholanic acid (0.35 g), 20 g amalgamated zinc, and 50 ml
acetic acid are refluxed for 8 hrs. During this period, three 100-ml portions of
concentrated hydrochloric acid and a few ml xylene are added. The cold
solution is diluted with water and extracted with a mixture of ether and
petroleum ether. This solution is shaken thoroughly with 2N aqueous sodium
hydroxide, whereupon the sodium salt is precipitated at the interface. It is
filtered off and acidified with dilute sulfuric acid. Recrystallization from acetic
acid yields plates of mp 214°C.
References
1. Windaus, Α . , von Werber, F . , and Gschaider, B . (1932). Ber. 6 5 , 1006.
2. Guiteras, A . (1933). Z. Physiol. Chem. 214, 89.
3. Fernholz, E . , and Chakravorty, P. N. (1934). Ber. 6 7 , 2021.
4. Fernholz, E . (1933). Ann. 5 0 7 , 128.
D. Isolation and Identification of Algal Sterols

1. Introduction
Since their isolation from prokaryotic organisms, i.e., bacteria (1,2) and
blue-green algae (cyanobacteria) (2,3), sterols have been isolated from all
major groups of living organisms. Cholesterol is the primary sterol of all
higher animals, lower animals may contain cholesterol and/or a complex
mixture of C 2 7- , C 2 8- , and C 2 9-carbon sterols.
II. Steroids 143
In general, sterols of algae differ from those of the higher plants. Most
eukaryotic organisms contain sterols that are used as architectural compo-
nents of the cellular membranes (4), although their roles in reproduction ( 5 ) ,
or other developmental or hormonal roles have been demonstrated in a
number of cases (4). In the higher plants, these sterols are in most cases
5
24a-methyl or 24a-ethyl cholesterol and closely related A -sterols, although
7
recently a few higher plant families have been shown to contain A -sterols
(6,7). Sterols of algae have the 24/3-methyl or 24/3-ethyl configuration ( 8 ) .
The great majority of red algae contain only cholesterol and other
27-carbon sterols as principal sterol components. These sterols have no alkyl
group and thus no asymmetry at C-24. Brown algae contain fucosterol as their
principal sterol. Its 24-ethylidene group eliminates the possibility of α/β
isomers at C-24. Other algal taxa have their own characteristic sterol com-
position; the green algae, as expected, most closely resemble higher plants.
For many years Chlorella, a unicellular green alga, has been an impor-
tant research organism for plant physiologists. In addition, it might be a
source of food for man and domestic animals. The nutritive factors, such as
carotenoids and sterols, of this (and other) algae have received much atten-
tion in recent years.
The first sterol isolated from Chlorella pyrenoidosa was ergosterol (9).
5 7
Sterols with the A ' -double bond system (such as ergosterol) are known to
have provitamin D activity (10).
The species Chlorella ellipsodea and Chlorella saccharophila have been
5
found to contain only A -sterols (11), while Chlorella vulgaris contains only
7
A -sterols (12).
I Chondrillasterol
HO HO
Poriferasterol 28-Isofucosterol
HO HO
Sterols of green algae.
2. Principle
Cell material of a Chlorella species is freeze-dried and extracted with chloro-
form-methanol ( 2 : 1 ) . The lipid obtained is saponified, and the nonsaponifi-
able fraction (NSF) is fractionated on a column of silica gel. The sterol
fraction is acetylated, and the steryl acetates are identified by chromato-
graphic ( T L C , G C ) and spectroscopic techniques. Gas chromatography-
mass spectrometry (GC-MS) is a powerful tool for confirming the structures
5 +
of sterols. In certain steryl acetates (such as the Δ ones), the M peak is ab-
sent in the mass spectrum, and the highest mass-peak appears at M-60.
The experimental part is based on the work of Ikan and Seckbach (13).
3. Apparatus
Gas Chromatograph Soxhlet extractor
Lyophilizer
4. Materials
Acetic anhydride Liquid phases: X E - 6 0 ; D E G S ; OF-1
Algae cells Methanol
Alumina Silver nitrate
Chloroform Thin-layer plates
5. Time
8 hours
6. Procedure
a. Harvesting of algae cells
The algal cells (which may be obtained from a plant physiologist) are har-
vested by centrifugation at 5000 rpm for 10 min, and the pellets are washed in
deionized water to remove traces of soluble nutrients.
b. Extraction of lipids
The algae are extracted with chloroform-methanol ( 2 : 1 ) in a Soxhlet appar-
atus for 3 hr. The extract is filtered and concentrated under reduced pressure,
yielding a green viscous residue.
c. Saponification
The green viscous residue is refluxed for 4 hr with 7% methanolic potassium
hydroxide. The solvent is removed in vacuo, water is added, and the residue
is extracted with ether. Evaporation of ether leaves the NSF.
II. Steroids 145
d. Isolation of sterols
The NSF is dissolved in light petroleum and chromatographed on a silica gel
column (height 15 cm; diameter 1.5 cm). The compounds are eluted with
40 ml of each of the following concentrations of light petroleum in benzene,
10, 25, 5 0 % (v/v), followed by ether and 2 5 % methanol in ether, and finally
with 2 0 % methanol in chloroform. (Carry out the elution of the column in a
well-ventilated hood!). The fractions (15 ml each) are evaporated to dryness.
Examination of each fraction by qualitative T L C (on silica gel GC-254,
developing with light petroleum- ethyl ether- acetic acid, 2 0 : 4 : 1 , and
spraying with 5 0 % H 2 S 0 4 , and charring at 180°C), reveal the presence of
sterols at Rf 0.43. The sterol fractions are pooled and subjected to preparative
thin-layer chromatography (PTLC). The zones of sterols are scraped off the
plates and extracted with chloroform-ethyl ether ( 1 : 1 ) .
e. Steryl acetates
To 50 mg of the isolated sterols, 2 ml of dry pyridine and 0.3 ml of acetic
anhyride is added, and the mixture is allowed to stand at room temperature
overnight (or until the next laboratory work). It is then dissolved in 20 ml
ether and washed in succession with two 20-ml portions each of water, 0.5 Ν
H 2 S 0 4 , 0.5/V NaOH, and again water. Then it is dried over anhydrous
sodium sulfate, filtered, and the ether evaporated.
f. Gas chromatography of steryl acetates

The G C analysis may be carried out in a 6 ft x 0.25 inch glass or stainless steel
column. It may be filled with 3 % SE-52 on 100 to 120 mesh Gas Chrom Ρ and
maintained at 240°C, nitrogen flow, 30 ml/min, on 1% QF-1 on Gas Chrom Ρ
at 275°C, or on 1% D E G S on Gas Chrom Ρ at 205°C. Cholestane is injected
as internal standard.
g. Gas chromatography-mass spectrometry

A Finnigan 400 quadrupole mass spectrometer interfaced with Finnigan gas
Chromatograph with a DB-5 column may be used. Temperature programming
at 4°C/min to 280°C, followed by 2°C/min to 310°C. Em voltage 1500V;
electron energy 70 eV; source temperature 240°C. The compounds are iden-
tified by means of mass spectrometric comparison with standards and by
coinjection of authentic samples.
References
1. Schubert, K . , Rose, G . , Wachtel, H., Hoerhold, C , and Ikekawa, N. (1968). Eur. J.
Biochem. 5, 246.
2. Reitz, R . C , and Hamilton, J . G. (1968). Comp. Biochem. Physiol. 25, 401.
3. D e Souza, N. J . , and Nés, W. R . , (1968). Science 162.
4. Nés, W. R . , and McKean, M. (1977). "Biochemistry of Steroids and Other Isoprenoids."

University Park Press, Baltimore, Maryland.
5. Nés, W. R . , Patterson, G. W . , and Bean, G. A . (1980). Plant Physiol. 66, 1008.
6. Salt, Τ . Α . , and Adler, J . H. (1986). Lipids 2 1 , 754.
7. X u , S., Patterson, G. W . , L u s b y , W . R . , Schmid, Κ. M , and Salt, Τ. A. (1990). Lipids 25,
61.
8. Patterson, G. W. (1971). Lipids 6, 120.
9. Klosty, M., and Bergmann, W. (1952). J. Amer. Chem. Soc. 74, 1601.
10. Fieser, L. F . , and Fieser, M. (1959). "Steroids." Reinhold, New York.
11. Patterson, G . W . , and Krauss, R . W. (1965). PL Cell. Physiol. 6, 211.
12. Ikan, R . , and Seckbach, J . (1972). Phytochem. 11, 1077.
Recommended Reviews
1. Patterson, G. W. (1971). The distribution of sterols in algae. Lipids 6, 120.
2. Thompson, M. J . , Patterson, G. W., Dutky, S. R . , Svoboda, J . Α . , and Kaplanis, J . N.
(1980). Techniques for the isolation and identification of steroids in insects and algae. Lipids
15, 719.
E. Isolation of Hecogenin from Agaves and Its Transformation to

Tigogenin and Rockogenin
1. Introduction
Hecogenin is a sapogenin possessing a keto group at C 1 2 , which can be
transposed to C n , as is the case for the 12-keto bile acids. Hecogenin can
therefore serve as starting material for cortisone preparations.
Hecogenin was first isolated in 1943 by Marker and his coworkers
(1) from several Agave species of Texas, Arizona, California, and Mexico.
Callow, Cornforth, and Spensley (2) found hecogenin in sisal. Gedeon and
Kind (3) have isolated hecogenin together with tigogenin from Agave cantala
and Agave vera-cruz.
Rockogenin was isolated from Agave gracilipes along with large
amounts of hecogenin. The presence of hecogenin together with tigogenin
and rockogenin in certain plants points to their structural similarity.
2. Principle
In the following procedure ( 1 ) , agave is extracted with ethanol. The extract
is treated with acid and alkali to hydrolyze the glycosides and the fatty
esters. Hecogenin may then be characterized by preparation of 2,4-
dinitrophenylhydrazone.
Hydrazine hydrate reduction of hecogenin leads to formation of
tigogenin, while catalytic reduction affords rockogenin. Further correlation
between hecogenin and rockogenin can be established by their transforma-
tion to hecogenone.
II. Steroids 147
CH, O-
HO
Hecogenin
NH2 NH2 H 2/ P t 0 2
CH, O- CH3 o-
HG HO
Tigogenin Rockogenin
3. Apparatus
Catalytic hydrogénation apparatus
4. Materials
Acetic acid Ether
Acetic anhydride Hydrazine hydrate
Acetone Hydrochloric acid
Agaves Methanol
Chromium trioxide Platinum oxide
2,4-Dinitrophenylhydrazine Potassium hydroxide
Ethanol, 9 5 % Sodium, metal
Ethanol, absolute Sodium hydroxide
5. Time
30 hours
6. Procedure
a. Isolation of hecogenin
A 5-kg sample of ground, undried agaves is extracted with 6 liters 9 5 %
ethanol on a steam bath for 12 hr. The slurry is filtered hot and washed with
hot ethanol. The solvent is removed under reduced pressure and the residue
is hydrolyzed by refluxing for 2 hr with 1.5 liter 2N ethanolic hydrochloric
acid. The reaction mixture is cooled and filtered and diluted with 2 liters
ether. The solution is then washed first with water, then with 5 % aqueous
sodium hydroxide, and again with water, and evaporated. The fatty esters are
hydrolyzed by refluxing the residue with three volumes of 10% alcoholic
potassium hydroxide for 30 min. The cooled hydrolysis mixture is extracted
with ether, and the ethereal solution is washed with water and evaporated to a
small volume. The crude sapogenin fraction that separates is dissolved in
acetone and treated with Norit; mp of hecogenin 256-260°C.
b. 2,4-Dinitrophenylhydrazone of hecogenin
To a solution of 0.2 g hecogenin acetate in 30 ml hot ethanol is added a
solution of 0.2 g 2,4-dinitrophenylhydrazine in 50 ml ethanol containing 1 ml
concentrated hydrochloric acid. Within a few minutes, needles start to form.
After standing at room temperature for 3 hr, the crystals are filtered off and
washed with cold ethanol; mp 275-276°C ( d e c ) . Recrystallization from etha-
nol gives orange needles, mp 281-282°C.
c. IR spectrum of hecogenin
- 1
1702 c m : C = 0 stretching (in chloroform)
1055: C—Ο stretching of alcoholic OH (in carbon disulfide)
1250-900: vibrations associated with the spiroketal side chain
(12 bands), (in carbon disulfide)
d. Transformation of hecogenin to tigogenin

To a solution of 3 g sodium in 60 ml absolute ethanol in a bomb-tube are
added 0.5 g hecogenin acetate and 5 ml 8 5 % hydrazine hydrate. The tube is
sealed and heated for 12 hr at 200°C. After cooling, it is opened, and the
reaction mixture is poured into water. The precipitate is taken up in ether.
The ethereal solution is washed with water, dilute hydrochloric acid, and
water, and then concentrated until crystals start to appear. After cooling, the
crystalline material is filtered. Crystallization from methanol gives white
needles, mp 203-206°C; yield, 0.3 g.
e. Transformation of hecogenin to rockogenin

An ethereal solution of 0.3 g hecogenin containing several drops of acetic acid
is shaken with hydrogen and 0.2 g Adams' catalyst for 2 hr at room tempera-
II. Steroids 149
ture and under three atmospheres pressure. After filtering off the catalyst, the
solvent is removed. The oily residue is refluxed with acetic anhydride for 1 hr.
The acetic anhydride is removed in vacuo on a steam bath, and the 12-
dihydrohecogenin diacetate is crystallized from methanol as long needles,
mp 204-206°C; yield, 0.12 g. When hydrolyzed with 5 % alcoholic potassium
hydroxide for 20 min on a steam bath, the diacetate is converted to rockoge-
nin, which crystallizes from methanol as thick needles, mp 208-210°C. R e -
peated crystallization from ether gives crystals of mp 217-220°C.
f. Conversion of hecogenin and rockogenin to hecogenone

A solution of 0.1 g hecogenin in 30 ml acetic acid is mixed with a solution of
0.1 g chromium trioxide in 5 ml 8 0 % acetic acid. After standing 30 min at
25°C, water is added and the product is extracted with ether, washed with
dilute aqueous sodium hydroxide and water, and dried. The ethereal solution
is concentrated and cooled to give white needles, mp 237-240°C. Mild oxida-
tion of rockogenin with chromium trioxide in acetic acid under the conditions
outlined above also gives hecogenone.
References
1. Marker, R . E . , Wagner, R . B . , Ulshafer, P. R . , Wittbecker, Ε . L . , Goldsmith, D . P. J . ,
and Rouf, C. H. (1943). J. Am. Chem. Soc. 65, 1199.
2. Callow, R . K . , Cornforth, J . W., and Spensley, P. C. (1951). Chem. Ind. (London) 699.
3. Gedeon, J . , and K i n d , F . A . (1953). Arch. Pharm. 286, 317.
Recommended Review
1. Stoll, Α . , and Jucker, E . (1955). Phytosterine, steroid saponine und herzglykoside. In
"Modern Methods of Plant Analysis," (K. Paech, and M. V. Tracey, eds.), Vol. 3, p. 141.
Springer-Verlag, New York.
5 4
F. Preparation of A -Cholesten-3-one and A -Cholesten-3-one
from Cholesterol
1. Introduction
Cholesterol dibromide has been prepared by unbuffered (1) and buffered (2)
bromination of cholesterol, and oxidized to 5a, 6/3-dibromocholestan-3-one
with acid permanganate (1), sodium dichromate (2), and chromic acid (3).
Debromination of 5,6-dibromocholestan-3-one with zinc dust in acetic
4
acid yielded A -cholesten-3-one (1), which is also formed by using sodium
iodide in refluxing benzene-ethanol (4). Butenand and Schmidt-Thome (3)
found that by using a neutral or weakly ionizing medium such as zinc in
5
boiling ethanol, A -cholesten-3-one is formed. The nonconjugated ketone is
4
easily isomerized to A -cholesten-3-one by a trace of mineral acid or alkali.
4
A -Cholesten-3-one has also been prepared by debromination of the
dibromoketone with ferrous chloride (5) or chromous chloride (6), by mod-
ification of the Windaus method (2), by Oppenauer oxidation of cholesterol
(7), and by catalytic dehydrogenation (8).
5 5
A -Cholesten-3-one has been prepared by oxidation of A -stenols
according to the Jones procedure ( 9 , 1 0 ) .
N a 2C r 20 7
Cholesterol
Cholesterol dibromide
/). 5-Cholesten-3-one /). -Cholesten-3-one
5a,6{3- Dibromocholestan-3- one
2. Principle
In the following procedure (11), the double bond of cholesterol is protected
by bromination, the dibromide is oxidized with sodium dichromate in acetic
acid, forming the dibromoketone, and debromination is accomplished with
4
ethanol-zinc dust. Isomerization to A -cholesten-3-one is effected by the
action of oxalic acid in hot ethanol.
3. Apparatus
Stirrer
II. Steroids 151
4. Materials
Acetic acid Ether, dry Sodium bicarbonate
Bromine Methanol Sodium dichromate
Cholesterol Oxalic acid Zinc dust
Ethanol Sodium acetate
5. Time
3 - 4 hours
6. Procedure
a. Cholesterol dibromide
Commercial cholesterol 15 g is dissolved in 100 ml absolute ether in a 500-ml
beaker by warming on the steam bath and stirring with a glass rod; the
solution is then cooled to 25°C. A second solution is prepared by adding 0.5 g
powdered anhydrous sodium acetate to 60 ml acetic acid, stirring the mixture,
and breaking up the lumps with a flat stirring rod; 6.8 g bromine is then
added, and the solution is poured, while stirring, into the cholesterol solution.
The solution turns yellow and promptly solidifies as a stiff paste of dibromide.
The mixture is cooled in an ice bath to 20°C, and the product is then collected
on a Büchner funnel. The cake is pressed and washed with acetic acid until
the filtrate is completely colorless; 50 ml is usually sufficient. Dibromide
moistened with acetic acid is satisfactory for most transformations; dry dibro-
mide, even when highly purified by repeated crystallization, begins to decom-
pose within a few weeks. When the material prepared as described is dried to
constant weight at room temperature, it is obtained as the 1:1 dibromide/
acetic acid complex; yield 17-18 g.
b. 5a, 6ß-Dibromocholestan-3-one
The moist dibromide obtained from 15 g cholesterol is suspended in 20 ml
acetic acid in a 500-ml round-bottomed flask equipped with a stirrer and
mounted over a bucket of ice and water. This ice bath can be raised to room
temperature (25-30°C). A solution (preheated to 90°C) of 8 g sodium dichro-
mate dihydrate in 200 ml acetic acid is introduced through a funnel. The
mixture reaches a temperature of 55 to 58°C during the oxidation, and all the
solid dissolves within 3 to 5 min. After an additional 2 min, the ice bucket is
raised until the flask is immersed. Stirring is then stopped, and the mixture is
allowed to stand in the ice bath for 10 min to allow the dibromoketone to
separate as readily filterable crystals. On resuming stirring, the temperature is
first brought to 25°C and then, after addition of 40 ml water, to 15°C. The
product is collected on a Büchner funnel, and the filter cake is drained until
the flow of filtrate amounts to no more than 25 drops per min. The suction is
released, the walls of the funnel are washed down with methanol, and 20 ml
methanol is added. After allowing the funnel to stand for a few minutes,
suction is again applied, and the crystals are drained thoroughly of solvent
before they are washed as described above with 20 ml fresh methanol. Dried
dibromoketone consists of shiny, white crystals, mp 73-75°C ( d e c ) ; yield,
about 17 g.
5
c. A -Cholesten-3-one
The moist 5a,6/3-dibromocholestan-3-one obtained from 15 g cholesterol is
transferred to a 500-ml round-bottomed flask and covered with 200 ml ether
and 2.5 ml acetic acid. The suspension is stirred mechanically, an ice bath is
raised into position, and the temperature is brought to 15°C. The ice bath is
then lowered, and 0.5 g fresh zinc dust is added. With the onset of the
exothermic reaction of debromination, the temperature is maintained at 15 to
20°C by cooling during the addition (in about 5 min) of 3.5 g zinc dust. The
ice bath is then lowered, and the ethereal solution containing suspended zinc
dust is stirred for an additional 10 min. With continued stirring, 4 ml pyridine
is added, bringing about the precipitation of a white zinc salt. The mixture is
filtered through a Büchner funnel, and the filter cake is washed well with
ether. The colorless filtrate is washed with three 60-ml portions of water and
then shaken thoroughly with 60 ml 5 % aqueous sodium bicarbonate solution
until free from acetic acid, as indicated by testing the ethereal solution with
moist, blue litmus paper. The solution is dried over magnesium sulfate and
evaporated to a volume of about 100 ml. Methanol (50 ml) is then added, and
the evaporation is continued until the volume is approximately 120 ml. Crys-
tallization is allowed to proceed at room temperature, then at 0 to 4°C. The
large colorless prisms are collected by suction filtration; yield, 8.7-9.4 g;
mp 124-129°C.
Concentration of the mother liquor gives a second batch of crystals
4
weighing 1.2-1.9 g, mp 117-125°C, and suitable for conversion to Δ -
cholesten-3-one. Total yield, 10.6-10.8 g.
5
d. IR spectrum of A -cholesten-3-one
- 1
(region 1300-1500 c m in C C 1 4 ; other regions in C S 2 )
- 1
1724 c m : C = 0 stretching, six-membered ring ketone
(nonconjugated)
1682: C = C , stretching, trisubstituted double bond
1436: unsubstituted C H 2 group in a six-membered ring adjacent to an
unsaturated bond
1377: angular methyl groups
1368: terminal gem-dimethyl group of side chain
960: out-of-plane bending of olefinic C—H bond
830: out-of-plane bending vibrations of H atom of a trisubstituted
olefin
II. Steroids 153
e. A -Cholesten-3-one
4
5
A mixture of 10 g A -cholesten-3-one, 1 g anhydrous oxalic acid and 80 ml
9 5 % ethanol is heated on a steam bath until all the solid has dissolved
(15 min) and heating is then continued for an additional 10 min. The solution
is then allowed to stand at room temperature. If crystallization has not started
after a period of several hours, the solution is seeded or the container is
scratched. After crystallization has proceeded at room temperature and then
at 0 to 4°C, the large, colorless, prismatic needles are collected by suction
filtration; yield, 9 g; mp 81-82°C.
4
f. A -Cholesten-3-one
13
h C NMR
C-l 35 7 C-10 38 6 C-19 17.4
C-2 33 9 C-ll 21 0 C-20 35.7
C-3 198 9 C-12 39 4 C-21 18.7
C-4 123 6 C-13 42 4 C-22 36.1
C-5 171 0 C-14 55 9 C-23 23.8
C-6 32 9 C-15 24 1 C-24 39.6
C-7 32 1 C-16 28 1 C-25 27.9
C-8 35 7 C-17 56 1 C-26 22.5
C-9 53 8 C-18 12 0
h. Mass spectrum
C 2 7 H 4 4 0 , Mol. wt. 384.
m/z 384(80%) 327(5%) 271(15%) 229(40%)
369(7%) 299(14%) 261(30%) 124(100%)
4
i. IR spectrum of A -cholesten-3-one
1 1
(region 1300-1800 c m " in C C 1 4 ; region 600-1300 c m " in C S 2 )
- 1
1672 c m . C = 0 stretching, α,/3-unsaturated in a six-membered ring
1620: C = C stretching, conjugated with carbonyl

1475: unperturbed side-chain C H 2 groups (in C 2 7 — C 2 9 steroids)
1438: unsubstituted C H 2 group in a six-membered ring adjacent to a
double bond
1425: free methylene at C 2
1378: methyl groups, angular
1368: terminal gem-dimethyl group of side chain
955: out-of-plane bending of olefinic C—H bond
866: vibration of a group composed of a carbonyl at C 3 conjugated
with C 4 = C 5
4
j. UV spectrum of A -cholesten-3-one
λ ™ 241 τημ (loge 4.25); 312 (2.00)

The peak at 241 ναμ is characteristic of a conjugated double bond system of
the type C = C — C = 0 . The peak at 312 π\μ is due to carbonyl absorption.
References
1. Windaus, A . (1906). Ber. 39, 518.
2. Fieser, L. F . (1953). J . Am. Chem. Soc. 75, 5421.
3. Butenand, Α . , and Schmidt-Thome, J . , (936). Ber. 69, 882.
4. Schoenheimer, R . (1935). J . Biol. Chem. 110, 461.
5. Bretschneider, H., and Ajtai, M. (1943). Monatsh. Chem. 74, 57.
6. Julian, P. L . , Cole, W . , Magnani, Α . , and Meyer, E . W . , (1945). J . Am. Chem. Soc. 67,
1728.
7. Oppenauer, R . V . , (1941). Org. Synth. 21, 18.
8. Kleiderer, E . C , and Kornfeld, E . C. (1948). J . Org. Chem. 13, 455.
9. Djerassi, C , Engle, R . R . , and Bowers, A . (1956). / . Org. Chem. 21, 1547.
10. Bowden, K . , Heilbron, I. M . , Jones, E . R . H., and Weedon, B . C. L. (1946). / . Chem. Soc.
39.
11. Fieser, L. F . (1963). Org. Synth. Coll. 4, 195.
Recommended Review
1. Fieser, L. F . , and Fieser, M. (1959). Investigation of Cholesterol. In "Steroids," p. 26.
Reinhold, New York.
G. Preparation of Vitamin D 2 and Its Separation by

Thin-Layer Chromatography
1. Introduction
The transformation of egosterol (provitamin D 2 ) to the corresponding vita-
min D begins immediately on exposure to ultraviolet light of suitable wave-
II. Steroids 155
length. This process occurs in overlapping stages, with the formation of a

series of products. The first stage is the photochemical conversion of ergos-
terol to pre-ergocalciferol, this reversible reaction providing yields of up to
8 5 % (1). The next stage is the thermal conversion of pre-ergocalciferol to
ergocalciferol (vitamin D 2 (2). During the irradiation, tachysterol 2 is formed
\
Ergosterol Ergocalciferol (Vitamin 02)
He~eat
CH3
Pre-ergocalciferol
Lumisterol Tachysterol
via a reversible photochemical side reaction of pre-ergocalciferol. Over-

irradiation of ergosterol yields biologically inactive products: toxisterol 2,
superasterol 2I, and suprasterol 2II (3). An isomer mixture rich in lumisterol
may be obtained by irradiating ergosterol with ultraviolet light of wavelength
exceeding 280 ιημ. It is noteworthy that irradiation of 7-dehydrocholesterol
gives rise to a series of products similar to those derived from ergosterol.
A vitamin D deficiency in humans leads to rickets.
2. Principle
In the following procedure (4) ergosterol is exposed to ultraviolet rays for a
few minutes, yielding tachysterol and vitamin D as the major irradiation
products. They are separated on thin layers of silica gel, and their ultraviolet
spectra are determined.
3. Apparatus
Spectrophotometer
TLC equipment
Ultraviolet lamp
4. Materials
Acetone Ether Skellysolve
Chloroform Potassium permanganate Sodium carbonate
Ergosterol Silica gel Sulfuric acid
Ethanol, 9 5 %
5. Time
2 - 3 hours
6. Procedure
a. Irradiation of ergosterol
Ergosterol 50 mg in 100 ml peroxide-free diethyl ether are placed in a 250-ml
round-bottomed quartz flask connected to a reflux condenser and exposed to
ultraviolet rays for 8 min. The solution is then stored at - 2 5 ° C under nitrogen
until such time as it is used for chromatographic analysis.
b. Preparation of plates
II. Steroids 157
gel and 50 ml water for 30 sec. It is then spread on the plates with an appli-
cator to give a layer of 0.25 mm thickness. The plates are activated at 160°C
overnight.
c. Development
A solution of 10 to 20 μg of the irradiation product in 2 μΐ either is applied to
the plate 2.5 cm from the bottom, and the plate is developed with 10%
acetone in Skellysolve (solvent 1), or with chloroform (solvent 2). When the
solvent has reached 10 cm above the starting line, the plate is removed from
the chamber and allowed to air-dry for 5 to 10 min.
d. Detection
The plates are sprayed either with 0.2% potassium permanganate in 1.0%
sodium carbonate solution or with 0.2 M sulfuric acid followed by heating at
140 to 150°C for 15 min.
e. Identification
The compounds separated are identified by the following technique: 1 to 2 mg
of the ergosterol irradiation mixture is streaked in a very narrow band across
the entire width of the plate at the origin. The separation is carried out as
described above. After drying, the plate is covered with a sheet of paper that
leaves 1-cm strips exposed at both edges. These are sprayed to locate the
bands of the separated compounds. Using the bands on the edges of the plate
as markers, strips of unsprayed silicic acid are scrapped off with a microscope
slide. The compounds are dissolved in acetone, and silicic acid is removed by
centrifugation or filtration. The acetone is evaporated with a stream of
nitrogen and replaced by 9 5 % ethanol, and the ultraviolet spectra of the
fractions are determined. The Rf values are summarized in the following
tables:
Identification of Compounds Identification of Mixtures
Rf in Solvent Rf in Solvent
Compound 1 2 Irradiation Mixture 1 2
Vitamin D 2 0.33 0.44 Spot I (tachysterol) 0.46 0.64

Vitamin D 3 0.32 0.44 Spot II (vitamin D 2 ) 0.33 0.44
Ergosterol 0.27 0.35 Spot III (ergosterol) 0.27 0.35
f. Vitamin D 2 (Calciferol)
1
g. H-NMR
Position of protons δ (ppm)
C 1 8( C H 3 ) 0.57
C 2 2( C H = C H ) 5.20
C 3( C H — O H ) 3.92
C6(=CH—CH=) 6.05
C7(=CH—CH=) 6.05
13
CNMR
C-l 32 00 C-ll 22.25 C-21 19.70
C-2 35 25 C-12 40.50 C-22 135.65
C-3 69 20 C-13 45.80 C-23 132.05
C-4 46 00 C-14 56.50 C-24 42.90
C-5 145 15 C-15 23.60 C-25 33.15
C-6 122 45 C-16 27.80 C-26 19.95
C-7 117 60 C-17 56.60 C-27 21.15
C-8 142 10 C-18 12.30 C-28 17.65
C-9 29 05 C-19 112.35
C-10 135 20 C-20 40.35
i. Mass Spectrum
Calciferol [Vitamin D 2 ] C 2 8 H 4 4 0 , Mol. wt. 396.
m/z 396(46%) 119(42%) 91(32%) 69(49%)
136(100%) 118(74%) 81(36%) 54(57%)
II. Steroids 159
j. IR spectrum of vitamin D 2 (in CCI4)

- 1
1645, 1628, 1602 c m : C = C stretching, triene (in chloroform)
1458: C H 2 bending
1374: C H 3 bending
1345: C—H bending
1050: C—Ο stretching of alcoholic OH
995-972: out-of-plane deformation of trans—CH=CH—group
(side-chain double bond C22-23)
k. UV spectrum of vitamin D 2
Η
λ ^ 265 τημ (loge 4.26)
The triene chromophore with its substituents gives rise to the absorption band
at 265 ιημ.
References
1. Velluz, L . , Amiard, G . , and Goffinet, B . (1955). Bull. Soc. Chim. France 1341.
2. Velluz, L . , Amiard, G . , and Pettit, A. (1949). Bull. Soc. Chim. France 501.
3. Windaus, Α . , Gaede, I . , Koser, J . , and Stein, G. (1930). Ann. 483, 17.
4. Norman, A . W., and DeLuca, H. F . (1963). Anal. Chem. 35, 1247.
Recommended Reviews
1. Bills, C. E . (1954). Vitamin D. In "The Vitamins" (W. H. Sebrell, and R . S. Harris eds.),
Vol. 2, p. 132. Academic Press, New York.
2. Jones, H., and Rasmusson, G . H. (1980). Recent advances in the biology and chemistry of
vitamin D . Prog. Chem. Org. Nat. Prod. 39, 63.
3. Velluz, L . , Amiard, G . , and Pettit, A . (1949). Bull. Soc. Chim. France 501.
4. Wagner, A . F . , and Folkers, K. (1964). The vitamin D group. In "Vitamins and Coen-
zymes," p. 330. Interscience, New York.
H. Determination of Sterols by Digitonin

I. Introduction
The ability of cholesterol to form a sparingly soluble complex with an equiva-
lent amount of digitonin was first noted by Windaus in 1910 [1]. Some
nonsteroid alcohols also form digitonides, but these differ in solubility and
stability from those of the sterols. Thus, the precipitation of a sterol with
digitonin is an effective method of isolation and purification of the sterols of
the 3/3-hydroxy series. Most of the commonly employed methods involving
digitonin precipitation of cholesterol or other 3/3-hydroxy sterols are lengthy,
in view of the time required for the quantitative precipitation of the sterol as
the digitonide complex. In 1937, Obermer and Milton (2) reported the use of
aluminum hydroxide as a gathering reagent for the rapid precipitation of
cholesterol digitonide. Brown, Zlatkis, Zak, and Boyle (3) have more re-
cently compared the use of aluminum hydroxide and aluminum chloride for
cholesterol digitonide precipitation from serum extracts, in combination with
the ferric chloride reagent (for color development).
2. Principle
The method described here (4) involves the rapid precipitation of 3ß-hydroxy
sterols, e.g., cholesterol, with digitonin and aluminum chloride in the pres-
ence of dilute hydrochloric acid.
The digitonides are then cleaved to their components with hot dimethyl
sulfoxide (5). When the solution is cooled to room temperature, the sterol
precipitates and is extracted with hexane. Recovery of sterol is almost quan-
titative, and the saponin is obtained by evaporation to dryness of the dimethyl
sulfoxide solution. The use of dimethyl sulfoxide has a distinct advantage of
convenience and speed of isolation of the digitonin-precipitable sterols.
3. Apparatus
Centrifuge
4. Materials
Acetone Dimethyl sulfoxide Hydrochloric acid
Aluminum chloride Ethanol Methanol
Cholesterol Ether, dry Pyridine
Digitonin
5. Time
3 - 4 hours
6. Procedure
a. Preparation of digitonides
Cholesterol (100 mg) is dissolved in 100 ml acetone-ethanol 1:1. 10 drops
3.5% hydrochloric acid (prepared by diluting 10 ml concentrated hydrochlo-
ric acid ( 3 5 % ) to 100 ml with distilled water), and 10 ml 0 . 5 % digitonin in
50% aqueous ethanol (prepared by dissolving 0.5 g digitonin in 100 ml 5 0 %
ethanol at 60°C) are mixed, and added to the above solution. Aluminum
chloride (10 ml, 1 0 % ) (100 g aluminum chloride hexahydrate dissolved in
distilled water and made up to 1 liter) is added, and the contents are mixed
and then heated at 45°C for 15 min. After cooling for 1 min, the tubes are
centrifuged for 20 min at 2500 rpm, the supernatant is decanted and dis-
carded, and the tubes are drained for 1 min by inversion. Methanol (20 ml) is
II. Steroids 161
then added to each tube, and the sterol digitonides are dissolved by gentle
warming. Hydrochloric acid (10 drops 3 . 5 % ) and 20 ml 10% aluminum
chloride are added and, following buzzing, the tubes are heated at 45°C for
20 min. The tubes are then cooled for 1 min, centrifuged at 2500 rpm for
20 min, decanted, and drained as in the previous step. To ensure complete
removal of digitonin, the methanol-aluminum chloride recrystallization step
is repeated. Finally, 20 ml acetone is added, and the precipitates are dis-
persed thoroughly by buzzing. They are centrifuged for 5 min at 2500 rpm,
and the solvent is decanted.
The digitonides are dissolved in 20 ml methanol and recrystallized by
addition of 2 ml 1 0 % aluminum chloride and heating at 45°C. Quantitative
recrystallization of cholesterol digitonides takes place after 15 min heating at
45°C. Complete purification is achieved by two such recrystallizations.
b. Cleavage of digitonides
The general procedure is illustrated by the following example. A mixture of
20 ml dimethyl sulfoxide and 1 g cholesteryl digitonide is heated on the steam
bath for 15 min, and the resulting solution allowed to cool to room tempera-
ture, whereupon cholesterol precipitates. The mixture is transferred to a
separatory funnel and extracted with 70 ml ra-hexane. The dimethyl sulfoxide
layer is extracted further with two 30-ml portions of n-hexane, and the
combined hydrocarbon layers are allowed to stand for 20 minutes over an-
hydrous sodium sulfate. Evaporation of the solvent leaves 0.22 g cholesterol
of mp 147-148°C. Evaporation of dimethyl sulfoxide to dryness, followed
by trituration of the residue with dry ether, gives 0.6-0.7 g digitonin.
References
1. Windaus, A . (1910). Z. Physiol. Chem. 65, 110.
2. Obermer, E . , and Milton, R . (1937). / . Lab. Clin. Med. 22, 943.
3. Brown, H. H., Zlatkis, Α . , Zak, B . , and Boyle, A . J . (1954). Anal. Chem. 26, 397.
4. Vahouny, G. V . , Borja, C. R . , Mayer, R . M., and Treadwell, C. R . (1960). Anal. Biochem.
1, 371.
5. Issidorides, C. H., Kitagawa, I . , and Mosettig, E . (1962). J. Org. Chem. 27, 4693.
6. Bergmann, W. (1940). / . Biol. Chem. 132, 471.
I. Gas—Liquid Chromatography of Steroids

1. Introduction
The application of gas chromatography to steroids has been restricted owing
to their low volatility. The first practical demonstration of the separation of
steroids was reported by Vanden Heuvel, Sweeley, and Horning (1). Before
the introduction of this method, Beerthuis and Recourt (2) and others had
chromatographed steroids at high temperatures on silicone oil.
A variety of liquid phases have been exploited for gas chromatography

of steroids: fluorinated silicone ( 3 ) , neopentyl glycol succinate ( 4 ) , nitrile
silicone (5), polydiethylene glycol succinate (6), and many others. Many
derivatives of steroids have been prepared in order to increase their volatility,
decrease the adsorption on the column, and prevent thermal breakdown. The
polarity of hydroxylated steroids can be reduced by preparation of O-methyl
ethers ( 6 , 7 ) , acetates ( 8 , 9 ) , trifluoroacetates (10), or trimethylsilyl ethers
(11).
Considerable progress has been made in the studies of correlating the
retention time of steroids with their structure. Apparently, it will be possible
to predict a number of structural characteristics of a given steroid from its
retention time data (12).
2. Principle
It is important that the support material should be inert with regard to the
sample component. If this is not the case, interactions with the samples will
take place, leading to asymmetrical peaks and partial loss of the injected
amounts due to irreversible adsorption or decomposition.
In gas chromatography, diatomaceous earth-type support materials are
generally used. They have the following active groups at their surface:
—Si — Si— and — Si—O—Si—
When polar substances such as steroids are analyzed, they will interact
strongly with these active groups. The blocking of these groups is achieved by
silanization of the support before coating, e.g., by treatment with dichloro-
dimethylsilane or hexamethyldisilazane. In both cases, the free OH groups
become chemically bonded:
Si —Si—Si—
A or Ο Ο
\ /
C H 3— S i — C H 3 Si
CH3 CH3 CH3
The reaction of a steroid with equivalent amounts of trimethylchlorosi-
lane and hexamethyldisilazane proceeds according to the following equation:
3 R O H + (CH 3 ) 3 SiCl + (CH3) 3SiNSi(CH 3)3 * 3 R O S i ( C H 3) 3 + NH 4C1
This silanization considerably reduces the support activity (13).
II. Steroids 163
The ease of preparation and the excellent G L C properties are the

reasons for the widespread use of trimethylsilyl ethers of steroids in G L C
analysis.
In the following procedure (1,14) the support and column are silanized
with dichlorodimethylsilane, and the sterols are analyzed as methyl ethers,
acetates, keto-derivatives, or trimethylsilyl ethers.
Apparatus
Gas Chromatograph
Materials
Androstane Cholesteryl acetate
Androstane-17-one Chromosorb W (80-100 mesh)
Androstane-3,17-dione Coprostane
Cholestane Dichlorodimethylsilane
Cholestanyl methyl ether Gas Chrom Ρ or Q
Cholesteryl methyl ether Hexamethyldisilazane
Cholestan-3-one Silicone gum, S E - 3 0
4-Cholesten-3-one ^-Sitosterol
Cholestanol β-Sitosteryl acetate
Cholesterol Stigmastane
Cholestanyl acetate Stigmasterol
Time
3 hours
Procedure
Preparation of columns
A glass column 6 ft in length and 4 mm in diameter is used. The support is
acid-washed Chromosorb W, inactivated by treatment with dichlorodimethyl-
silane. Inactivation is carried out by placing 20 g support in 80 ml 5 % dichlo-
rodimethylsilane in toluene in a round-bottomed flask fitted with a side arm.
The flask is brought under reduced pressure, and the mixture is swirled for a
few minutes to dislodge air bubbles from the surface of the support. After
10 min, the support is removed by filtration and washed with 100 ml toluene.
The support is then washed well with methanol by resuspension in this solvent
and dried for 2 hr at 80°C. It is then suspended in 100 ml 2 % S E - 3 0 in
toluene, and a gentle vacuum is applied for 15 min to remove occluded air.
The suspension is then poured in one lot onto a Büchner funnel, applying
gentle suction, which is released as soon as the bulk of the solution has been
filtered. The moist support is transferred to a filter paper and is dried in air
and finally in an oven at 80°C.
Glass columns and glass wool for packing are treated with 5%
dichlorodimethylsilane in toluene, washed with toluene and methanol, and
dried. Columns are packed by gradual addition of the coated support and
repeated tapping. The freshly packed column is heated to 300°C in a slow
stream of argon or helium for 12 hr to remove volatile products.
b. Preparation of samples
The steroids are dissolved in analytical grade chloroform or tetrahydrofuran
at a concentration of about 2 mg/ml, and suitable portions are mixed with
cholestane for chromatography. The quantity of steroid to be injected is
0.1-1.0 /xg.
c. Operating conditions
Standard conditions are column temperature, 222°C; injector maintained at
50°C above column temperature; detector, 240°C; argon flow rate, 30 ml/min
at outlet; inlet pressure, 10-15 psi. The following table summarizes the reten-
tion data relative to cholestane. The retention time of cholestane is 17.6
minutes.
Retention Data of Steroids
Compound Relative Retention Time
Androstane 0.11
Androstan-17-one 0.22
Androstan-3,17-dione 0.47
Coprostane 0.90
Cholestane 1.00
Cholestanyl methyl ether 1.78
Cholesteryl methyl ether 1.72
Cholestan-3-one 2.17
4-Cholesten-3-one 2.72
Cholestanol 1.99
Cholesterol 1.98
Cholestanyl acetate 2.84
Cholesteryl acetate 2.81
j8-Sitosterol 3.26
/3-Sitosteryl acetate 4.62
Stigmastane 1.65
Stigmasterol 2.84
Sterols may also be analyzed as trimethylsilyl ethers, which can be

prepared by dissolving 25 mg free sterol in 1 ml anhydrous tetrahydrofuran in
a small glass-stoppered test tube. Hexamethyldisilazane (0.5 ml) and 10 μ\
trimethylchlorosilane are added, and the tube is tightly stoppered and heated
for 30 min at 55°C. The cooled mixture may be injected directly into a glass or
II. Steroids 165
stainless steel column filled with Gas Chrom Q (silanized Gas Chrom Ρ)
impregnated with 1 to 2 % S E - 3 0 . The experimental conditions are similar to
those outlined above.
References
1. Vanden Heuvel, W. J . Α . , Sweeley, C. C , and Horning, E . C. (1960). J. Am. Chem. Soc.
82, 3481.
2. Beerthuis, R . K . , and Recourt, J . H. (1960). Nature (London) 186, 372.
3. Vanden Heuvel, W. J . Α . , Haahti, Ε . Ο. Α . , and Horning, E . C. (1961). / . Am. Chem.
Soc. 83, 1513.
4. Haahti, Ε . Ο. Α . , Vanden Heuvel, W. J . A. and Horning, E . C. (1961). / . Org. Chem.
26, 626.
5. Vanden Heuvel, W. J . Α . , Creech, B . G . , and Horning, E . C. (1962). Anal. Biochem.
4, 191.
6. Clayton, R . B . (1962). Biochemistry 1, 357.
7. Knights, B . A . (1964). J. Gas Chromatogr. 160.
8. Wotiz, Η. H., and Martin, H. F . (1961). J. Biol. Chem. 236, 1312.
9. Nishioka, I . , Ikekawa, N., Yagi, Α . , Kawasaki, T . , and Tsukamoto, T . (1965). Chem.
Pharm. Bull. (Japan) 13, 379.
10. Vanden Heuvel, W. J . Α . , Sjovall, J . , and Horning, E . C. (1961). Biochim. Biophys. Acta
48, 596.
11. Luukkainen, T . , Vanden Heuvel, W. J . Α . , Haahti, Ε . Ο. Α . , and Horning, E . C. (1961).
Biochim. Biophys. Acta 52, 599.
12. Vanden Heuvel, W. J . Α . , and Horning, E . C. (1962). Biochim. Biophys. Acta 64, 416.
13. Kabot, F . J . , and Ettre, L. S. (1963). "Gas chromatographic analysis of steroids." The
Perkin-Elmer Corporation, Norwalk, Conn.
14. Brooks, C. J . W . , and Hanaineh, L . (1963). Biochem. J. 87, 151.
Recommended Reviews
1. Horning, E . C , Vanden Heuvel, W. J . Α . , and Creech, B . G. (1963). Separation and
determination of steroids by gas chromatography. In "Methods of Biochemical Analysis," ( D .
Glick, ed.), Vol. 11, p. 69. Interscience, New York.
2. Kuksis, A . (1966). Newer developments in determination of bile acids and steroids by gas
chromatography. In "Methods of Biochemical Analysis." ( D . Glick, ed.), Vol. 14, p. 325.
Interscience, New York.
J. Thin-Layer Chromatography of Sterols and Stanols on Silica

Impregnated with Silver Nitrate
1. Introduction
Sterols such as cholesterol and ß-sitosterol occur very often in natural sources
as inseparable mixtures with the corresponding stanols. Ikan and Kashman
(1) have found a mixture of ß-sitosterol and /3-sitostanol in Israeli peat.
Similar observations have been made by McLean, Rettie, and Spring (2) on
Scottish peat, and by Ives and O'Neill (3) on Canadian peat moss. It has been
shown that by bromination of such critical pairs, the unchanged stanols are
easily separated on thin layers from the brominated sterols. This may be
accomplished either by spotting bromine in carbon tetrachloride over the
mixture at the start line ( 4 , 5 ) , or by incorporating bromine in the mobile
phase (6).
In 1937, Lucas and his coworkers (7) showed that the coordination of
silver ions with unsaturated compounds is rapid and reversible. This principle
has been applied by Morris (8) to cholesteryl esters, by Avigan, Goodman,
and Steinberg (9) to sterols and steroids, and by Ikan (10) to tetracyclic
triterpenes. All these workers used thin layers of silica gel impregnated with
silver nitrate.
2. Principle
The following method is according to Ikan and Cudzinovski (11).
3. Apparatus
TLC applicator
4. Materials
Acetic acid Chlorosulfonic acid Silver nitrate
Campesterol Coprostanol /3-Sitosterol
Campestanol Ergosterol ß-Sitostanol
Chloroform Methanol Stigmasterol
Cholesterol Phosphomolybdic acid Sulfuric acid
Cholestanol Silica gel G
5. Time
3 hours
6. Procedure
The suspension for 5 plates (20 x 20 cm) is prepared by shaking 30 g silica gel
G and 60 ml water for 30 sec. It is applied uniformly to a thickness of 0.25 mm
with an applicator. After 30 min at room temperature, the plates are heated
in an oven an 125 to 130°C for 45 min. After cooling, they are sprayed with
concentrated aqueous methanolic silver nitrate solution, 5 % relative to silica
gel, and then activated at 120°C for 30 min. This method permits impregna-
tion of only part of the plate, which can thus be used for comparative
chromatography.
II. Steroids 167
b. Development
The samples are dissolved in chloroform (1 mg/ml) and applied with micro-
pipettes along a line 2 cm above the rim of the plate. Chloroform is used as
the mobile phase; it is allowed to travel over a distance of 15 cm. The plates
are then removed and dried in air.
c. Spray reagents
1. 5 0 % sulfuric acid in water
2. 1 0 % phosphomolybdic acid in ethanol
3. a mixture of chlorosulfonic and acetic acids, 1:1
The steroids are detected by spraying one of the three mentioned
reagents, followed by heating in an oven at 150°C for 15 min. The colors of
the spots are recorded before and after charring.
The following sterols are tested: campesterol, campestanol, chole-
sterol, cholestanol, coprostanol, ergosterol, /3-sitosterol, β-sitostanol, and
stigmasterol.
References
1. Ikan, R . , and Kashman, J . (1963). Israel J. Chem. 1, 502.
2. McLean, J . , Rettie, G. H., and Spring, F . S. (1958). Chem. Ind. {London), 1515.
3. Ives, D . A . J . , and O'Neill, A . N. (1958). Can. J. Chem. 3 6 , 436.
4. Cargill, D . I. (1962). Analyst 87, 865.
5. Ikan, R . , Harel, S., Kashman, J . , and Bergmann, E . D. (1964). J. Chromatogr. 14, 504.
6. Copius Peereboom, J . W., and Beekes, H. W. (1962). J. Chromatogr. 9, 316.
7. Alberz, W. F . , Welge, H. J . , Yost, D . M., and Lucas, H. J . (1937). J. Am. Chem. Soc.
59, 45.
8. Morris, L . J . (1963). / . Lipid Res. 4, 357.
9. Avigan, J . , Goodman, de W. S., and Steinberg, D . (1963). / . Lipid Res. 4, 100.
10. Ikan, R . (1965). J. Chromatogr. 17, 591.
11. Ikan, R . , and Cudzinovski, M. (1965). J. Chromatogr. 18, 422.
Recommended Review
1. Morris, L. J . (1964). Specific separations by chromatography on impregnated adsorbents. In
"New Biochemical Separations" A . T. James, and L. J . Morris, (eds.) p. 294. Van Nostrand,
Princeton, NJ.
K. Questions
1. What are sterols? Write the structure for cholesterol and number the
positions in the rings.
2. Point out the structural similarities and differences between the male
and female sex hormones.
3. Distinguish between hormones, enzymes, and vitamins.

4. Indicate a natural source of stigmasterol, vitamin D , and
corticosterone.
5. Why is ergosterol called provitamin D ?
6. What are the "orange juice vitamin" and the "sunshine vitamin"?
7. What are marine sterols?
8. Describe the biosynthesis of cholesterol and stigmasterol.
9. What are saponins? Give examples and describe applications.
L. Recommended Books
1. Cook R. P. (1958). "Cholesterol" Academic Press, New York.

2. Fieser, L. F . , and Fieser, M. (1959). "Steroids" Reinhold, New York.
3. Klyne, W. (1957). "The Chemistry of Steroids " John Wiley, New
York.
4. Kritchevsky, D . (1958). "Cholesterol" John Wiley, New York.
5. Richards, J . H., and Hendrickson, J . B . (1964). "The Biosynthesis of
Steroids, Terpenes, and Acetogenins ." Benjamin, W. A.
6. Shoppee, C. W. (1958). "Chemistry of the Steroids " Academic Press,
New York.
III. TERPENOIDS
A. Introduction
Terpenoids are widely distributed in nature, mostly in the plant kingdom.

They may be regarded as derivatives of oligomers of isoprene,
C H 2 = C — C H = C H 2 , usually joined head to tail. Terpene hydrocarbons
CH2
are classified as follows:
Monoterpenes, C 1 0H 1 6
Sesquiterpenes, C 1 5H 2 4
Diterpenes, C 2 0H 3 2
Triterpenes, C 3 0H 4 8
Tetraterpenes, C 4 0H 6 4
Polyterpenes, ( C 5H 8) „
Abundant sources of terpenoids are the essential oils. They consist of a

complex mixture of terpenes or sesquiterpenes, alcohols, aldehydes, ketones,
acids, and esters. There are four general methods for the extraction of
essential oils: (1) expression; (2) steam distillation; (3) extraction with volatile
solvents; (4) resorption in purified fats. The separation of individual compo-
III. Terpenoids 169
nents is accomplished by vacuum fractionation and by chromatographic

methods. The unsaturated hydrocarbons are conveniently separated as their
crystalline addition products with hydrochloric acid, hydrobromic acid, or
nitrosyl chloride.
1. Monoterpenes
The monoterpenes are subdivided into three groups: acyclic, monocyclic, and
bicyclic.
a. Acyclic monoterpenes
Among the important hydrocarbons are ocimene and myrcene.
CH,
CH2
H 3C CH2 H3C CHq

Ocimene Myrcene
Aldehydes
CHO
H 3C CH3
Geranial
Alcohols
CH, CH
CH,OH
H 3C CH3 H,C CH, H,C CH,

Geraniol Nerol Linalool
Numerous examples of the cyclization of acyclic monoterpenes to alicy-

clic or aromatic compounds are known, e.g., the conversion of citral to a- and
ß-cyclocitral.
H 3C CH H 3C CH3 H
n 33 C
^ C H 33
v_n
CHO +
CHO X ^CHO
H
+
CH, CH, CH3
Citral a-Cyclocitral /i-Cyclocilral
b. Monocyclic monoterpenes
Important hydrocarbons are:
CH CH,
H,C H,C^ "CH H 3C ^ ^CH3

a-Terpinene ß-Terpinene
CH,
H,(T ΧΉ, H3C^ ^CH3 H 3 C " "CH

y-Terpinene a-Phellandrene ß-Phellandrene
CH CH
OH
OH OH
H 3C ^ ^CH3 H3C" "CH3 H3C CH3 H 3C CH2

Menthol Piperitol Carveol
III. Terpenoids 171
Aldehydes
CHO CHO
Perillaldehyde Phellandral
Ketones
Menthone Pulegone Piperitone Carvone
Oxides
1,8-Cineole Ascaridole
c. Bicyclic monoterpenes
The bicyclic monoterpenes may be divided into five groups.
Thujane group
α-Thujene Sabonene Thujone Sabinol

Carane group
Car-3-ene Car-4-ene Carone
Pinane group
a-Pinene β-Pinene Myrtenal Myrtenol
Camphane group
Camphor Borneol Camphene
Fenchane group
Fenchone Fenchyl alcohol a-Fenchene
2. Sesquiterpenes
The sesquiterpenes form the higher-boiling fraction of the essential oils. They
are formed by the union of three isoprene units. Sesquiterpenes are unsatu-
rated compounds and may be acyclic, monocyclic, bicyclic, and tricyclic.
II. Terpenoids 173
a. Acyclic sesquiterpenes
H,<X ^CH
CH,
CH,OH
Farnesol
Farnesol
Farnesol Nerolidol
b. Monocyclic sesquiterpenes
Cl- Bisabolene Zingiberene
c. Bicyclic sesquiterpenes
p-SeJinene
Cadalene
α-Cyperone Santonin
d. Azulenes
Many essential oils have a blue or violet color, or may take on such colors
after dehydrogenation with sulfur, selenium, or palladium.
CH
H 3C
Azulene
Vetivazulene
CH,
Guaiazulene
CH2
CH3
CH3
H 3C CH3
ß-Vetivone
Aromadendrene
CH
CH,
H,C
Linderazulene
Some sesquiterpenes show greater structural complexity, e.g., caryophyllene.
H 3C
CH,
H,C
H 2C
Caryophyllene
3. Diterpenes
The diterpenes are formed by the union of four isoprene units and are found
mainly in the resins of plants.
III. Terpenoids 175
a. Acyclic diterpene
C H 3— C H — ( C H 2) 3C H — ( C H 2) 3C H — ( C H 2) 3C = C H — C H 2O H
CH3 CH3 CH3 CH3
Phytol
b. Monocyclic diterpene
Vitamin Ai
c. Bicyclic diterpenes
CH3 OH
Sclareol Manool
d. Tricyclic diterpenes
The resin acids form the major nonvolatile part of many natural resins,
especially those of coniferous trees.
Abietic acid Levopimaric acid

Podocarpic acid Ferruginol
4. Triterpenes
The triterpenes are widely distributed in the plant and animal kingdoms,
where they occur either in the free state, as esters, or as glycosides. They may
be classified into three groups: (1) acyclic; (2) tetracyclic; (3) pentacyclic.
Many conversions from one group to another have been accomplished.
Some of the transformations involved the change of a — C O O H to the
corresponding — C H 3 or to C H 2 O H .
RCOOH > RCOC1 • RCHO > RCH3

i
R C H 2O H • RCHO > RCH3
i
R C H 2O T s • RCH3
An important reaction is the detection of a gem-dimethyl group at the

C 4 position.
Terpenoids 177
CH, CH,
PCI 5
H
H 3C CH3 H 3C CH3 H 3C CH
CH
H,C
CH,
Valuable information on the carbon skeletons of triterpenoids can be

obtained by dehydrogenation, which yields the following products:
CH,
CH,
CH, H 3C CH3 H 3C CH,

CH, CH3
3 2,7-Dimethylnaphthalene
1,2,3,4-Tetramethylbenzene 1,2,7-Trimethylnaphthalene
CH3 CH3 CH,

CH, CH, CH,
' J
Η 3 σ ^ γ ^ ^ HO
CH3
CH3 CH3
1,2,5,6- Tetramethylnaphthalene l,5,6-Trimethyl-2-naphthol 1,5,6-Trimethylnaphthalene
CH3 CH,
HO
CH, CH,
1,8-Dimethylpicene 2-Hydroxy-l,8-dimethylpicene
The main dehydrogenation product of tetracyclic triterpenes is
CH3
l ,2,8-Trimethylphenanthrene
a. Acyclic triterpenes
Squalene Ambrein
b. Tetracyclic triterpenes
Cyclolaudinol
III. Terpenoids 179
c. Pentacyclic triterpenes
These compounds are subdivided into three groups based on established
interrelationships with one of three standards, α-amyrin, /3-amyrin, and
lupeol.
α-Amyrin group
α-Amyrin Ursolic acid
Asiatic acid
/3-Amyrin group
/?-Amyrin Oleanolic acid

Glycyrrhetic acid
Lupeol group
Taraxasterol
It is important to note that squalene and lanosterol-like products are

intermediates in the biosynthesis of cholesterol.
III. Terpenoids 181
H3 C CH 3
~
H3 C CH 3
CH 3
H3 C CH 3
Squalene
CH 3
--( ~
CH 3
HO
H3C Lanosterol
CH 3
----»
CH 3
HO I
H
CH 3
~
H3 C CH 3
HO
Desmosterol
CH 3
H 3C
CH 3
HO
Cholesterol
Β. Conversion of D-Limonene to L-Carvone and Carvacrol

1. Introduction
The terpene hydrocarbon, D-limonene, is the major constituent of all citrus
peel oils. Sweet orange contains about 9 5 % D-limonene, 1-2% n-octanal and
n-decanal, 0 . 0 5 - 1 . 5 % n-nonanal and D-linalool, and traces of other hydrocar-
bons, carbonyl compounds, alcohols, esters, and acids. Bernhard (1) applied
gas-partition chromatography to the examination of lemon oil and identified
about 30 constituents.
D-Limonene is structurally related to L-carvone and can be converted
into it via the sequence of reactions outlined below. The conversion of
NO
H 3C
D-Limonene Limonene nitrosochloride
DMF
CH3
NOH
Carvoxime
CH3 CH3
OH
H 3C CH3 H 3CT ^ C H 2
Carvacrol L-Carvone
III. Terpenoids 183
D-limonene to the nitrosochloride has been effected by the action of gaseous

nitrosyl chloride ( 2 ) , ethyl nitrite ( 3 ) , amyl nitrite ( 4 ) , and nitrogen trioxide
(5). Dehydrohalogenation was effected by the following reagents: alcohol ( 6 ) ,
alcoholic solutions of sodium hydroxide and potassium hydroxide (7), sodium
methylate ( 8 ) , and pyridine ( 3 , 9 ) . Hydrolysis of L-carvoxime to L-carvone
without racemization or isomerization is readily effected by refluxing with 5 %
aqueous oxalic acid. The use of dilute (5N) mineral acids leads to the
formation of carvacrol as the major hydrolysis product.
2. Principle
According to the following method ( 1 0 , 1 1 ) , limonene nitrosochloride is

formed in situ by simultaneous addition of sodium nitrite and hydrochloric
acid to limonene. It is then converted into carvoxime by boiling with
dimethylformamide. Hydrolysis of L-carvoxime to L-carvone is effected with
hot oxalic acid. In order to minimize the time of contact of carvoxime and
carvone with the acidic media, carvone is removed from the reaction mixture
by steam distillation as rapidly as it is formed.
Treatment of carvoxime with mineral acid leads to the formation of
carvacrol, which may be characterized through the formation of 2-methyl-5-
isopropylphenoxy-acetic acid.
3. Apparatus
Stirrer
4. Materials
Chloroform Isopropanol
Chloroacetic acid Methanol
Dimethylformamide Oxalic acid
2,4-Dinitrophenylhydrazine Semicarbazide hydrochloride
Essential oil of oranges Sodium carbonate
Ether Sodium hydroxide
Hydrochloric acid Sodium nitrite
5. Time
5 - 6 hours
6. Procedure
a. Isolation of D-limonene from the essential oil of oranges

Crude essential oil of oranges (100 g) is fractionally distilled under reduced
pressure. D-Limonene distills at 75°C/27 mm as a colorless oil weighing 75 g.
b. NMR spectrum of limonene
Position δ (ppm)
a 1.64
b 1.72
c 1.97
d 4.66
e 5.35
c. Limonene nitrosochloride
A solution of 40.8 g D-limonene in 40 ml isopropanol is cooled below 10°C.
To this solution are added simultaneously, through separate dropping fun-
nels, a solution of 120 ml concentrated hydrochloric acid in 80 ml isopropanol
and a concentrated aqueous solution of 20.7 g sodium nitrite. The addition is
controlled so as to maintain the temperature below 10°C. The mixture is
stirred for an additional 15 min and is allowed to stand in a refrigerator for
1 hr. The solid is filtered on a Büchner funnel and washed with cold ethanol;
yield 50 g. It is crystallized from a mixture of chloroform-methanol, 1:3;
mp 103°C.
d. Carvoxime
Limonene nitrosochloride (40 g) (crude product is permissible) and 20 ml
dimethylformamide are boiled for 30 min under reflux in 125 ml isopropanol.
The solution is then poured into 500 ml cracked ice and water, stirred vigor-
ously, and filtered after the ice has melted. The solid is washed three times
with 50 ml cold water and once with 15 ml cold isopropanol. The dry product
weighs 27 g; mp 66-69°C. If the product is an oil, it is extracted with di-
chloromethane, which is then evaporated.
e. L-Carvone
A mixture of 10 g L-carvoxime and 100 ml 5 % aqueous oxalic acid is refluxed
for 2 hr. At the end of this period, the reaction mixture is steam distilled, and
the distillate is extracted with ether. The ethereal solution is dried over
sodium sulfate and fractionally distilled to give 7 g L-carvone, bp 88-90°C at
4 mm. Semicarbazone is prepared in methanol; it melts at 162°C. 2,4-
Dinitrophenylhydrazone melts at 189°C.
III. Terpenoids 185
f. Carvone
1
g. H NMR
δ Η 1.76(6H, 2 x C H 3 ) 4.79(2H, C = C H 2 )
2.00-2.90(5H, 2 x C H 2 , CH) 6.74(1H , C = C H )
13
C NMR
C-l δ 15.4 C-6 43.1
C-2 135.2 C-7 197.7
C-3 143.8 C-8 147.2
C-4 31.3 C-9 20.2
C-5 42.7 C-10 110.3
Mass spectrum
Carvone, C i 0 H i 4 O , Mol. wt. 150
m/z 150(1%) 82(100%) 54(67%) 41(32%)
108(18%) 79(14%) 53(23%) 39(58%)
93(25%)
IR spectrum of carvone (sandwich cell)

1
3320 c m " : overtone of C = 0
2955, 2865: stretching of C H 3
1675: C = 0 stretching, α,/3-unsaturated
1645: C = C stretching of terminal methylene
1450: C H 2 scissor
1435, 1370: C H 2 and C H 3 bending
1055: aliphatic ketone
890: out-of-plane bending of terminal methylene
802: out-of-plane bending of trisubstituted double bond
UV
\ EtOH
235 νημ (loge 3.93); 318(1.62)
The 235 ιημ peak is characteristic of a conjugated double bond system

of the type C = C — C = 0 .
The 318 πιμ peak is due to the excitation of one of the lone pair electrons of
the oxygen (carbonyl absorption). Note its lower intensity.
I. Carvacrol
A mixture of 10 g L-carvoxime and 50 ml 5N hydrochloric acid is refluxed for
15 min. The mixture is steam distilled, the distillate is extracted with ether,
and the ethereal solution is dried over anhydrous sodium sulfate. Removal of
the ether leaves 6.5 g oil (which is soluble in 5 % aqueous sodium hydroxide).
The oil is characterized as carvacrol through the formation of 2-methyl-
5-isopropylphenoxyacetic acid (mp 152°C) which is prepared as follows: to a
mixture of 1 g of the phenol and 3.5 ml 3 3 % sodium hydroxide solution is
added 2.5 ml 5 0 % chloroacetic acid solution; if necessary, a little water is
added to dissolve the sodium salt of the phenol. The test tube containing the
solution is stoppered loosely and heated for 1 hr in a gently boiling water
bath. The solution is cooled, diluted, acidified to Congo red with a mineral
acid, and extracted once with ether. The ether extract is washed once with a
little water, and the aryloxyacetic acid is removed by washing with dilute
sodium carbonate. Acidification of this extract gives the free acid, which is
recrystallized from water.
m. Thin-layer chromatography of carvone and carvacrol

A drop each of carvone and carvacrol ( 5 % in chloroform) is spotted on a
thin-layer plate (Silica Gel G F 2 5 )4 and developed with chloroform-benzene
3:1.
Detection: (1) UV254—dark spots. (2) Spraying with phosphomolybdic
acid reagent, prepared by dissolving phosphomolybdic acid (20 g) in ethanol
(100 g). After heating at 110°C for 10 min, blue spots on a yellow background
are observed. Carvone, R{ 0.55.
References
1. Bernhard, R . A . (1958). / . Food Res. 23, 213.
2. Tilden, W. Α . , and Shenstone, W. A. (1877). J . Chem. Soc. 3 1 , 554.
3. Royals, Ε . E . , and H o m e , S. E . (1951). / . Am. Chem. Soc. 73, 5856.
4. Wallach, Ο. (1889). Ann. 252, 109.
5. Rupe, H. (1921). Helv. Chim. Acta. 4, 149.
6. Goldschmidt, Η., and Zurrer, R . (1885). Ber. 18, 2220.
7. Wallach, Ο. (1892). Ann. 270, 175.
8. Deussen, Ε . , and Hahn, Α. (1909). Ann. 369, 60.
9. Wallach, Ο. (1918). Ann. 414, 257.
10. Reitsema, R . H. (1958). J . Org. Chem. 23, 2038.
II. Earl, Ε . E . , and Hörne, S. E . (1951). / . Am. Chem. Soc. 73, 5856.
Recommended Reviews
1. Guenther, E . (1949). Essential oils of the genus Citrus. In "The Essential Oils" Vol. 3, p. 5.
Van Nostrand, New York.
III. Terpenoids 187
2. Kefford, J . F . (1959). The chemical constituents of citrus fruits. In "Advances in Food

Research." (C. O. Chichester, Ε . M. Mrak, and G . F . Stewart, eds.), Vol. 9, p. 286.
3. Kirchner, J . G . (1961). Oils of peel, juice sac, and seed. In "The Orange" (W. B . Sinclair,
ed.), p. 265. University of California Press, Berkeley, California.
4. Shaw, P. E . , and Wilson, C. W. (1980). Importance of selected volatile components to
natural orange, grapefruit, tangerine, and mandarin flavors. In "Citrus Nutrition and Qual-
ity." (S. Nagy, and J . A . Attaway, eds.), p. 167, A C S Symposium Series 143.
C. Isolation and Determination of Optically Pure Carvone

Enantiomers from Caraway (Carum carvi L.) and Spearmint
(Mentha spicata L.)
( R ) - ( - ) - c a r v o n e (spearmint) (S)-( + )-carvone (caraway)
1. Introduction
Optical purity of enantiomers is of great importance in the chemistry of
natural products, especially in the fields of flavors, fragrances, and pher-
omones. Odor receptors in mammals and in insects can discriminate between
enantiomers, so it is important to describe the enantiomeric composition of
chiral molecules that impinge on these receptors.
The human olfactory organ is capable of distinguishing between chiral
compounds. Odor quality and potency of enantiomeric compounds may show
considerable differences. Thus, a distinct differentiation in odor perception
could be observed in pairs of enantiomeric monoterpenoid and sesquiterpe-
noid odorants. The intensity of the odor of enantiomeric compounds exhibits
as great a variability as does the quality. In theory, chiral receptor sites should
acknowledge the spatial arrangements of enantiomers; careful experiments
have shown that some insects are capable of making the distinction.
Methods for the determination of enantiomeric composition are as
follows:
1. Polarimetry;
2.
1 1 3
NMR ( H and C ) : chiral shift reagent; chiral derivatizing agent;
chiral solvating agent;
3. Achiral chromatography (GC or HPLC): separation of diasteriomeric
derivatives;
4. Chiral chromatography (GC or HPLC): separation of enantiomers;

and
5. X-ray crystallography of a diasteriomeric derivative.
The classical procedure for determination of enantiomeric composition
(or optical purity) is polarimetry. The basic requirements are a relatively
large sample, a relatively high specific rotation, and a knowledge of the
specific rotation of the pure enantiomer under similar conditions. High-per-
formance methods of enantiomer analysis are urgently needed in order to
keep pace with the development of highly enantioselective reactions and to
cope with the requirements of mechanistic investigations.
The simple and effective method for determination of enantiomeric
composition is NMR-polarimetry—NMR spectroscopy using chiral Lan-
thanide shift reagents ( L S R ) . L S R are the europium and praseodym salts of
/3-diketones:
Ln = E u E u ( t f c ) 3 Eu(dcm)3 Ln = E u Eu(hfc)3
Ln = Pr Pr(tfc) 3 Ln = Pr Pr(hfc) 3
These chiral L S R are used to determine the enantiomeric purity of

optically active compounds ( 1 ) . L S R interacts diastereomerically with a pair
of enantiomers forming a chelate; this leads to separated NMR signals for
corresponding nuclei in the two enantiomers. Europium chelates generally
cause downfield shifts, whereas the praseodym analogues effect upfield shifts.
The L S R reagents induce a considerable spread of the chemical shifts without
significantly broadening the lines (2). The method is applicable to a much
broader range of compounds than some of the other techniques.
McCreary and colleagues (3) reported the first use of chiral L S R with
[
H-NMR spectrometry to determine the enantiomeric composition of the
monoterpenes camphor, menthol, and menthyl acetate. Plummer and associ-
ates (4) and Borden and colleagues (5) determined the enantiomeric purity of
several pheromones, including the monoterpene alcohols rrans-verbenol,
ipsdienol and sulcatol using a chiral shift reagent. In the following experiment
the determination of the enantiomeric composition of natural carvones iso-
lated from various essential oils, using a chiral L S R , tris[3-heptafluoropropyl-
hydroxymethylene)-( + )-camphorato europium] [Eu(hfc) 3], is described.
Carvone is the major constituent in the essential oils of the ripe fruits
III. Terpenoids 189
from caraway (51.2%) and of the fresh leaves from Menta spicata ( 6 9 . 9 % ) . It
exists in two enantiomeric forms and has different physical and physiological
properties. S( + ) carvone has a caraway odour, and is detectable at rather
high threshold. It is used as a starting material for the synthesis of a pher-
omone component of the female California red scale (6). R ( - ) carvone has a
spearmint odor, is detectable at a lower threshold than S( + ) and is used as a
starting material in the preparation of picrotoxinin (7).
The enantiomeric purity of S( + ) and R ( - ) carvones, isolated from
natural oils, is easily determined by NMR-polarimetry using L S R .
2. Apparatus
Flash chromatography assembly
Gas Chromatograph
NMR instrument
3. Materials
Caraway seeds Eu(hfc) 3 Silica gel 60Â
Chromosorb W Hexane Spearmint seeds
Ethyl acetate
4. Procedure
Each of the commercial variety of Mentha spicata (received from a nursery)
and ripe fruit of caraway are steam-distilled for 1 hr. The essential oils are
dried over anhydrous sodium sulfate. Carvone is isolated from the oil by flash
chromatography (as described in the experiment Flash Chromatography of
Essential Oil Constituents, p. 200) on silica gel Davisil 60Â, 200-425 mesh, and
eluted by 1 to 5 % solution of ethyl acetate in hexane. The chemical purities of
natural and commercial samples of carvone are detected by gas chromatogra-
phy on a packed glass column (3m x 4mm inside diameter [i.d.]) with 5 %
Carbowax 20M on acid-washed silanized Chromosorb W (80-100 mesh).
Operating conditions: temperature programming 70-200°C (5°C/min), car-
rier gas nitrogen, flow 30 ml/min. Optical rotations are measured (in ethanol)
using a Polarimeter.
Before the determination of the enantiomeric composition of natural
carvone, it is essential to carry out the N M R measurements of a mixture of
the two synthetic enantiomers of carvone in the presence of the chiral shift
reagent Eu(hfc) 3. (The pure synthetic enantiomers can be obtained from
certain chemical companies). These measurements provide an important
information regarding the L : S (lanthanide to substrate) ratio, which leads to
a good separation of the two synthetic enantiomers and hence for the natural
enantiomeric mixture (such as (S)-( + ) and (R)-(-)-carvones).
Equal volumes (5 μΐ) of each of the S and 7?-carvones (1:1 ratio), are
placed in a NMR tube, 300 μ\ of deuterochloroform (CDC1 3) and 50 μΐ of 1%
Tetramethyl silane (TMS) in deuterochloroform are added. The NMR spec-
trum shows no difference of the two enantiomers (there is no separation in
NMR signals of the nuclei near asymmetric carbon). The Eu(hfc) 3 shift
reagent is then added portionwise to the NMR tube (the first portion is 5 mg,
—3.7 /zmole) and the N M R spectra are recorded until the splitting of the
olefinic C 7 methyl protons singlet is observed. In order to determine which
JAi mJDu
ppm 8 7 6 5 4 3 2 ppm 8 7 6 5 4 3 2
ppm 8 7 6
IP
5 4 3 2
1
Figure 3.1 A: H - N M1 R spectra of (S)-(^)-carvone with Eu(hfc) 3 at
[L]/[S] = 0 . 7 - 0 . 8 ; B: H - N M R spectra of (R)-(-)-carvone with Eu(hfc) 3 at
[L]/[S] = 0 . 7 - 0 . 8 ; C: ' H - N M R spectra of (RS)-carvone with Eu(hfc) 3 at
[L]/[S] = 0 . 7 - 0 . 8 .
III. Terpenoids 191
peak corresponds to the S and the R enantiomer, the ratio of the two
enantiomers is increased to 1:2.
Having found the right conditions and the L : S ratio for the satisfactory
separation of the synthetic enantiomers, the natural product is measured
using the same L : S ratio. The fact that there is no splitting of the singlet of
the allylic C-7 methyl protons in the NMR spectrum confirms the enantio-
meric purity of the natural product.
In Figs. 3-1 ( a - c ) , the *H-NMR spectra of R, S, and ivS-carvones with
Eu(hfc) 3 reagent at [L]/[S] = 0.7-0.8 is presented.
References
1. Sullivan, G. R . (1978). Topics in Stereochemistry 10, 287.
2. Martin, M. L . , Delpuech, J . J . , and Martin, G. J . (1980). "Practical N M R Spectroscopy/'
Heyden and Sons, London.
3. McCreary, M. D . , Lewis, D . W., Warnick, D . L . , and Whitesides, G. M. (1974). / . Amer.
Chem. Soc. 96, 1038.
4. Plummer, Ε . L . , Stewart, T. Ε . , Pyrne, Κ . , Pierce, C. T . , and Silverstein, R . M. (1976). J.
Chem. Ecol. 2, 307.
5. Borden, J . H., Handley, J . R . , McLean, J . Α . , Silverstein, R . M., Chang, L . , Slesser,
Κ. N., Johnson, B . D . , and Shuler, H. R . (1980). J. Chem. Eco. 6, 445.
6. Roelfs, W., Gieselmann, M., Carde, Α . , Tashiro, H., Moreno, D. S., Henrick, C. Α . , and
Anderson, R . J . (1978). J. Chem. Ecol. 4, 211.
7. Corey, E . J . , and Pearce, H. L . (1979). J. Amer. Chem. Soc. 101, 5841.
8. Ravid, U . , Bassat, M., Putievsky, E . , Weinstein, V . , and Ikan, R . (1987). Flavour and
Fragrance Journal 2, 95.
Recommended Reviews
1. Pruthi, J . S. (1980). Academic Press, "Spices and Condiments: Chemistry, Microbiology,
Technology."
2. Ravid, U . , Putievsky, E . , Bassat, M., Ikan, R . , and Weinstein, V . (1988). Determination of
the enantiomeric composition of natural and nature-identical semiochemicals by 'H-NMR
"polarimetry." In "Bioflavour ' 8 7 " (P. Schreier, (ed.), p. 97. Walter de Gruyter and Co.
3. Ravid, U . , Putievsky, E . , Bassat, M., Ikan, R . , and Weinstein, V . (1988). The use of chiral
lanthanide shift reagent to determine the enantiomeric purity of some essential oil consti-
tuents. Flavour and Fragrance Journal 3, 117.
D. Transformation of α-Pinene to Camphor

1. Introduction
α-Pinene is widely distributed in nature. It is present in the majority of the
essential oils of conifers and is the principal constituent of turpentine oil. The
name pinene was selected to indicate its association with the various species
of Pinus. B y a series of transformations, it is possible to convert α-pinene to
camphor. Pinene hydrochloride is stable only at low temperatures and readily
undergoes rearrangement to form bornyl chloride. Furthermore, the dehyd-

rochlorination of bornyl chloride with a base does not yield the expected
bornylene, but camphene. On treatment with acetic anhydride, camphene
forms isobornyl acetate, which is treated with a base to form isoborneol.
Upon oxidation with chromic acid, isoborneol yields camphor.
Camphor is used as a counterirritant, anesthetic, and mild antiseptic.
CH3 CH3 CH2
α-Pinene Bornyl chloride Camphene
2. Principle
Many rearrangements of terpenes are of the Wagner-Meerwein type, which
take place via the formation of a carbonium ion. They may be divided into
two groups—eliminative and noneliminative changes.
The first stage of the transformation of α-pinene to camphor, the trans-
formation of pinene hydrochloride into bornyl chloride, probably proceeds by
the following mechanism:
Pinene hydrochloride Hybrid carbonium ion Bornyl chloride
The formation of camphene from bornyl chloride, a typical elimination

reaction proceeds via a similar mechanism:
Bornyl chloride Hybrid carbonium ion Camphene

III. Terpenoids 193
The stereospecificity of the rearrangement of camphene hydrochloride

to isobornyl chloride requires a special explanation. Representing camphene
hydrochloride by the stereochemical formula 1, we see that the positively
charged organic moiety resulting from chloride anion extraction can be repre-
sented by resonance hybrid forms 2a, 2b, and 2c, or by cation 2. Such a
species, in which the positive charge is delocalized by means of a multicenter
molecular orbital formed by sigma overlap of atomic orbitals, is called a
non-classical carbonium ion.
HCl -cr
Camphene Camphene hydrochloride
Alkaline hydrolysis of isobornyl acetate forms isoborneol, which is oxi-

dized to camphor by means of chromic acid.
KOH
OOCCH3
Isobornyl acetate
Camphor
3. Apparatus
Steam generator
Materials
Acetic acid Potassium hydroxide
Acetone Sodium acetate
Chloroform Sodium bicarbonate
Chromium trioxide Sodium carbonate
Ethanol Sulfuric acid
Hydrochloric acid, dry Turpentine
5. Time
10 hours
6. Procedure
a. Isolation of α-pinene from turpentine oil

A reasonable amount of commercial turpentine oil is dried with sodium
sulfate and fractionally distilled. α-Pinene distills at 154 to 155°C and ß-
pinene, at 163 to 164°C.
b. Pinene hydrochloride
Pure pinene is mixed in a flask with an equal volume of chloroform, the flask
is cooled below 0°C, and dry hydrochloric acid (gas) is bubbled through the
solution until it becomes saturated. An equal volume of water is added, and
excess acid is neutralized with sodium bicarbonate. The mixture is immedi-
ately subjected to steam distillation; the product solidifies and is recrystal-
lized from ethanol; mp 130-131°C.
c. Camphene
One part pinene hydrochloride is mixed with one part sodium acetate (freshly
fused) and two parts glacial acetic acid, and heated at 200°C for 3 to 4 hr.
Steam distillation gives pure DL-camphene; mp 50°C, bp 159-160°C.
d. NMR spectrum of camphene
Position δ (ppm)
a 1.01
1.52
c 1.52
e. Isobornyl acetate
Camphene (10 g) in 30 ml acetic acid and 2 ml 5 0 % sulfuric acid are heated
on a water bath for 20 min. Twenty ml water is added, and the mixture is
allowed to cool. The ester is separated and washed with dilute sodium
carbonate and water, and dried. It is then distilled under reduced pressure;
bp 105°C/15 mm; yield, 10 g.
f. Isoborneol
Ten g isobornyl acetate and 5 g potassium hydroxide in 30 ml ethanol and
10 ml water are refluxed for 1 hr on a water bath. Cold water is added, and
III. Terpenoids 195
the solidified isoborneol is filtered off on a Büchner funnel and washed with
water; yield, 8 g.
g. Camphor
To 5 g isoborneol in 10 ml acetone is added 7 ml of a solution prepared by
dissolving 18 g chromium trioxide in 16 ml sulfuric acid. 30 ml water is then
added, and the mixture is left for 1 hr at room temperature. It is then
subjected to steam distillation, and the solid camphor is filtered and washed
with water; yield, 2 g. Sublimation yields pure camphor, mp 176°C.
h. UV Spectrum of camphor
Η
Λ*£ 289m^ (loge 1.51)
The peak is due to carbonyl absorption.
i. NMR Spectrum of camphor
Hie)
Position δ (ppm)
a 0.86
b 0.97
c 1.49
d 1.71
e 2.04
Recommended Reviews
1. Berson, J . A . (1964). Carbonium ion rearrangements in bridged bicyclic systems. In "Molecu-
lar Rearrangements" (P. de Mayo, ed.), Vol. 1, p. 111. Interscience, New York.
2. Sargent, G . D . (1966). Bridged, non-classical carbonium ions. Quart. Revs. 20, 301.
E. Photoprotonation of Limonene to p-Menth-8-en-1-yl Methyl Ether
Limonene /?-Menth-8-en-l-yl
Methyl Ether
1. Introduction
Acid-catalyzed ground state additions to limonene generally afford a mixture
of products resulting from competing protonation of both double bonds. The
photoprotonation of cycloalkenes, described in this procedure, is believed to
proceed via initial light-induced eis —» trans isomerization of the alkene. The
resulting highly strained trans isomer undergoes facile protonation.
2. Principle
The following (1) procedure permits the protonation of cyclohexenes and
cycloheptenes under neutral and mildly acidic conditions. In addition to
facilitating protonation of cycloalkenes, the procedure affords a means of
selectively protonating a double bond located in a six- or seven-membered
ring, in the presence of another double bond contained in a acyclic, exo-
cyclic, or larger-ring cyclic environment.
3. Apparatus
Photochemical reactor
Gas Chromatograph equipped with a stainless steel column (3m x 3.2m)
packed with 2 0 % SF-96 on Chromosorb W.
4. Materials
(+)-Limonene Phenol
Methanol Sodium hydroxide
5. Time
48 hours for complete conversion
6. Procedure
A 250-ml photochemical reactor (Fig. 3.2) (equipped with a 450 watt Hanovia
mercury lamp, a water-cooled condenser, and a trap filled with methanol) is
flushed with nitrogen and charged with a solution of 20 g (+)-limonene, 5 g
phenol, and 5 drops concentrated sulfuric acid in 210 ml anhydrous meth-
anol. Water flow through the condenser is started, and the nitrogen flow
is adjusted to provide agitation of the contents of the vessel. After 15 min,
irradiation is started and the reaction followed by GLC. A 3 m x 3.2 mm i.d.
stainless steel column packed with 2 0 % SF-96 on Chromosorb W (60-80
mesh) is used. The flow rate of helium is 60 ml/min. Temperature programming
10°C/min (from 50 to 200°C), the retention time of the eis and the trans isomers
are 17.9 and 18.7 min, respectively. About 48 hr is the approximate time needed
for essentially complete conversion. The solution is then poured into 900 ml 5 %
aqueous sodium hydroxide solution containing 125 g sodium chloride, and the
II. Terpenoids 197
To Ν
bubbler
H 2O i n —
N 20 source
Hanovia,
med. pressure
I
450-W HG lamp _ Trap 1
(empty)
Vycor
filter
Quartz
well
Photolyte
Glass frit Trap 2

(MeOH filled)
Figure 3.2 A 250-ml photochemical reactor with a 450-watt Hanovia mercury

lamp, a water-cooled condenser, and a trap filled with methanol.
mixture is extracted with two 100-ml portions of ether. The ether layers are
combined, washed with 50 ml saturated sodium chloride solution, and dried
over anhydrous sodium sulfate. The drying agent is removed by filtration, and
the filtrate is concentrated under reduced pressure. The liquid is distilled at
reduced pressure through a short column. The material that distills at 90 to 95°C
(10 mm) consists of a mixture of eis- and frYms-/?-menth-8-en-l-yl methyl ether;
yield, 13 g.
The products can be checked by G L C using 2.4 m x 3.2 mm i.d. stainless
steel column packed with 7% SE-30 on Chromosorb W (60-80 mesh) at 160°C.
The retention time of the trans isomer is 1.6 min, and that of eis is 1.8 min ; flow
rate of helium is 55 ml/min.
1
a. IR (neat) cm
3080 ( = C — H ) ; 2964, 2939, 2860, 2825 ( C — H ) , 1645 ( C = C ) ; 1464,1453 and
1442 (overlapping peaks): 1370, 1124 and 1082 ( C — O C ) ; 885 ( = C H ) .
1
b. H NMR (CDCI2)
S 1 . 1 0 [ s , 3 H , C H 3 (trans)], 1.19 [ s , 3 H , C H 3 (eis)], 1.30-2.00 (8H,CH 2 —)» 1.71
[s, 3H, C H 3 (cis/trans)], 3.14 [s, 3H, O C H 3 (trans)] ,3.21 [s, 3H, O C H 3 , (eis)],
4.69 [s, 2H, = C H 2 (cis/trans)].
Reference
1. Tise, F . P., and Kropp, P. J . , (1983). Org. Synth., 6 1 , 112.
Recommended Reviews
1. Kropp, P. J . (1978). Photochemistry of alkenes in solution. Molecular Photochemistry 9, 39.
2. Schuster, D . I. (1987). Organic photochemistry. In "Encyclopedia of Physical Science and
Technology," Vol. 10, p. 375. Academic Press, New York.
F. Flash Chromatography of Essential-Oil Constituents

1. Introduction
Essential oils are complex and volatile mixtures of terpenoids and phenylpro-
pane derivatives. The number of components in any single oil may vary from
a few to over 100. These multicomponent mixtures make the analysis of the
oils by GC rather difficult because of the overlap of peaks and similarity of
retention times. Thus, column chromatographic prefractionation of the oils
before the GC analysis is of prime importance. The conventional long column
chromatography for separating complex mixtures of organic compounds is
time consuming and frequently gives poor recovery owing to band tailing.
A substantially faster technique for the separation of complex mixtures is
flash chromatography. It is basically an air pressure-driven hybrid of me-
dium pressure and short column chromatography, which has been optimized
for rapid separations. The apparatus required for this technique consists
of a chromatography column, nitrogen cylinder, and a flow-controller valve.
The flash chromatographic technique can be summarized as follows:
1. A solvent is chosen that gives a good separation and moves the
desired component to 7?f ~ 0.3 on analytical T L C ;
2. The column of appropriate diameter is selected. The ratio of the
essential oil and the adsorbent (such as silica gel (40-60 μτη) is about
1:30;
3. The column is filled with nonpolar solvent, and pressure is used on the
top to rapidly push all the air from the silica gel; and
4. The sample is applied, and the column is refilled with the solvent and
eluted at a flow rate of 2in/min.
Fractions are monitored by T L C (using UV-detection lamp or sprayed
with an appropriate chromogenic reagent such as 2,4-DNP). Increasing
III. Terpenoids 199
amounts of ethyl acetate in hexane or petroleum ether appeared to be the

most generally satisfactory eluant. The order of elution of essential o i l -
oxygenated constituents with an increasing gradient of ethyl acetate in hexane
is as follows: oxides, esters, ketones, and alcohols.
2. Principle
Carvone is a natural terpenoid ketone found in the essential oils of caraway
seeds and the spearmint plant. The fact that caraway and spearmint exhibit
distinctly different odors suggests that the carvones occurring in these oils are
stereoisomers. The relatively polar carvone is adsorbed more strongly by
silica gel than are the terpenoid hydrocarbons (and other components), which
can be eluted from the column by a nonpolar solvent such as hexane. The
polarity can then be increased by adding increasing amounts of ethyl acetate
to elute the carvone. The optical rotations and the infrared spectra of the en-
antiomeric carvones are then measured by a Polarimeter.
3. Apparatus
Glass column for flash chromatography
4. Materials
Clean sand
Hexane
Ethyl acetate
Essential oils of caraway, spearmint, thyme, nutmeg, clary sage,
lavender, citrus
Silica gel ( 4 0 - 6 0 mesh)
Microscope T L C plates.
5. Procedure
Having chosen a column of the appropriate diameter, a small plug of glass
wool (A) is placed in the tube connecting the teflon stopcock and the column
body, or preferably a sintered glass disc is fused here. Dried 4 0 - 6 0 mesh silica
gel is poured into the column in a single portion to give a depth of 5.5 to 6 in.
The column is then gently tapped vertically on the bench top to pack the gel.
Next, a 1/8-inch layer of sand is carefully placed on the flat top of the dry gel
bed, and the column is clamped for pressure packing and elution. The solvent
chosen is then poured carefully over the sand to fill the column completely.
The stopcock of the flow controller (Fig. 3.3) is opened all the way; this will
cause the pressure of nitrogen (or air) above the adsorbent layer to climb
rapidly and compress the silica gel, as solvent is rapidly forced through the
column. It is important to maintain the pressure until the air is expelled. The
A Ο ))))))}
7\
r
18" Air
Flow controller
Figure 3.3 Flash chromatography column with (A) small plug of glass wool,
and (B) stopcock of flow controller.
pressure is then released and excess eluant is forced out of the column. The
essential oil (of caraway or spearmint) is applied by a pipette as a 2 0 %
solution in the eluant to the top of the adsorbed bed, and the pressure is
applied to push all the sample into the silica gel (for each gram of oil, 30 g of
silica gel is used). The flow of nitrogen is then adjusted to cause the surface of
the solvent in the column to fall 2.0in/min. The fractions eluted are checked
on T L C plates as described in the introduction. The fractions containing
various series of compounds (hydrocarbons, acetates, ethers, ketones, alco-
hols) are then run on GC columns and finally identified by G C / M S , I R , NMR
and other techniques. Note: Never let the upper part of the adsorbent in the
column get dry!
Recommended Reviews
1. Clark-Still, W . , Kahn, M . , and Mitra, Α . (1978). Rapid chromatographic technique for
preparative separations with moderate resolution. J. Org. Chem. 43, 4923.
III. Terpenoids 201
2. Crane, L. J . , Zief, M., and Howarth, J . (1981). Low-pressure preparative liquid chroma-
tography. American Laboratory.
3. Rogers, J . A. (1981). Essential oils. In "Kirk-Othmer Encyclopedia of Chemical Technolo-
gy," Vol. 16, p. 307. John Whiley.
G. Isolation and Determination of Grape and Wine Aroma

Constituents
1. Introduction
The aromatic compounds of some grape varieties are present in the berry
either in a free state or bound to sugars in the form of glycosides. ( 1 - 3 ) The
free forms are present in different quantities in different varieties; in muscats
in particular, they form the major part of the aroma and consist essentially of
terpenols in various states of oxidation and of terpenoid polyols (Fig. 3.4).
HO
G H ι J
^ ^ ) H
OH OH
Κ
L
Figure 3.4 Aromatic compounds of grape varieties, including (A) linalool;

(B) geraniol; (C) nerol; (D) citronellol; (E) hotrienol; (F) p-menth-1-ene-9-ol;
(G) ds-furan-linalool oxide; (H) iriws-furan-linalool oxide; (I) ds-pyran-linalool
oxide; (J) trans-pyran-linalool oxide; (K) 3,7-dimethylocta-1-ene-3,7-diol; and
(L) 3,7-dimethylocta-1,5-diene-3,7-diol (and also benzyl- and 2-phenylethyl
alcohols).
The nonvolatile, nonaromatic bound fraction consists of disaccharide

glycosides, namely a, L-arabinofuranosyl-/3-D-glucopyranosides or a, L-rham-
nofuranosyl-/3, D-glucopyranosides, the aglycone of which is a terpenol, such
as geraniol, linalool and nerol, a terpene diol, 2-phenylethanol, and benzyl
alcohol.
2. Principle
In the following procedure ( 4 ) , the free and the bound aromas of grape juice
or wine are separated on X A D - 2 column. The bound fraction (terpene
glycosides) is cleaved by an enzyme (Pectinol) into free terpenes and sugars.
The free terpenes of both fractions are determined by GC on capillary
column.
3. Apparatus
Centrifuge Glass capillary column
Gas Chromatograph Mixer
4. Materials
Amberlite X A D - 2 resin Geraniol 2-Octanol
Benzyl alcohol Grapes Pectinol
Citrate-phosphate buffer Hydrogen (cylinder) Pentane
Diethyl ether Linalool Phenylethyl
Ethanol Methanol alcohol
Ethyl acetate Nerol Sorbic acid
Wine
5. Time
15 hours
6. Procedure
a. Plant material
Fresh grapes or wines can be used.
b. Juices and wines

Fresh grapes are cooled to 1°C immediately after picking, then crushed and
pressed, and the juice is centrifuged (9000 rpm, 15 min). All these opera-
tions should be carried out at 1°C. Sorbic acid (200 ppm) is then added to
the clarified juice. When the analysis is to be carried out some time after the
picking, immediately after harvesting, the grapes are deep-frozen at —20°C
and stored at this temperature. They are thawed to 1°C just before analysis
and then crushed in a whirlmixer; the pulp is filtered through gauze and
III. Terpenoids 203
centrifugea at the same temperature. The clear juice is stabilized with sorbic
acid. Wines are diluted in an equal volume of water before analysis.
c. Column preparation
Amberlite X A D - 2 resin suspended in methanol is poured into a glass column
( 3 5 x l c m i . d . ) whose lower part is fitted with a Teflon stopcock and a
glass-wool layer. The packed column should contain about 10 cm resin. Sev-
eral 25 ml volumes of methanol and then of diethyl ether are passed through
it, followed finally by 50ml distilled water. The column is now ready for use.
d. Fractionation and determination of free and bound fractions of the aroma

A sample of 50 to 100 ml of juice or wine is passed through the column with 10 μΐ
of 0 . 1 % solution of 2-octanol in ethanol (added as internal standard). The flow
rate is about 2 to 2.5 ml/min. The column is then rinsed with 50 ml of water to
eliminate sugars, acids, and other water-soluble constituents.
e. Fractionation of the free fraction

The free fraction of the aroma fixed on the column is eluted using 50 ml of
pentane at a flow rate of 2 to 2.5 ml. The pentane extract is dried over
anhydrous sodium sulfate, filtered, and concentrated to a final volume of
50 μΐ by distillation at 40°C. The concentrate is used for GC analysis.
f. Fractionation of the bound fraction

After the elution of the free fraction, the bound fraction is eluted with 50ml
of ethyl acetate. It is then dried over anhydrous sodium sulfate, filtered and
concentrated, first to 1 ml under vacuum at 40°C, and then to dryness at 45°C,
using a stream of nitrogen.
g. Hydrolysis of the bound fraction

_ 1
To the above dry glycoside extract is added 0.1ml of 2 x 1 0 M , citrate-
phosphate buffer, pH 5.0. The solution is washed four times with 0.1ml
pentane to eliminate possible traces of the free fraction, using strong agitation
1
in a whirlmixer. Pectinol solution (0.4 mg of Pectinol in 0.1 ml of 2 x 1 0 " M ,
citrate-phosphate buffer, pH 5) is then added to the glycoside solution. After
agitation, the mixture is poured into an ampule, hermetically sealed, and
placed in a water bath for 12 hr at 40°C. The medium is then extracted five
times with 0.1 ml pentane. After addition of 10 /xl 0 . 1 % solution of 2-octanol
in ethanol, the solvent is eliminated by distillation at 40°C to give a final
volume of 40 μΐ. The extract is then used for GC analysis.
h. Gas-chromatographic analysis of aroma constituents

The terpenoid alcohols (geraniol, nerol linalool) and benzyl- and 2-
phenylethyl alcohols are determined on GC equipped with a glass capillary
column (70 m x 0.5 mm i.d.) coated with 0.3 μπι of free fatty acid phase and
connected to an integrator. The fractionation is carried out first at a constant
temperature of 70°C for 5 min, then with a temperature gradient from 70° to
180°C at a rate of 2°C/min, and finally at a constant temperature of 180°C for
30 min. The carrier gas (hydrogen) flow rate is 25 ml/min. The volumes of
pentane extracts injected are between 2 and 3 μ\.
i. Notes
1. The choice of pentane for free terpenol elution is the result of a
compromise: a more polar solvent like dichloromethane gives a better
elution of these compounds, but also removes part of the glycosides.
Pentane does not elute glycosides but does not enable full recovery of
free terpenols. Ethyl acetate elutes glycosides as well as methanol, but
the former is more selective.
2. The glycosidic part of the bound fraction usually consists of glucose,
rhamnose, and arabinose. The identity of the aglycones as determined
by GC-MS are the following terpenols: linalool, a-terpineol,
citronellol, nerol, and geraniol, together with linalool pyranic oxide, 3,
7-dimethyl-l, 5-octadiene-3, 7-diol, and two aromatic alcohols, benzyl-
and 2-phenylethyl alcohols.
3. Enzymatic hydrolysis of the glycosides is chosen as the best method;
an acid hydrolysis may induce considerable modification of the
terpenol composition (rearrangements of the nonterpenoid alcohols).
4. The bound terpenols (terpene glycosides) are the hidden aromatic
potential in grapes. Certain technological applications, such as
enzymatic cleavage of the bound forms and release of free terpenol
into medium, will increase the aromatic potential of wines.
References
1. Williams, P. J . , Strauss, C. R . , Wilson, B . , and Massy-Westropp, R . Α . , (1982). J. Agric.
Food Chem 30, 1219.
2. Williams, P. J . , Strauss, C. R . , Wilson, B . , and Massy-Westropp, R . A . (1982). / . Chroma-
togr. 235, 471.
3. Shoseyov, O., Bravdo, Β . Α . , Ikan, R . , and Chet, I. (1988). Phytochem. 27, 1973.
4. Gunata, Y . Z . , Bayonove, C. L . , Baumes, R . L . , and Cordonnier, R . E . (1985). J.
Chromatogr. 3 3 1 , 83.
Recommended Reviews
1. Rapp, Α . , Mandery, H., and Guntert, M . , (1984). Terpene compounds in wine. In "Proc.
Alko Symp. on Flavor Research of Alcoholic Beverages." ( L . Nykanen, and P. Lehtonen,
eds.), Vol. 3, p. 255.
2. Strauss, C. R . , Wilson, B . , Gooley, P. R . , and Williams, P. J . (1986). Role of monoterpenes
in grape and wine flavor. In "Biogeneration of Aromas." Amer. Chem. S o c , Symp. Series,
Vol. 317, p. 222.
III. Terpenoids 205
3. Montedoro, G . , and Bertuccioli, M., (1986). The flavour of wines, vermouth, and fortified
wines. In "Food Flavours, Part Β . " (I. D . Morton and A . J . Macleod, eds.), p. 171. Elsevier,
Amsterdam, the Netherlands.
4. Merritt, C., and Robertson, D . H. (1982). Techniques of analysis of flavours: Gas-
chromatography and mass spectrometry. In "Food Flavours, Part A . " (I. D . Morten and A.
J . MacLeod, eds.), p. 49. Elsevier, Amsterdam, the Netherlands.
H. Qualitative and Sensory Evaluation of Aromatic Herb

Constituents by Direct Headspace—Gas Chromatography
I. Introduction
Gas chromatographic methods in which the volatile components in the gas
space around liquid or solid samples are determined indirectly are known
under the general name of headspace-GC methods.
A sample from the equilibrated gas phase above the solid or liquid
phase is transferred either manually or automatically to the gas Chromato-
graph for analysis. The gas sample is either introduced directly into the GC
column, or concentrated using liquid or solid traps, and then transferred into
the column by means of thermal desorption or liquid extraction. HSGC
methods have been widely applied in the fields of environmental analysis,
clinical research, industrial processing, and quality control, as well as in
microbiological and food chemistry studies. HSGC is a rapid, simple, precise,
sensitive, and nondestructive technique. It has been used for the quality
control of aromatic herbs ( 1 - 3 ) and of wine (4).
Sensory analysis of GC effluent (GC-sniff) has been used by several
investigators to evaluate the aroma significance of separated components in
coffee (5), bilberries (6), peaches (7), and wine (8). In this way it is possible to
examine the substances responsible for the specific olfactory sensations ex-
cited by a particular product by evaluating the constituents of the odor.
2. Principle
Herb sample is ground in a glass grinder. After conditioning in a gas-tight
glass vial, the gaseous phase is transferred to a syringe and injected into a GC
coupled with a mass spectrometer. A series of volatile markers may be
injected into GC for comparative purposes.
A gas syringe is the most popular device for transferring a gaseous
sample of volatiles from the headspace vial into a gas Chromatograph
(Method 1). Apart from the contamination and adsorption problems with
such a device, there is a more serious drawback: a syringe is an open system
during the sample transfer. Any pressure that has been generated by the
increase of the partial vapor pressures of all the volatiles in the sample by
heating the vial, also extends into the syringe.
206 CHAPTER 3 isoprenoids
During sample transfer, however, the syringe needle is open to the

atmosphere, and an undefined amount of gas sample will be lost by expansion
of the headspace gas through the needle.
In order to get reproducible results, the volume and the pressure in the
sample must be held constant. This is achievable by using a sampling device as
described in method 2 (Fig. 3.5) in the procedure (9).
Both methods, the syringe and the sampling device, may be coupled
with a splitter for mass spectroscopic analysis.
3. Apparatus
Gas Chromatograph Headspace apparatus
GC column 50 m coated with QV-1 Thermostat bath
4. Materials
Herbs such as bitter orange, clary sage, caraway, coriander, lemon grass,
Mentha, peppermint, Salvia dominica, spearmint, sweet basil.
Monoterpenes (hydrocarbons, ketones, alcohols, etc.)
Syringe
Vials
5. Time
8 hours
6. Experimental
a. Method 1
A suitable sample of an herb such as Clary sage {Salvia sclarea L.) and Salvia
dominica L . ; lavender {Lavandula angustifolia Mill.), sweet basil {Ocimum
basilicum), coriander {Coriandrum sativum), sweet marjoram {Origanum
majorana L . ) , caraway {Carum carvi L . ) , spearmint {Mentha spicata L.) and
Mentha Iongifolia ( 2 ) , yarrow {Achillea millefolium), bitter orange {Citrus
aurantium), lemon tree {Citrus limonium), and peppermint {Mentha piper-
ita), is finely milled in a glass grinder, avoiding overheating. A weighed
amount of the ground herb ( l g ) is then put in a glass vial, sealed with a
rubber septum. After conditioning in a thermostat bath for 7 hr at 60°C, a
sample of the gaseous headspace is injected into a gas Chromatograph by
means of a syringe. The following operating conditions may be used: column,
50 m, OV-1 0.15 μτη stationary phase thickness; carrier gas, hydrogen, flow
rate 2 ml/min; splitting ratio, 1:4. Injector and flame ionization detector
temperatures, 200°C; oven temperature, from 20°C to 150°C at a rate of
3.5°C/min.
III. Terpenoids 207
In order to identify the volatile constituents, it is desirable to couple the

GC with a mass spectrometer. A separate injection should be used for the
sniffing of the GC effluent.
b. Method 2
The sampling device (Perkin-Elmer HS-100 Automatic Headspace Sampler)
comprises a heated movable sampling needle with two vents and a solenoid
valve, V j , in the carrier gas supply line. This needle moves up and down in a
heated cylinder and is sealed by three O-rings. In the standby position, the
lower needle vent is placed between the two lower O-rings and thus sealed
against atmosphere, while the carrier gas flows through valve V] to the
column. A small cross-flow purges the cylinder and is vented via valve V 2 .
At the end of the selected thermostating period, the sampling needle
descends, pierces the septum cap into the vial, and pressurizes it either up to
the head pressure of the column (as shown in Fig. 3.5) or to any other higher
pressure value, which is provided by an additional pressure regulator and a
solenoid valve. The latter arrangement is recommended for columns with a
small pressure drop, such as a wide-base capillary column. At elapse of the
preselected injection time (a few seconds), both valves open again. Carrier
gas streams to the column and branches in order to pressurize the sample
vial again. This immediately stops the injection, and the residual sample
ir„
Pressurization Sampling
Column
Carrier
gas K]
ι
Figure 3.5 Balanced pressure sampling with the Perkin-Elmer H S - 1 0 0

automatic headspace sampler.
vapors in the needle are flushed back into the vial, while the sample moves
through the GC column.
c. Quantitative analysis of the aroma composition

When a state of equilibrium is achieved, the phase distribution of a volatile
solute is determined by its partition coefficient Κ according to Equation 1,
and the peak size A in the resulting headspace chromatogram is thus pro-
portional to the gas phase concentration Cg (Equation 2 ) , while CI is the
concentration of the liquid sample.
[i] Κ Cl/Cg
[2] A Cg = C l / K
The application of external standards for comparative purposes is recom-

mended.
References
1. Gabri, S., and Chialva, F . J . (1981). High Resol. Chromatogr. and Chromatogr. Commun.
4, 215.
2. Chialva F . , Doglia, G . , Gabri, G . , and Ulian, F. (1983). J. Chromatogr. 279, 333.
3. Hiltunene, R . , Vuorela, H., and Laakso, L. (1985). In "Essential Oils and Aromatic
Plants." ( B . Svendsen and J . J . C. Sheffer (eds.), p. 23. Martinus Nijhoff and W. Junk,
Dordrecth, (1980). The Netherlands.
4. Noble, A . C , Flalth, R . Α . , and Forrey, R . R. (1980). Agric. Food Chem. 28, 346.
5. Tassan, C , and Russell, G. F. (1974). J. Food Sei. 39, 64.
6. Von Sydow, E . , Anderson, J . , Anjon, K., and Karlsson, G. (1970). Lebensm.-Wiss. Tech-
nol. 3, 11.
7. Spencer, M., Panghorn, R . M., and Jennings, W. G. (1978). / . Agric. Food Chem. 26, 725.
8. Rapp, Α . , Hastrich, H., Enel, L . , and Knipser, W. (1978). "Flavor in Foods and Bever-
ages." Academic Press, New York.
9. Kolb, B . (1985). In Essential Oils and Aromatic Plants. (A. B . Svendsen and J . J . C. Scheffer
eds.), p. 3. Martinus Nijhoff/Dr. W. Junk. Boston, Massachusetts.
Recommended Reviews
1. Bauer, K . , and Garbe, D . (1985). "Common Fragrance and Flavor Materials." V C H
Publishers, Weinheim, F R G .
2. Cagen, R . H., and Kare, M. R . (1981). "Biochemistry of Taste and Olfaction." Academic
Press, New York.
3. Charalambous, G . , (ed.) (1978). "Analysis of Foods and Beverages. Headspace Tech-
niques." Academic Press, New York.
4. Lawrence, B . M., Mookherjee, B . D . , and Willis, B . J . , (eds.). (1988). "Flavors and
Fragrances: A World Perspective." Elsevier, Amsterdam, The Netherlands.
5. Nunez, A. J . , and Gonzalez, L. F . (1984). Preconcentration of headspace volatiles for trace
organic analysis by gas chromatography. / . Chromatogr, 127, 300.
III. Terpenoids 209
I. Preparation of Abietic Acid from Wood Rosin and Its

Dehydrogenation to Retene
CH3 CH3
Retene Abietic acid
1. Introduction
The oleoresinous exudate of conifers, mainly pines, can be separated into two
components—rosin and turpentine. Turpentine is generally removed from
oleoresin by steam distillation, and rosin remains in the still as a nonvolatile
residue. Rosin is known as naval stores, as it was used for caulking the hulls of
ships.
Rosin consists mainly of isomeric diterpenoid acids having an empirical
formula C 2 o H 3 0 0 2 . Abietic acid is the most abundant resin acid; it can also be
prepared by acid-catalyzed isomerization of other natural resin acids (1).
Abietic acid has been purified through its diamylamine, piperidine, and
brucine salts (2).
The nature of the ring system of abietic acid was established by dehy-
drogenation with sulfur to retene (3), and was identified as l-methyl-7-
isopropylphenanthrene by oxidative degradation and by synthesis.
2. Principle
Rosin is isomerized by refluxing in a solution of ethanol-hydrochloric acid for
2 hr (4).
Abietic acid is then isolated from the isomerized rosin by formation of

the diamylamine salt; its crystallization and acidification with acetic acid
affords pure abietic acid. On dehydrogenation with sulfur, abietic acid forms
retene, identified as a picrate.
3. Materials
Acetic acid Ethanol, 9 5 % Sodium hydroxide
Acetone Ether Sulfur
Carbon dioxide Hydrochloric acid Wood rosin
Diamylamine
4. Time
5 - 6 hours
5. Procedure
a. Preparation of abietic acid
Into a 2-liter round-bottomed flask fitted with a 35-cm reflux condenser are
introduced 250 g wood rosin, 740 ml 9 5 % ethanol, and 42 ml hydrochloric
acid. A stream of carbon dioxide is passed over the surface of the solution
through a glass tube during this reaction. The mixture is boiled under reflux
for 2 hr. At the end of this period, the ethanol and acid are removed by steam
distillation, and the water is decanted. The residue is cooled to room temper-
ature and dissolved in 1 liter ether. The ether solution is extracted with water
and dried over anhydrous sodium sulfate. Evaporation of ether in vacuo
yields 245 g isomerized rosin, which is placed in a 1-liter Erlenmeyer flask and
dissolved in 375 ml acetone by heating the mixture on a steam bath. To this
solution at incipient boiling are added slowly, with vigorous agitation, 127 g
diamylamine. Upon cooling to room temperature, crystals appear in the form
of rosettes. The mass in agitated, cooled well in an ice bath, and filtered
by suction. The crystalline salt is washed on a Büchner funnel with 150 ml
acetone and dried in a vacuum oven at 50°C for 1 hr. The solid is recrystal-
lized four times from acetone. Each time a sufficient quantity (20 ml per
gram) of acetone is used to ensure complete solution, and the solvent is evap-
2 4
orated until incipient precipitation of the salt; yield, 118 g; [ a ] D - 6 0 ° .
The amine salt is placed in a 4-liter Erlenmeyer flask and dissolved in
1 liter 9 5 % ethanol by heating the mixture on a steam bath. To the solution,
which has been cooled to room temperature, is added 36 ml glacial acetic
acid. The resulting solution is stirred, 900 ml water is added, at first cautiously
and with vigorous agitation, until crystals of abietic acid begin to appear; the
remainder of the water is then added more rapidly. The abietic acid is
collected on a Büchner funnel and washed with water until the acetic acid has
III. Terpenoids 211
been removed completely, as indicated by tests with indicator paper. Recrys-

tallization can be effected by dissolving the crude product in 700 ml 9 5 %
ethanol, adding 600 ml water as described above, and cooling the solution.
The yield of abietic acid is 98 g ( 4 0 % based on the weight of isomerized
4
rosin); [afe -106°.
1
b. H-NMR
(c) (/)
δ (ppm)
0.67
0.83 (doublet)
1.18
1.96
5.68
12.45
c. Abietic Acid
13
d. C NMR
C-l 38.3 C-8 135.5 C-15 34.8
C-2 18.1 C-9 51.0 C-16 20.9
C-3 37.2 C-10 34.5 C-17 21.4
C-4 46.3 C-11 22.5 C-18 185.4
C-5 44.9 C-12 27.5 C-19 16.7
C-6 25.6 C-13 145.1 C-20 14.0
C-7 120.5 C-14 122.5
e. Mass Spectrum
Abietic Acid C20H30O2, Mol. wt. 302.
m/z 302(62%) 105(78%) 91(100%) 77(56%)
121(49%) 93(49%) 79(55%) 67(45%)
f. UV Spectrum of abietic acid

Η
λ*° 237 ταμ (loge 4.2)
Abietic acid is a heteroannular conjugated diene in which the two double
bonds are conjugated, but located in two adjoining rings; the parent
homoannular diene has an absorption maximum at 253 m/x.
g. Dehydrogenation of abietic acid to retene

Abietic acid, 50 g, and 25 g sulfur are heated at 200°C (in a hood) until
hydrogen sulfide begins to evolve more slowly; heating at 250°C is then con-
tinued for a short period. The crude product is distilled under reduced pres-
sure; bp 260-270°C/20 mm; yield, 11-12 g.
The solid distillate is extracted with ether, and the ethereal solution is
washed with alkaline solution. Crystallization of the residue (after removal
of ether) from ethanol yields 3 g crystals of mp 98-99°C; the picrate melts
at 127°C.
References
1. Ruzicka, L . , and Meyer, J . (1922). Helv. Chim. Acta 5, 315.
2. Lombard, R . , and Frey, J . M. (1948). Bull. Soc. Chim. France 1194.
3. Vesterberg, A. (1903). Ber. 36, 4200.
4. Wheeler, T . S. (1963). Org. Synth. Coll. 4, 478.
Recommended Reviews
1. Barton, D . H. R . (1949). The chemistry of the diterpenoids. Quart. Revs. 3, 36.
2. McCrindte, R . , and Overtone, Κ. H. (1965). The chemistry of the cyclic diterpenoids. In
"Advances in Organic Chemistry" ( R . A. Raphael, E . C. Taylor, and H. Wynberg, eds.),
Vol. 5, p. 472. Interscience, New York.
3. Weaver, J . C. (1982). Natural resins. In "Kirk-Othmer Encyclopedia of Chemical Tech-
nology" Vol. 20, p. 197. Wiley, New York.
J. Conversion of Betulin to Alio- and Oxyallobetulin

1. Introduction
Betulin is one of the more plentiful triterpenes and was first isolated from the
bark of the birch tree in 1836 (1). It constitutes up to 2 5 % of the extractable
part of the outer bark of the white birch (Betula alba) (2), and as much as
3 5 % in the case of Manchurian white birch (Betula platyphylla) (3). Betulin
also occurs in the bark of Cory lus avellana (4) and Lophopetalum toxicum (5),
in rose hips (6), in brown coal (7), in lignite (8), and in the cactus Lemai-
reocereus griseus (9).
Betulin may be converted to the lactone, oxyallobetulin, by the ac-
III. Terpenoids 213
AUobetulin Oxyallobetulin acetate
tion of formic acid (10) or hydrobromic acid (11), followed by C r 0 3 oxida-

tion (12). This sequence of reactions connects the lupeol and /3-amyrin series
of the terpenoids.
2. Principle
Birch bark is extracted with a hot solution of sodium carbonate to remove
any acidic constituents. Betulin is then extracted with methanol. The betulin
may be isomerized to allobetulin by treatment with hydrobromic acid or
with formic acid followed by alkali. Acetylation of allobetulin, followed
by oxidation with chromium trioxide and hydrolysis, gives the lactone,
oxyallobetullin.
3. Apparatus
Chromatography column
4. Materials
Alumina Acetic anhydride Benzene
Acetic acid Bark of birch tree Chloroform
Chromium trioxide Formic acid Potassium hydroxide

Ethanol Hydrobromic acid Sodium carbonate
Ether Methanol
5. Time
7 hours
6. Procedure
a. Isolation of betulin
Birch bark (150 g) is cut into small pieces and boiled in an Erlenmeyer flask
with 2 % sodium carbonate solution. The contents are filtered, and the residue
is boiled twice with 500-ml portions of hot water, and filtered on a Büchner
funnel. The solid residue is dried in air, extracted with hot methanol for 3 hr,
and filtered. On concentration of the filtrate, crude betulin separates as white
crystals. The esters of betulin, remaining in the mother liquor, can be sapo-
nified by adding 25 volumes 1% ethanolic potassium hydroxide and leaving
overnight at room temperature. Crude betulin is filtered, dried, and crystal-
lized once from benzene and once from ethanol; needles, mp 251-252°C.
b. 3/3-Betulin [Lupendiol]
30 29
1 3
c. C NMR
C-l 38.7 C-8 41.0 C-15 27.1
C-2 27.4 C-9 50.5 C-16 29.2
C-3 79.1 C-10 37.3 C-17 47.9
C-4 38.8 C-11 20.9 C-18 47.9
C-5 55.3 C-12 25.2 C-19 48.8
C-6 18.3 C-13 37.2 C-20 150.5
C-7 34.3 C-14 42.8 C-21 29.8
III. Terpenoids 215
C-22 34.1 C-24 15.4 C-26 16.1 C-28 60.6 C-30 109.7
C-23 28.1 C-25 16.1 C-27 14.8 C-29 19.1
d. Mass Spectrum
3/3-Betulin [Lupendiol] C30H50O2, Mol. wt. 442.
m/z 442(38.46%) 203(71%) 135(69%) 95(78%)
411(64%) 189(100%) 121(51%) 81(53%)
207(75%)
e. IR Spectrum of betulin (in KBr)

- 1
3420 c m : Ο—H stretching
1645: C = C stretching of terminal methylene
1450, 1380: asym. and sym. C H 3
1075: C—Ο stretching of secondary OH
1030: C—Ο stretching of primary OH
880: out-of-plane bending of terminal methylene
f. Preparation of allobetulin (method A)
1. A llobetulin formate
1 part betulin and 8 parts formic acid ( 9 0 - 9 5 % ) are refluxed for 45
min; the solution turns violet. After cooling, it is filtered, and the solid
is extracted with ethanol and then crystallized from benzene; rhombic
crystals, mp 311-312°C.
2. Allobetulin
Allobetulin formate (4.5 g), 30 ml IN ethanolic potassium hydroxide,
and 5 ml benzene are refluxed for 30 min. Removal of the solvents
in vacuo leaves allobetulin, which is filtered and washed with a little
ethanol and water. Recrystallization from ethanol yields crystals of mp
260-261°C; yield, 3 g.
g. Preparation of allobetulin (method B)

Two g betulin in 10 ml chloroform and 5 ml hydrobromic acid (sp gr 1.39) are
refluxed for 1 hr. After distilling off the chloroform, the dark residue is
dissolved in ethanol, and water is added until the onset of turbidity. Recrys-
tallization from ethanol yields material of mp 260-261°C. [ a ] g + 48.25° (in
chloroform).
h. IR Spectrum of allobetulin (in KBr)

1
3425 c m " : Ο—H stretching

1380, 1370: gem-dimethyl
1140, 1040: C—Ο stretching of ring C—O—C
i. Allobetulin acetate
One g allobetulin and 10 g acetic anhydride are left overnight at room tem-
perature. The crystals are then filtered off and crystallized from ethanol as
plates of mp 275-276°. [ a ] g + 54.16° (in chloroform).
j. Oxyallobetulin acetate
To a boiling solution of 500 mg allobetulin acetate in 50 ml acetic acid is
slowly added 650 mg chromium trioxide in 45 ml acetic acid. After boiling
under reflux for 15 min, the mixture is cooled, diluted with water, and
extracted with chloroform. Distillation of chloroform leaves about 350 mg
which is dissolved in benzene, adsorbed on a column of 30 g alumina, and
eluted with benzene and benzene-ether. Oxyallobetulin acetate crystallizes as
plates of mp 360°C.
k. Oxyallobetulin
Oxyallobetulin acetate (300 mg) dissolved in 100 ml benzene, and 100 ml 5 %
ethanolic ( 9 5 % ) potassium hydroxide solution are refluxed for 1 hr. The
solution is concentrated in vacuo to half its volume, diluted with water, and
extracted with chloroform. The residue is crystallized as needles from etha-
nol. Mp 336-337°C; yield, 150 mg.
I. IR Spectrum of oxyallobetulin (in KBr)

1
3425 c m " : Ο—Η stretching
2920, 2850: C H 2 stretching
1765: C = 0 stretching of γ-lactone
1705: C = 0 stretching of δ-lactone
1215, 1190: two methyl groups attached to quaternary carbon atom
1255, 1120: C — O — C stretching of lactone
References
1. Hunefeld, J . (1836). Prakt. Chem. 7, 53.
2. Sosa, A . (1940). Ann. Chem. 14, 5.
3. Hirota, K . , Takano, T . , Taniguichi, K . , and Iguchi, K. (1944). J. Soc. Chem. Ind. Japan 47,
922.
4. Brunner, Ο., and Wohrl, R . (1934). Monatsh. Chem. 64, 2 1 .
5. Dieterle, H., Leonhardt, Η., and Dorner, Κ. (1933). Arch. Pharm. 271, 264.
6. Zimmermann, J . (1944). Helv. Chim. Acta 27, 332.
III. Terpenoids 217
7. Ruhemann, S., and Raud, H. (1932). Brennstoff Chem. 13, 341.

8. Ikan, R . , and McLean, J . (1960). / . Chem. Soc. 893.
9. Djerassi, C , Bowers, Α . , Burstein, S., Estrada, H., Grossman, J . , Herran, J . , Lemin, A.
J . , Manjarrez, Α . , and Pakrashi, S. C. (1956). / . Am. Chem. Soc. 78, 2312.
10. Schulze, Η., and Pieroh, K. (1922). Ber. 55, 2332.
11. Dischendorfer, O. (1923). Monatsh. Chem. 44, 123.
12. Davy, G. S., Halsall. T . G . , Jones, E . R . H., and Meakins, G. D . (1951). J. Chem. Soc.
2702.
Recommended Reviews
1. Barton, D . H. R . (1953). The chemistry of triterpenoids. In "Progress in Organic Chemistry"
J . W. Cook, (ed.), Vol. 2, p. 67. Butterworth, London.
2. Steiner, M., and Holtzem, H. (1955). Triterpene und triterpene saponine. In "Modern
Methods of Plant Analysis" (K. Paech, and M. V . Tracey, eds.), Vol. 3, p. 58. Springer-
Verlag, New York.
3. D e Mayo, P. (1963). Molecular rearrangements. In "Techniques of Organic Chemistry"
(K. W. Bentley, ed.), Vol. 11, part 2, p. 1087. Interscience, New York.
K. Isolation of Cerin and Friedelin from Cork

1. Introduction
Chevreul was the first to describe the cork alcohols cerin and friedelin (1).
The important fact that the sparingly soluble, crystalline material from cork
consists principally of at least two substances, which can be separated by a
series of recrystallizations from chloroform, was demonstrated by Istrati and
Ostrogovich (2). In honor of Friedel, Istrati named the more soluble sub-
stance friedelin.
Drake and Jacobsen (3) have isolated about 1.3% friedelin and 0 . Ι -
Ο. 15% cerin from cork. Friedelin was also isolated by Jefferies (4) from
Ceratopetalum apetalum, by Arthur, Lee, and Ma (5) from leaves of Rho-
dodendron westlandii, and by Weizmann, Meisels, and Mazur (6) from Citrus
paradisi.
HO
CH3 CH3
Cerin Friedelin
2. Principle
Ground cork is extracted with hot ethyl acetate. The filtrate contains cerin,
friedelin, and other constituents. On crystallization of cerin from chloroform,
friedelin is left in the mother liquor, which is concentrated and subjected
to column chromatography. Crystallization of friedelin from ethyl acetate
gives white needles. Both terpenes yield 2,4-DNP (dinitrophenylhydrazine)
derivatives.
3. Apparatus
4. Materials
Acetone Chloroform Ethyl acetate
Alumina Cork, ground Hydrochloric acid
Benzene 2,4-Dinitrophenylhydrazine Methyl cellosolve
5. Time
4 - 5 hours
6. Procedure
a. Isolation of cerin
To 75 g ground cork (20-30 mesh) in a 1-liter round-bottomed flask is added
500 ml ethyl acetate. The contents of the flask are heated on a water bath
under reflux for 3 hr, filtered on a Büchner funnel, and washed with 200 ml
hot ethyl acetate. The brown-colored filtrate is evaporated to dryness under
reduced pressure, and the residue obtained is crystallized twice from 3 to 5 ml
chloroform. Cerin is obtained in the form of silky needles, mp 255-256°C,
whereas friedelin is left in the mother liquor; yield, 50 mg.
IR Spectrum of cerin (in KBr)

- 1
3475 c m : Ο—Η stretching of secondary hydroxyl and intramolecular
hydrogen bond with C = 0
1710: C = 0 stretching, free
1650: bonded carbonyl
1380, 1360: gem-dimethyl group
1050: C—Ο stretching of alcoholic OH
III. Terpenoids 219
c. Cerin 2,4-dinitrophenylhydrazone
Cerin (50 mg) is dissolved in 5 ml hot methyl cellosolve, and 30 mg 2,4-
dinitrophenylhydrazine is added. The mixture is warmed until homogeneous.
One drop of concentrated hydrochloric acid is added, and the mixture is
boiled for 5 to 10 min. On cooling, the solution deposits orange-colored,
lath-like crystals, which are filtered off and recrystallized from a benzene-
alcohol mixture in the form of orange laths, decomposition point 253-255°C.
d. Isolation of friedelin
The chloroform filtrates from the first two recrystallizations of cerin are
evaporated under reduced pressure until solid separates from the hot solu-
tion. An equal volume of acetone is added, and the crude crystalline friedelin
is chromatographed over 5 g neutral alumina. Elution is started with a mix-
ture of benzene-chloroform, 9 : 1 , and the percentage of chloroform is grad-
ually increased. Recrystallization from ethyl acetate gives white needles of
friedelin melting at 262 to 263°C.
e. Friedelin
C NMR
13
f.
C-l 41.3 C-11 32.4 c •21 35.0
C-2 41.5 C-12 36.0 C •22 35.3
C-3 213.0 C-13 38.3 c •23 6.8
C-4 59.5 C-14 39.7 c •24 22.3
C-5 42.1 C-15 31.8 c •25 14.6
C-6 35.6 C-16 32.8 c -•26 17.9
C-7 30.5 C-17 30.0 c -•27 18.2
C-8 53.1 C-18 42.8 c -•28 20.3
C-9 37.4 C-19 39.2 c -•29 32.1
C-10 58.2 C-20 28.1 c -•30 18.6
g. Mass Spectrum
Friedelin C 3 oH 5 oO, Mol. wt. 426.
m/z 426(90%) 218(26%) 193(32%) 163(62%)
411(63%) 205(42%) 191(42%) 109(100%)
341(26%) 207(16%)
h. IR (in KBr)
- 1
3425 c m : Ο—H stretching
1715: C = 0 stretching, six-membered ketone
1110: aliphatic ketone
i. Friedelin 2,4-dinitrophenylhydrazone
Friedelin (50 mg) is dissolved in 5 ml hot methyl cellosolve, and 30 mg 2,4-
dinitrophenylhydrazine is added. The mixture is warmed until homoge-
neous. One drop concentrated hydrochloric acid is added, and the mixture
is boiled for 5 to 10 min. On cooling, the solution deposits orange-colored,
lath-like crystals which are recrystallized from benzene. The product melts
with decomposition at 297 to 299°C.
References
1. Chevreul. (1807). Ann. Chim. 62, 323.
2. Istrati, C , and Ostrogovich, . (1899). Compt. Rend. 128, 1581.
3. Drake, N. L . , and Jacobsen, R . P. (1935). J. Am Chem. Soc. 57, 1570.
4. Jefferies, P. R . (1954). J. Chem. Soc. 473.
5. Arthur, H. R . , L e e , C. M., and Ma, C. N. (1956). J. Chem. Soc. 1461.
6. Weizmann, Α . , Meisels, Α . , and Mazur, Y . (1955). J. Org. Chem. 20, 1173.
L. Removal of Bitter Components from Citrus Juices with

ß-Cyclodextrin Polymer
Limonin Nomilin
III. Terpenoids 221
HO OH
Naringin
1. Introduction
Limonoids are a group of chemically related triterpene derivatives found in
Rutaceae and Meliaceae families.
Limonin and nomilin are the major causes of juice bitterness, along with
the bitter-flavored naringin. In general, citrus juices contain limonoids at
levels below the bitterness threshold of 6 ppm. Intact fruits normally contain
a nonbitter precursor, limonoate Α-ring lactone, which differs from limonin
only in having a free carboxyl group at C-16 and a free hydroxyl group at
C-17. When the juice is extracted, this precursor lactonizes to the intensely
bitter dilactone, limonin, upon standing for a few hours under the juice's
acidic conditions (pH 3.5 to 4.5) or upon heating. The conversion is acceler-
ated by the enzyme limonin D-ring lactone hydrolase present in citrus.
It has been recently reported (1) that citrus tissues and juices contain
very high concentrations of limonoid glucosides, which are mildly bitter com-
pared to their limonoid aglycones.
Excessive bitterness stemming from the bitter principles such as limonin
and naringin in navel orange and grapefruit juice is an undesirable flavor
quality. Many attempts have been made to remove bitter components from
navel orange juice (2). Treatment of grapefruit juice with enzymes, such as
naringinaze, to hydrolyze the bitter glucoside naringin to the nonbitter agly-
cone, naringenin, has been reported by Kefford and Chandler (3).
Recently ion-exchange resins were used to remove titratable acids, as
well as limonin and naringin, from grapefruit juice. (4).
jß-Cyclodextrin monomer, which is soluble in aqueous solution, was
shown to decrease the bitter taste of limonin and naringin in citrus juice (5).
2. Principle
The following procedure (7) uses a- or /3-cyclodextrin polymer with commer-
cial citrus juices in a continuous fluid-bed or batch process to reduce levels
of limonin, nomilin, and naringin in the juices. The debittered juices are
evaluated by chromatographic (HPLC, T L C ) and by taste panel techniques.
It has been found (6)) that /3-cyclodextrin polymer reduced the levels of
limonin and naringin in citrus juice and that water or organic solvents re-
generated the polymer for use in debittering additional juice samples.
3. Apparatus
High-pressure liquid Chromatograph
Silica gel T L C plates
4. Materials
Acetic acid Ethanol
Acetone Ethyl ether
Benzene Grapefruit and orange concentrated juices
Chloroform Sodium borohydride
Cyclodextrin, a- or β Sodium hydroxide
Epichlorohydrin
5. Time
a. Overnight
b. 7 hours
6. Procedure
a. Preparation of Cyclodextrin polymers.
Navel oranges and grapefruit and frozen concentrated juices are purchased
at a local market. A mixture of a- or /3-cyclodextrin and 11 ml of water is
treated with a freshly mixed solution (80°C) of 13.5 g sodium hydroxide in
13.5 ml water. To the magnetically stirred mixture, 50 mg sodium borohy-
dride is added, followed by rapid, dropwise addition of 24 ml epichlorohy-
drin. The resulting pasty mixture undergoes a rapid, exothermic reaction is 10
to 20 min with brief, spontaneous refluxing, and a frothy, hard, glassy reac-
tion product is formed. The mixture is allowed to stand at room temperature
overnight and then heated to 50°C for 5 hr. If the spontaneous reflux fails to
occur, the mixture is heated to 60°C for 30 min. The glassy polymeric reaction
product is easily broken up and washed with acetone, 10 x 75 ml water (until
neutral), and 3 x 75 ml ethanol to remove water, and dried in air overnight to
yield 2 0 - 3 0 g polymer. The ethanol wash yields a dry polymer, easier to
handle than when the last wash is with water.
b. Batch process procedure for debittering

500 ml juice is stirred magnetically for 60 min with 10 g 2 0 - 6 0 mesh ß-
cyclodextrin polymer. The polymer is removed by filtration through a 60-
III. Terpenoids 223
2 0 0 ml/min. N 2 gas
Figure 3.6 Fluid-bed apparatus for debittering citrus juices.
mesh screen (Fig. 3.6) and regenerated by stirring the polymer for 30 min
each time with two or three 200 ml portions of 2 % sodium hydroxide solution
or absolute ethanol. Polymer, regenerated with dilute sodium hydroxide
solution, is then washed with 5 x 20 ml water and 2 x 50 ml ethanol and dried
in air before reuse.
c. Analytical Procedures
1. High-performance liquid chromatography (HPLC): Separations for
quantitation of naringin and naringenin 7/3-rutinoside in grapefruit
juice are carried out on a high-speed 5 μνη C-18 column, 12.5 cm long.
The eluting solvent is 2 0 % acetonitrile to 8 0 % water at 1.5 ml/min.
2. Thin-layer chromatography ( T L C ) is carried out on silica gel plates.
The developing solvent is benzene-chloroform-ether-acetic acid
(100:50:50:3).
The Rf value of limonin is 0.08 and of nomilin, 0.10.
d. Flavor tests
A taste panel may be used to compare the flavors of debittered navel orange
and grapefruit juices to those of the starting juices. Debittered grapefruit
juice may still have some of the bitterness expected of grapefruit juice, but at
a greatly reduced level, compared to the starting juice.
The debittering process with /3-cyclodextrin polymer does not adversely

affect the flavor of navel orange and grapefruit juices, nor does it decrease the
levels of major desirable components—sugars, acids, and ascorbic acid. The
decrease in the essential oil content due to the polymer treatment can be
corrected by addition of oil back to the juice.
References
1. Hasegawa, S. Bennett, D . , Herman, 2., Fong C. H., and Ou, P. (1989). Phytochem. 23,
1717.
2. Hasegawa, S., Patel, M. N., and Snyder, R. C. (1982). J. Agric. Food Chem. 30, 509.
3. Kefford, J . F . , and Chandler, Β . V . (1970). "The Chemical Constituents of Citrus Fruits,"
4. Johnson, R . L . , and Chandler, Β . V . (1982). J. Sei. Food Agric. 33, 287.
5. Konno, Α . , Misaki, M., Toda, J . , Wada, T , and Yasumatsu, K. (1982). Agric. Biol. Chem.
46, 2203.
6. Shaw, P. E . , and Wilson, C. W. / . Food Sei. 48, 646.
7. Shaw, P. E . , Tatum, J . H., and Wilson, C. W. (1984). J. Agric. Food Chem. 32, 832.
Recommended Review
1. Shaw, P. E . (1990). Cyclodextrin polymers in the removal of bitter compounds in citrus
juices. In "Bitterness in Foods and Beverages." ( R . Rouseff, ed.), pp. 3 0 9 - 3 2 4 . Elsevier,
Amsterdam, The Netherlands.
M. Questions
1. How are terpenes classified? Give an example of each class.

2. Write equations for the reactions you could expect to take place when
limonene is oxidized, reduced catalytically, treated with HBr.
3. What reagents and experimental conditions are required for the
reduction of thymol to menthol? How many stereoisomers can you
expect?
4. How can carvone be isolated from oil of caraway, and how can it be
synthesized?
5. What is the relationship of geraniol to nerol?
6. What products are formed by the action of ozone on ocimene,
limonene, and a-pinene?
7. Explain why dehydration of borneol with aqueous acid gives
camphene.
8. Show how /3-amyrin can be formed by cyclization of squalene.
9. Discuss the medicinal and industrial uses of terpenes.
10. Draw the structures of the following compounds and indicate the
isoprene units they contain: menthol, α-pinene, camphor, farnesol,
caryophyllene, abietic acid, and ß-amyrin.
III. Terpenoids 225
Ν. Recommended Books
1. Guenther, E . "The Essential Oils." Van Nostrand, New York.

2. Goodwin, T. W. (1971). "Aspects of Terpenoid Chemistry and
Biochemistry." Academic Press, New York.
3. De Mayo, P. (1959). "Mono- and Sesquiterpenoids." Interscience,
New York.
4. De Mayo, P. (1959). "The Higher Terpenoids." Interscience, New
York.
5. Pinder, A. R. (1960). "The Chemistry of the Terpenes." Chapman
and Hall, London.
6. Simonsen, J . L., and Owen, L. N. (1931). "The Terpenes, Vol. 1, The
Simpler Acyclic and Monocyclic Terpenes and Their Derivatives."
Cambridge University Press, New York.
7. Simonsen, J . L. (1932). Vol. 2, "The Bicyclic Terpenes, Sesquiterpenes,
and Their Derivatives " Cambridge University Press, New York.
8. Simonsen, J . L. and Barton, D. H. R. (1952). Vol. 3, The
Sesquiterpenes, Diterpenes, and Their Derivatives." Cambridge
University Press, New York.
9. Simonsen, J . L., and Ross, W. S. J . (1957). "Vols. 4 and 5, The
Triterpenes and Their Derivatives." Cambridge University Press,
New York.
NITROGENOUS / Λ \
COMPOUNDS
I. ALKALOIDS
A. Introduction
Alkaloids are nitrogenous compounds occurring in plants. Most of them

are optically active, and nearly all of them are of basic nature. Accordingly,
they very often form salts with plant acids such as quinic or meconic acid.
Some alkaloids are present in plants in combination with sugars (solanine),
while others occur as acid amides (piperine) or esters (cocaine, atropine). There
are certain exceptions to these general statements; thus, ricinine and col-
chicine are almost neutral compounds. Some alkaloids are quaternary salts
while others are tertiary amine oxides and therefore not basic.
The indole alkaloid, bufotenine, is found not only in plants (Piptadenia
pergrina), but also in toads (Bufo vulgaris) and fungi (Amanita mappa). In
general terms, the nitrogenous compounds found in fungi or other micro-
organisms should also be regarded as alkaloids, but this is not customary.
Other such compounds are: gliotoxin (fungus Trichoderma viride), pyocya-
nine (bacterium Pseudomonas aeruginosa), and erythromycin (strains of
Streptomyces).
The alkaloids found in the seeds, roots, and bark of plants are isolated
by extraction with dilute acids (hydrochloric, sulfuric, acetic) or alcohol. If
they are present as salts, they are liberated by treatment with calcium hydrox-
ide before extraction. The individual alkaloids are usually separated from the
very complex mixtures in which they occur by chromatographic methods.
Most alkaloids are colorless, crystalline compounds; a few, e.g., co-
niine, nicotine, and hygrine, are liquids, and some are colored, e.g., berber-
ine, which is yellow. Many alkaloids have a bitter taste and quite a number of
226
I. Alkaloids 227
them possess curative properties. For example, morphine has a narcotic

action, reserpine is a tranquilizer, atropine has an antispasmodic action,
cocaine is a local anesthetic, and strychnine is a nerve stimulant.
The function of alkaloids in plants is still a matter of controversy; they
are regarded as byproducts of plant metabolism, as reserve materials for
protein synthesis, as protective substances discouraging animal or insect
attacks, as plant stimulants or regulators similar to hormones, or simply as
detoxication products.
The presence of alkaloids is detected by either précipitants or color
reagents. The more important précipitants are those of Mayer, Wagner,
Dragendorff, and Bertrand. The color reagents mostly consist of dehydrating
or oxidizing agents or a combination of the two.
B. Method of Degradation
The most widely used process in degradative studies of alkaloids is exhaustive

methylation, known as Hofmann degradation, which involves the pyrolysis of
a quaternary ammonium hydroxide to form an olefin and a tertiary base.
C= C + :NR3 + H20
OH
When the nitrogen atom constitutes part of a ring, two degradations
must be carried out in order to ensure its complete removal. It should also be
borne in mind that when the exhaustive methylation of cyclic compounds
might be expected to give 1, 4-dienes, the alkaline conditions of the reaction
may result in the migration of one of the double bonds to give a 1, 3-diene,
e.g., the exhaustive methylation of N-methylpiperidine gives 1, 3-pentadiene
(piperylene) and not 1, 4-pentadiene.
CH3 H3C CH3 H 3C CH3

N-Methylpiperidine
Δ
II + N ( C H 3 ) 3 + H 2 0
OH"
Piperylene
H3C CH3
CH3
228 CHAPTER 4 Nitrogenous Compounds
The diene can then be easily hydrogenated to form a saturated hydro-

carbon.
In cases where the normal Hofmann degradation fails to bring about
ring fission of cyclic amines, the Emde degradation, involving catalytic re-
duction of a quaternary salt by sodium amalgam or sodium in liquid am-
monia, may be applied. For example, attempted Hofmann degradation of
iV-methyltetrahydroquinoline methohydroxide results in regeneration of the
parent base, while Emde reduction with sodium amalgam affords the ring-
opened amine.
A particular method of degradation is used in the case of alkaloids

having diphenyl ether linkages, e.g., the fe-benzylisoquinoline alkaloids.
They can be cleaved into two fragments by reduction with sodium in liquid
ammonia. Thus, the structure of the alkaloid dauricine was established by the
reductive cleavage of O-methyl-dauricine.
/-1 -(p-methoxy benzy l)-6,7-dimethoxy- M-(p-hydroxybenzyl)-6,7-dimethoxy-

2-methyl-1,2,3,4-tetrahydroisoquinoline 2-methyl-1,2,3,4-tetrahydroisoquinoline
I. Alkaloids 229
It should be mentioned that physical methods, in particular spectro-

scopic ( U V , I R , N M R , E S R , MS) methods and X-ray diffraction, are now
widely used in tackling structural and stereochemical problems relating to
such natural products.
The existing classification of alkaloids is based on a mixture of chemical
and botanical criteria. Thus, the pyrrolidine, pyridine, and indole alkaloids
are classified on the basis of their chemical structure. The Senecio alkaloids
on the other hand are so called because the genus Senecio provides the
greatest number of species containing alkaloids derived from a pyrrolizidine
moiety.
HO CH,OH
y ^ C H 2C O C H 3 T s r C H 2C H 2C H 3
Platynecine
CH3 H
(Pyrrolizidine group)
Hygrine Coniine
(Pyrrolidine group) (Pyridine group)
OH / - > y C H = C H 2
. C H 2N ( C H 3) 2
I
H OH
Gramine Cinchonine Vasicine
(Indole group) (Quinoline group) (Quinazoline group)
C H 3O
CH,0
CH,
HO
Solanidine
Papaverine (Steroid group)
(Isoquinoline group)
C H 2O H
H :
M
OCH,
Lupinine CH, OCH,
(Quinolizidine group)
Melicopicine
(Acridine group)
The structural types found in different classes of alkaloids are so diverse

that it is impossible to develop a single biogenetic hypothesis to include all
alkaloids.
Using tracer techniques, it has been shown that the heterocyclic nuclei
of many alkaloids are derived from only a limited number of amino acids,
e.g., ornithine, lysine, phenylalanine, and tryptophan, or products of their
breakdown.
The structural diversity of alkaloids in nature can be attributed mainly

to the involvement of C 3 , C 4 , and C 5 compounds such as acetone, acetoacetic
acid, and acetone dicarboxylic acid, the methylation of oxygen or nitrogen
atoms by the 5-methyl group of methionine, and the oxidative coupling of
phenols in the ortho and para positions of the phenyl.
C. Isolation of Caffeine from Tea

1. Introduction
Alkaloids having a purine nucleus form a small but important group of
natural products. They are often not classified as alkaloids because of their
almost universal distribution in living matter and their mode of biosynthesis,
which shows no relationship to amino acids from which most alkaloids arise.
Cafferine is one of the most important naturally occurring methyl deriv-
atives of xanthine. Its concentration in a variety of teas, including black and
green teas, depends both on climatic and topographic conditions of growth
and on processing methods, and was found to vary from 2.0 to 4 . 6 % . Thus,
Chinese black tea contains 2 . 6 - 3 . 6 % , Brazilian, 2 . 2 - 2 . 9 % , and Turkish,
2 . 1 - 4 . 6 % caffeine.
In addition to caffeine, other purines have also been reported to be
present in small quantities. Michl and Haberler (1) separated the following
compounds from black tea: caffeine, 2 . 5 % , theobromine, 0.17%, theophyl-
line, 0.013%, adenine, 0.014%, and traces of guanine, xanthine, and hypox-
anthine.
Caffeine was also isolated by Friese (2) from seeds of Genipa americana
(2.25%) and by Stenhouse (3) from coffee beans.
I. Alkaloids 231
Cola nitida is the principal source of kola nuts, which are important
because of their caffeine ( 3 - 5 % ) and theobromine contents.
Caffeine is used as a stimulant of the central nervous system. It has
myocardial and diuretic effects, and relaxes the smooth muscle of the bronchi.
Caffeine is a less potent diuretic than theobromine.
CH3
Caffeine
2. Principle
The experiment below involves the isolation of caffeine from tea leaves by
extraction with hot sodium carbonate solution, and neutralization and extrac-
tion with dichloromethane.
3. Apparatus
Sublimation apparatus
4. Materials
Sulfuric acid Dichloromethane
Tea Sodium carbonate
Celite
5. Time
4 - 5 hours
6. Procedure
Twenty g finely powdered tea leaves are placed in a 400 ml beaker, 5 g so-
dium carbonate and 100 ml water is added, and the mixture is heated by a
Bunsen burner for 20 min. Water is occasionally added to keep the volume
of the solution constant. The hot solution is then filtered, and the filtrate is
neutralized cautiously, with stirring, with sulfuric acid 1 0 % solution.
It is then filtered through a thin layer of a filter aid (Celite), placed on a
Büchner funnel padded with a wet filter paper, and washed with 20 ml di-
chloromethane. The two-phase filtrate is then placed in a separating funnel.
The organic lower layer is separated, and the aqueous layer is extracted twice
with two 40-ml portions of dichloromethane. The two organic (CH 2 C1 2 ) layers
are then combined, and the solvent is evaporated. Crude caffeine is crystal-
lized from a very small quantity of hot acetone or water. The pure crystalline
silky needles of caffeine (0.5 g) melt at 235°C.
a. Murexide test
A few crystals of caffeine and 3 drops of nitric acid are placed in a small
porcelain dish and evaporated to dryness. Addition of 2 drops of ammonium
hydroxide imparts a purple coloration.
b. Thin layer chromatography of xanthine derivatives

The crude tea extract is spotted on a thin-layer plate covered with Silica Gel
G F 2 5 .4 The developing solvent is chloroform-ethanol, 9.5:0.5. Detection:
(1) U V 2 5 4 n m — d a r k spots; (2) Iodine—HCl spray.
Solution A (prepared by dissolving 1 g potassium iodide and 2 g iodine
in 100 ml ethanol ( 9 6 % ) , is sprayed on the plate, followed (after 1 min) by
solution Β (prepared by mixing 5 ml ( 2 5 % HCl solution) with 5 ml ethanol
( 9 6 % ) . Theophylline yields a pink spot, R{ 0.1; theobromine, a violet spot,
R{ 0.2; and caffeine, yellow-brown spot, Rf 0.6.
c. IR spectrum of caffeine (solid film)

1
3134 c m " : C—H stretching
2850: Ν—CH 3 groups
1705: C = 0 stretching
1660: C = C stretching of tetrasubstituted double bond
1604, 1548, 1440: pyrimidine system
1470, 1358: asym. and sym. C H 3 bending
1230, 1197, 1020: C—Ν stretching
740: C—H deformation
d. UV spectrum of caffeine
water
λ max 278 τημ (loge 4.03)
Purines generally exhibit high-intensity selective absorption at 260 ιημ.
Substitution by alkyl groups causes a displacement to longer wavelengths.
e. NMR spectrum of caffeine
Position δ (ppm)
CH3 a 3.35
b 3.55
c 3.95
d 7.60
I. Alkaloids 233
f. Caffeine
CH;
13
g. C-NMR
C-l 30.4
C-3 32.3
C-7 35.8
h. Mass Spectrum
C 8 H 1 0 N 4 O 2 Mol. wt. 194
m/z 194 m/z 137 (M-CO)
m/z 165 (M-CH 3 ) m/z 109 (tropylium ion)
References
1. Michl, H., and Haberler, F . (1954). Monatsh. Chem. 35, 770.
2. Freise, F . W. (1935). Pharm. Zentr. 76, 704.
3. Stenhouse, J . (1854). Ann. 89, 244.
Recommended Reviews
1. Atta-ur-Rahman and Choudhary, M. I. (1990). Purine alkaloids. In "The Alkaloids,"
Vol. 38, ( A . Brossi, ed.), p. 225. Academic Press. New York.
2. Bokuchava, Μ. Α . , and Kobeleva, Ν. I. S. (1982). Tea aroma. In "Food Flavours, Part B . "
(I. D . Morton and A . J . Macleod eds.), p. 49, Elsevier, Amsterdam, The Netherlands.
3. Graham, H. (1983). Tea. In "Kirk-Othmer Encyclopedia of Chemical Technology,"
Vol. 2 2 , p. 628.
4. Stahl, W. H. (1962). The chemistry of tea and tea manufacturing. In "Advances in Food
Research" (C. O. Chichester, Ε . M. Mrak, and G . F. Stewart, eds.), Vol. 11, p. 202.
D. Isolation of Piperine from Black Pepper

1. Introduction
Piperine occurs in the unripe fruit (black pepper) and the kernel of the ripe
fruit (white pepper) of Piper nigrum and in the fruit of aschanti {Piper clusii).
It is also found in long pepper {Piper longum) (1) and in the seeds of Cubeba
censii (2). Piperine has also been isolated from Piper famechoni (3) and Piper
chaba (4).
The piperine content of black pepper varies from 6 to 9 % . Piperine is

tasteless, so some investigators have suggested that the stereoisomeric chavi-
cine, which accompanies piperine in the pepper, is possibly responsible for
the particular taste of pepper.
Piperine
2. Principle
In the following procedure, the piperine is extracted from black pepper
with ethanol and may be converted to a red TNB (1,3,5-trinitrobenzene)
complex.
Although piperine is tasteless at first, it does ultimately produce a
burning sensation and sharp aftertaste. The initial tastelessness of piperine
may be a consequence of its extremely low solubility in water. The crude
ethanol extract contains, in addition to piperine and chavicine (its geometric
isomer), some acidic, resinous material. In order to prevent co-precipitation
of piperine and the resin acids, dilute ethanol KOH solution is added to the
concentrated extract to keep acidic material in solution and/or as solid
gummy material that is precipitated in the vessel.
3. Apparatus
Soxhlet extractor
4. Materials
Black pepper Potassium hydroxide
Ethanol, 9 5 % 1,3,5-Trinitrobenzene
5. Time
3 hours
I. Alkaloids 235
6. Procedure
Ten g black pepper is ground to a fine powder and extracted with 150 ml 9 5 %
ethanol in a Soxhlet extractor for 2 hr. The solution is filtered and concen-
trated in vacuo on a water bath at 60°C. Alcoholic potassium hydroxide
(ten ml 1 0 % ) is added to the filtrate residue and after a while decanted from
the insoluble residue. The alcoholic solution is left overnight, whereupon yel-
low needles of mp 125-126°C are deposited; yield, 0.3 g.
Piperine forms a solid complex with 1,3,5-trinitrobenzene in a ratio 1:1,
in the form of red needles, mp 130°C.
a. Thin layer chromatography of black pepper extract

The crude extract is spotted on a thin-layer plate (Silica Gel G F 2 5 )4 and
developed with benzene-ethyl acetate, 2 : 1 . Detection: (1) U V 3 65 shows blue
fluorescence of piperine; (2) Spraying with anisaldehyde-sulfuric acid re-
agent, prepared by mixing anisaldehyde (0.5 ml) with glacial acetic acid
(10 ml), methanol (85 ml), and concentrated sulfuric acid (5 ml). This solu-
tion is sprayed on the plate, which is then heated at 110°C for 10 min. Piperine
appears as a yellow spot, R{ 0.25.
(c) (b)
1
b. H-NMR
δΗ 5.93 ( 2 Η , 7 ' ) , 7.40 ( 1 H , 3 ) , 6.43 ( 1 H , 2 ) , 3.57 ( 4 H , c ) , 1.62 (4h,6),
1.62 ( 4 H , a ) .
13
C NMR
C-l 164.5 C-2' 104.9
C-2 119.4 C-3' 147.4
C-3 141.6 C-4' 147.4
C-4 124.6 C-5' 107.6
C-5 137.3 C-6' 121.7
C - l ' 132.2 C-7' 100.6
d. M a s s spectrum
C 1 7 H 1 9 N 0 3 , Mol. wt. 285.
m/z 285(65%) 201(100%) 173(42%) 143(32%)
202(29%) 174(25%) 171(26%) 115(92%)
e. IR spectrum of piperine (in KBr disk)

- 1
3000 c m : aromatic C—H stretching
1635, 1608: sym. and asym. stretching of C = C (diene)
1608, 1580, 1495: aromatic stretching of C = C (phenyl ring)
1635: stretching of — C O — N c :
Methylenedioxy group:
2925, 2840: C H 2 asym. and sym. stretching, aliphatic C—H stretching
1450: C H 2 bending
1250, 1190: asym. stretching of = C — O — C
1030: sym. stretching of = C — O — C
930: most characteristic, probably related to C—Ο stretching
1132: in-plane bending of phenyl CH
995: C—H bending for trans — C H = C H —
850, 830, 805: out-of-plane C—H bending, 1,2,4-trisubstituted phenyl,
two adjacent hydrogen atoms.
f. UV spectrum of piperine
λ ™ 245 χημ (loge 4.47)
1-Phenylbutadiene in conjugation with — C O — R and methylenedioxy

chromophores.
References
1. Peinemann, (1896). Arch. Pharm. 234, 204.
2. Herlant, M. (1895). Chem. Zentr. 66, 319.
3. Barille, A. (1902). Compt. Rend. 134, 1512.
4. Bose, P. K. (1936). Chem. Zentr. 107, 4315.
Recommended Review
1. Marion, L. (1950). The pyridine alkaloids. In "The Alkaloids," ( R . H. F . Manske, and H. L.
Holmes, eds.), Vol. 1, p. 167. Academic Press, New York.
E. Degradation of Piperine
1. Introduction
As early as 1849, piperine was hydrolyzed with aqueous sodium hydroxide
(1), and later with nitric acid ( 2 ) , to yield a volatile base, piperidine, and
piperic acid (3). Spring and Stark [4] used ethanolic potassium hydroxide for
hydrolysis of piperine. The presence of two double bonds in piperic acid was
proved by its catalytic reduction to tetrahydropiperic acid and by the prepa-
ration of tetrabromopiperic acid by bromination with bromine in carbon
I. Alkaloids 237
I
COCH
I Ο—CH, KOH
HC-CH CH,OH
II
HC
Piperine
HOOC-CH
II Ο—CH,
HC—CH
II
+ HC
Ν
I
Piperic acid
Η
Piperidine
disulfide. The structure of piperic acid was deduced from its oxidation by
potassium permanganate to yield oxalic acid, piperonal, and piperonylic acid.
HOOC-CH
II KMn04
HC—CH
HC-^ V
Piperic acid
COOH / O ^ ^ ^ C H O X k ^ r O O H
ι +
COOH
Ό
Oxalic acid
Piperonal Piperonylic acid
Mild oxidation ( K M n 0 4 in basic solution) yields piperonal, piperonylic acid,

and tartaric acid.
Piperine can be synthesized from the chloride of piperic acid and piper-
idine.
2. Principle
In the following degradation, piperine is treated with ethanolic potassium
hydroxide, yielding piperic acid and piperidine (isolated as the hydro-
chloride).
3. Apparatus
4. Materials
Ethanol, 9 5 % Piperine
Hydrochloric acid Potassium hydroxide
5. Time
3 hours
6. Procedure
Piperine (1 g) and 10 ml 10% alcoholic potassium hydroxide are refluxed for
90 min. The ethanolic solution is evaporated to dryness under reduced pres-
sure, the receiver being cooled in an ice-salt bath. The solid potassium
piperinate is suspended in hot water and acidified with hydrochloric acid. The
voluminous yellow precipitate is collected on a Büchner funnel, washed with
cold water, and recrystallized from ethanol to yield piperic acid as yellow
needles of mp 216-217°C. The strongly basic ethanolic distillate in the re-
ceiver is saturated with hydrochloric acid and evaporated to dryness to give
piperidine hydrochloride, which melts at 244°C after recrystallization from
ethanol.
References
1. Wortheim, T . (1849). Ann. 7 0 , 58.
2. Anderson, T . (1850). Ann. 7 5 , 80.
3. Strecker, A . (1858). Ann. 1 0 5 , 317.
4. Spring, F . S., and Stark, J . (1950). J. Chem. Soc. 1177.
Recommended Review
1. Marion, L. (1950). The pyridine alkaloids. In "The Alkaloids" ( R . H. F. Manske, and H. L.
Holmes eds.), Vol. 1, p. 167. Academic Press, New York.
F. Isolation of Strychnine and Brucine from the Seeds of Strychnos

nux vomica
1. Introduction
Strychnine, C 2 i H 2 2 0 2 N 2 , and brucine, C23H26O4N2, were first isolated by
Pelletier and Caventou in 1819 from the seeds and bark of Strychnos nux
vomica. Nux vomica seeds contain about 3 % alkaloids, of which a little more
I. Alkaloids 239
than half is made up of strychnine, the other alkaloids being brucine, col-
ubrine, vomicine, and pseudostrychnine. In recent years it was found that
Australian (1) and Congolese (2) Strychnos species also contain strychnine,
brucine, and other alkaloids.
Strychnine is intensely bitter; one part of strychnine is capable of im-
parting a bitter taste to 500,000 parts of water. It is a virulent poison and is
used medicinally as a tonic and stimulant.
Brucine is even bitterer than strychnine. Its uses are similar to those of
strychnine but its action is so much milder that it is used on a very large scale
for denaturation of ethanol.
Strychnine Brucine
2. Principle
In the following procedure, a mixture of strychnine and brucine is extracted
with chloroform from the crushed nuts, which have been treated overnight
with calcium hydroxide. Crystallization of the crude mixture from 5 0 % etha-
nol yields crystalline strychnine, which is converted to its sulfate. Brucine
(which is more soluble in alcohol) is recovered from the mother liquor, also as
the sulfate.
Apparatus
Soxhlet extractor
Materials
Acetone Ethanol, 9 5 % Sodium carbonate
Acetic acid, glacial Nitric acid Sodium hydroxide
Calcium hydroxide Nux vomica seeds Sulfuric acid
Chloroform Potassium dichromate
5. Time
Treatment of seeds with calcium hydroxide: 12 hours
Isolation of strychnine and brucine: 4 - 5 hours
6. Procedure
Groundnuts (200 g) are mixed thoroughly with 200 ml suspension of 10%
calcium hydroxide in water and left overnight at room temperature. After
air drying, the slurry is extracted with chloroform in a Soxhlet extractor for
3 hr. The chloroform solution is then extracted several times with 5 % sulfuric
acid solution, and subsequently basified with 10% aqueous sodium hy-
droxide. After cooling, the crystals are filtered, 1.5 volumes of 5 0 % ethanol
are added, and the mixture is refluxed until most of the solid has dissolved.
After addition of a little activated charcoal, the solution is filtered hot and left
overnight. The crystals of strychnine are filtered and washed with a little
5 0 % ethanol. The mother liquor and washings are kept for the isolation of
brucine.
a. Preparation of strychnine sulfate

The crude strychnine is dissolved in 9 volumes of boiling water, and 1 5 %
sulfuric acid solution is added slowly, with stirring, until the reaction is
slightly acid to Congo red. Activated charcoal is added and the solution is
refluxed for 1 hr and filtered hot. The sulfate, which crystallizes on cooling,
is filtered and washed with cold water.
b. Pure strychnine
Strychnine sulfate is dissolved in 15 volumes of water at 80°C and neutralized
with 10% aqueous sodium carbonate; after addition of charcoal, the solu-
tion is filtered hot. Strychnine precipitates on addition of aqueous sodium
carbonate and cooling. The precipitate is filtered on a Büchner funnel and
washed with cold water. Recrystallization from ethanol yields a product of
mp 286-288°C.
c. Strychnine
13
d. C NMR
C-2 60.1 C-5 50.2 C-7 51.9
a
C-3 60.1 C-6 42.S C-8 132.6
I. Alkaloids 241
C-9 122.3 C-14 26.8 C-19 127.7

C-10 124.3 C-15 31.5 C-20 140.3
C-11 128.6 C-16 48.2 C-21 52.7
C-12 116.2 C-17 77.5 C-22 42.3"
C-13 142.2 C-18 64.6 C-23 169.4
a
Shifts may be interchanged.
e. Mass Spectrum
C 2 1 H 2 2 N 2 0 2 , Mol. wt. 334.
m/z 334(100%) 120(37%) 77(35%) 44(44%)
144(32%)) 107(33%) 55(33%) 41(34%)
f. UV Spectrum of strychnine
H
AmS 240 τημ (loge 4.15); 270(3.92); 294(3.72).
The U V absorption spectrum of strychnine closely resembles that of
hexahydrocarbazole, as the formula might have led us to expect.
g. Brucine sulfate
The mother liquor remaining after strychnine separation is concentrated in
vacuo on a water bath until most of the alcohol has been removed. The
residue is acidified to pH 6 with dilute sulfuric acid and then concentrated to a
volume of 3 to 4 ml. After standing in a refrigerator overnight, the product is
filtered and washed with cold water. Brucine sulfate is purified by dissolution
in 4.5 volumes of hot distilled water and boiled with a little charcoal for 1 hr.
It is filtered hot and left in a refrigerator for several days. Brucine is recovered
from the sulfate in a manner analogous to that outlined for strychnine;
recrystallization from aqueous acetone yields crystals of mp 178°C.
Warning! Extreme caution should be exercised in carrying out this
experiment. The hands must be washed thoroughly because of the high
toxicity of these alkaloids.
h. Brucine
1
i. H NMR
a. 1.15-3.70 (11H) f. 4.12 2H
b. 2.04 2H g. 4.30 1H
c. 3.82 1H h. 5.91 1H
d. 3.88 3H i. 6.69 1H
e. 3.92 3H j. 7.83 1H
13
j. C NMR
C-2 60.3 C - l l 149.3 C-19 127.2
C-3 59.9 C-12 101.1 C-20 140.6
C-5 50.1 C-13 136.0 C-21 52.7
C-6 42.3 C-14 26.8 C-22 42.3
C-7 51.9 C-15 31.5 C-23 168.9
C-8 123.6 C-16 48.3 OMe 56.2
C-9 105.7 C-17 77.8 OMe 56.4
C-10 146.2 C-18 64.6
References
1. Anet, F. A . L . , Hughes, G. K . , and Ritchie, E . (1953). Australian J. Chem. 6, 58.
2. Jaminet, F . (1953). J. Pharm. Belg. 8, 339.
Recommended Reviews
1. Cromwell, Β . T . (1955). Alkaloids of Strychnos spp. In "Modern Methods of Plant Analysis, "
(K. Paech, and M. V . Tracey, eds.), Vol. 4, p. 480. Springer-Verlag, New York.
2. Robinson, R . (1952). Molecular structure of strychnine, brucine, and vomicine. In "Progress
in Organic Chemistry," ( J . W. Cook, ed.), Vol. 1, p. 1. Butterworth, London, England.
G. Synthesis of Mescaline
1. Introduction
Mescaline, an active hallucinogen, was first synthesized in 1919 by Spath,
who used 3,4,5-trimethoxybenzoyl chloride as his starting material (1). Sub-
I. Alkaloids 243
sequently, a number of improved syntheses have been reported. Slotta and

Heller (2) prepared mescaline by Hofmann degradation of trimethoxyphen-
ylpropionamide, and Kinder and Peschke (3) by condensation of 3,4,5-tri-
methoxybenzaldehyde with potassium cyanide, acetylation, and catalytic re-
duction.
Hahn and Wassmuth (4) used elemicine as their starting material, and
Hahn and Rumpf (5) later described the preparation of mescaline by catalytic
reduction of ω-nitrotrimethoxystyrene. Benington and Morin (6) reduced
3,4,5-trimethoxy-jß-nitrostyrene with lithium aluminum hydride and obtained
an 8 6 % yield of mescaline.
The most striking physiological affect of mescaline is the production of
visual color hallucinations, which can be induced by doses of 0.3 to 0.4 g
mescaline sulfate. Auditory, gustatory, and other sensory hallucinations have
also been recorded.
COOH COOH
3 ( C H 3) 2S 0 4 ( C H 3) 2S 0 4
CH.O OCH,
OCH,
Trimethoxybenzoic acid
COOCH, C H 2O H
LiAlH 4 Γ il HCl
CH.O OCH3 CH3(K^ÔCH 3
OCH3 OCH3
Methyl-3A5-trimethoxybenzoate 3,4,5-Trimethoxybenzyl alcohol
CH 2 C1 C H 2C N
CH3O^YÔCH
CHjCT^YÔCHj 3
0CH3 OCH3
3,4,5-Trimethoxybenzyl chloride 3,4,5-Trimethoxyphenyl acetonitrile
C H 2C H 2N H 2
CH3O X)CH3
OCH3
Mescaline
2. Principle
The synthesis (7, 8) of mescaline involves the following stages: gallic acid—»
3,4,5-trimethoxybenzoic acid—» methyl ester of trimethoxybenzoic acid—»
3,4,5-trimethoxybenzyl a l c o h o l s 3,4,5-trimethoxybenzyl chloride-*3,4,5-
trimethoxyphenyl acetonitrile^ mescaline.
3. Apparatus
Reflux assembly
4. Materials
Dimethyl sulfate Potassium cyanide
Dry ether Picric acid
Ether Potassium hydroxide
Gallic acid Sodium carbonate
Hydrochloric acid Sodium sulfate, anhydrous
Lithium aluminum hydride Sulfuric acid
5. Time
9 - 1 0 hours
6. Procedure
a. 3,4,5,-Trimethoxybenzoic acid
To a cold solution of 80 g sodium hydroxide in 500 ml water in a 1-liter flask is
added 50 g gallic acid. The flask is immediately tightly stoppered, and the
mixture is shaken occasionally until all the acid has dissolved. Dimethyl
1
sulfate 89 g (67 ml) is then added and the flask is shaken for 20 min while
being cooled by means of cold water in order to ensure that the temperature
does not rise above 30 to 35°C. Occasionally the stopper is raised to release
any built-up pressure. A second portion of 89 g dimethyl sulfate is then
added, and shaking is continued for an additional 10 min. During this second
addition, the temperature may rise to 40 to 45°C. The flask is then fitted with
a reflux condenser, and the contents are boiled for 2 hr. In order to saponify
the small amount of ester produced, a solution of 20 g sodium hydroxide in
30 ml water is then added, and boiling is continued for 2 additional hr. The
' T h e toxic nature of methyl sulfate must always be borne in mind! Ammonia is a specific
antidote for methyl sulfate and should be kept at hand to destroy any of the ester
accidentally spilled.
I. Alkaloids 245
reaction mixture is then cooled and acidified with dilute hydrochloric acid.
The precipitated trimethoxybenzoic acid is filtered with suction and washed
well with cold water. The product melts at 157 to 160°C and weighs 5 0 - 5 2 g.
It may be purified by recrystallization from 2 liters boiling water with the use
of decolorizing carbon, the filtration being carried out in a steam-jacketed
funnel. In this way, 4 1 - 4 3 g colorless needles melting at 167°C are obtained.
b. Methyl ester of 3,4,5-trimethoxybenzoic acid

To a solution prepared from 50 g 3,4,5-trimethoxybenzoic acid, 10 g sodium
hydroxide, 27 g sodium carbonate, and 300 ml water are added, with stirring,
47 ml methyl sulfate during the course of 20 min. The reaction mixture is
refluxed for half an hour. The crude ester (33 g) precipitates from the cold
mixture. From the filtrate 19 g of starting material are recovered upon acid-
ification with dilute hydrochloric acid. The ester is further purified by
dissolving it in the minimal amount of methanol and treatment with Norit.
Usually it is necessary to repeat this treatment to obtain a colorless crystalline
product that melts at 80 to 82°C.
c. 3,4,5-Trimethoxybenzyl alcohol
To a suspension of 6.9 g lithium aluminum hydride in 300 ml anhydrous ether
is added, in the course of 30 min, a solution of 34 g methyl ester of 3 , 4 , 5 -
trimethoxy-benzoic acid in 450 ml ether. The solid that forms is carefully
decomposed with 75 ml ice water. After décantation of the ether, 375 ml
ice-cold 1 0 % sulfuric acid is added. The product is extracted with 200 ml
ether. After drying over sodium sulfate, the combined extracts are freed of
ether, and the residue is distilled. Bp 135-137°C (0.25 mm); yield 22 g ( 7 3 % ) .
d. 3,4,5-Trimethoxybenzyl chloride
A mixture of 20 g 3,4,5-trimethoxybenzyl alcohol and 100 ml ice-cold con-
centrated hydrochloric acid is shaken vigorously until a homogeneous solu-
tion is obtained. Within a few minutes a turbidity develops, followed by heavy
precipitation of a gummy product. After 3 hr and dilution with 100 ml ice
water, the aqueous layer is decanted and extracted with three 60-ml portions
of benzene. The gummy organic residue is then dissolved in the combined
benzene extracts. The benzene solution is washed with water and dried over
sodium sulfate. It is then transferred to a distilling flask, and the benzene is
removed under reduced pressure. The red, semisolid residue is suspended in
a small amount of ice-cold ether and filtered through a chilled funnel. The
crystalline product, after washing with small portions of cold ether, weighs
7.8 g. After standing in a refrigerator, the combined filtrates yield more
crystals. The total yield is 10.5 g ( 4 8 % ) . After four recrystallizations from
benzene, colorless needles are obtained, mp 60-62°C.
e. 3,4,5-Trimethoxyphenyl acetonitrile
A mixture of 9 g potassium cyanide in 35 ml water, 60 ml methanol, and 9.7 g
3,4,5-trimethoxybenzyl chloride is heated for 10 min at 90°C. The solvents
are partially removed under reduced pressure. The residue is then extracted
with 90 ml ether in three portions. The combined extracts are washed and
dried over sodium sulfate. After removal of the drying agent, the ether
solution is warmed on a steam bath, and the ether is removed by a stream of
air. On chilling, the residue yields scale-like crystals. Recrystallization from
ether gives rectangular prisms: yield 2.5 g ( 2 7 % ) ; mp 76-77°C.
f. Mescaline
In 150 ml anhydrous ether is suspended 0.85 g lithium aluminum hydride
powder. Two grams of 3,4,5-trimethoxyphenyl acetonitrile in 150 ml an-
hydrous ether are added, with stirring, during the course of 15 min. After
stirring for an additional 15 min, 10 ml ice water is introduced carefully. A
mixture of 10 g sulfuric acid in 40 ml water is then added at a moderate rate.
The aqueous layer is separated and treated with concentrated sodium hydrox-
ide. The brown oil is extracted with three 30-ml portions of ether. The
combined extracts are washed once with water and dried over potassium
hydroxide pellets. To the decanted ether solution is added a mixture of 1 g
sulfuric acid and 25 ml ether. The white precipitate is washed several times
with ether; yield, 1.2 g ( 4 0 % ) . After two recrystallizations from 9 5 % ethanol,
the colorless, long, thin plates soften at 172°C and melt at 183°C. The picrate
prepared from the acid sulfate melts at 217°C (dec.) after triple recrystalliza-
tion from ethanol. The chloroplatinate prepared from the free base melts at
184 to 185°C.
g. UV spectrum of mescaline sulfate
A ™ 264,266,269 ταμ.
The spectrum is similar to that of phenylethylamine sulfate, but shows a
bathochromic shift obviously due to the presence of the methoxyl group in
the benzene ring, especially that in the para position.
h. Mass Spectrum
Mescaline C n H 1 7 N 0 3 Mol. wt. 211.
m/z 211(17%) 182(59%) 167(25%) 44(100%)
183(7%) 181(34%) 151(6%) 30(70%)
References
1. Spath, Ε . (1919). Monatsh. Chem. 40, 129.
2. Slotta, Κ. H., and Heller, H. (1930). Ber. 63, 3029.
I. Alkaloids 247
3. Kindler, Κ . , and Peschke, W. (1932). Arch. Pharm. 270, 410.

4. Hahn, G . , and Wassmuth, H. (1934). Ber, 67, 696.
5. Hahn, G . , and Rumpf, F . (1938). Ber. 7 1 , 2141.
6. Benington, F . , and Morin, R . D . (1951). / . Am. Chem. Soc. 73, 1353.
7. Tsao, M. U . (1951). J. Am. Chem. Soc. 73, 5495.
8. Donrow, Α . , and Petsch, (1952). Arch. Pharm. 285, 323.
Recommended Review
1. Reti, L . , (1953). ß-Phenylethylamines. In "The Alkaloids," ( R . H. F . Manske, and H. L.
Holmes eds.), Vol. 3, p. 313. Academic Press, New York.
H. Gas Chromatography of Alkaloids

I. Introduction
In 1958, Quin (1) used gas-liquid chromatography to study the alkaloidal
composition of tobacco smoke. More recently, Lloyd and coworkers (2)
have shown that a large number of alkaloids, even those of high molecular
weight, can be successfully separated by gas chromatography if a suitable
stationary phase is used.
Nonpolar silicone polymers, particularly silicone rubber S E - 3 0 , possess
great thermal stability and have been used successfully for gas chromatogra-
phy of alkaloids ( 3 - 6 ) . However, polar liquid phases often have distinct
advantages over nonpolar phases. Because of greater solute-solvent interac-
tion, they are more selective and may often effect separation of substances
that do not separate on non-polar columns.
2. Principle
The following experiment (7) uses a nonpolar silicone polymer ( S E - 3 0 ) and a
moderately polar cyanosilicone ( X E - 6 0 ) . Because of its high selectivity, the
latter appears to be the stationary liquid of choice for most alkaloid separa-
tions. Thus, atropine and scopolamine, morphine, codeine, and thebaine,
quinine and quinidine, as well as cinchonine and cinchonidine, are readily
separated on the more polar stationary phase ( X E - 6 0 ) .
3. Apparatus
Gas-chromatograph
Microsyringe
Spiral glass column
4. Materials
Atropine Hydrastine
Caffeine Morphine
Chloroform Narcotine
Cinchonidine Papaverine
Cinchonine Pilocarpine
Cocaine Quinidine
Codeine Quinine
Cyanosilicone X E - 6 0 Scopolamine
Gas Chrom Ρ Silicone polymer S E - 3 0
Hexamethyldisilazane Strychnine
Homatropine Thebaine
5. Time
4 hours
6. Procedure
a. Preparation of column
A spiral glass column 3 ft long and with an internal diameter of 0.07 in is
used. The solid support is Gas Chrom Ρ, 8 0 - 1 0 0 mesh, which is washed with
concentrated hydrochloric acid and deactivated by treatment with 5 % hexa-
methyldisilazane in toluene for 10 min. The silanized support is then filtered
on a Büchner funnel, washed with toluene, and coated with 1% stationary
liquid ( S E - 3 0 or X E - 6 0 ) in toluene. The support is then refiltered and dried
at 80°C for 2 hr. Columns are packed by gradual addition of the coated
support accompanied by repeated tapping.
b. Preparation of samples
The alkaloids are dissolved in analytical grade acetone or chloroform to give
a concentration of 0.5 to 1% and introduced with a Hamilton microsyringe.
The columns are operated at optimal flow rates. The temperature of the
injection port should be about 300°C.
The following table summarizes the retention values of the alkaloids on
two stationary phases at three different temperatures.
I. Alkaloids 249
Relative Retention Values of Alkaloids
SE-30 ( 1 % ) XE-60 ( 1 % )
Alkaloid 175° 225° 220°
Atropine 0.51 — 0.59

Caffeine 0.15 — 0.32
Cinchonidine — 2.12 3.28
Cinchonine — 2.06 3.04
Cocaine 0.52 — 0.48
0
Codeine 1.00 1.00 1.00
Homatropine 0.31 — 0.39
Hydrastine — 5.95 17.70
Morphine — 1.26 2.71
Narcotine — 11.60 20.70
Papaverine — 3.59 6.63
Pilocarpine 0.40 — 2.20
Quinidine — 3.41 6.63
Quinine — 3.41 6.95
Scopolamine 0.84 — 1.40
Strychnine — 6.89 14.70
Thebaine — 1.55 1.54
a
Codeine is used as the standard for calculation of
relative retention values; it is arbitrarily given the
value 1.00. Its actual retention times are 16.4 min
(175°C), 1.7 min (225°C), and 3.6 min (220°C).
References
1. Quin, L . D . (1958). Nature 182, 865.
2. Lloyd, Η. Α . , Fales, Η. M., Highet, P. F . , Vanden Heuvel, W. J . Α . , and Wildman, W. C.
(1960). J. Am. Chem. Soc. 82, 3791.
3. Brochmann-Hanssen, E . , and Svendsen, A . B . (1962). / . Pharm. Sei. 5 1 , 1095.
4. Parker, K. D . , Fontan, C. R . , and Kirk, P. L. (1963). Anal. Chem. 35, 346.
5. Arndt, R . R . , Baarschers, W. H., Douglas, B . , Shoop, E . C , and Weisbach, J . A . (1963).
Chem. Ind. (London) 1163.
6. Mule, S. J . (1964). Anal. Chem. 3 6 , 1907.
7. Brochmann-Hanssen, E . , and Fontan, C. R . (1965). / . Chromatogr. 19, 296.
Recommended Review
1. Burchfield H. P., and Storrs, Ε . E . (1962). Chromatography of alkaloids. In "Biochemical
Applications of Gas Chromatography." p. 366. Academic Press, New York.
I. Thin-Layer Chromatography of Opium Alkaloids

1. Introduction
Many investigators failed to group the alkaloids in one analytical system
because of the great variety of ring systems and their differing basicities.
Opium alkaloids were first separated on thin layers by Borke and Kirch (1) in
1953. Machata (2), Baumler and Rippstein (3), Bayer (4), and Steele (5) have
used silica gel G for the same purpose. Tiechert, Mutschler and Rochelmeyer
(6) reported the separation of opium alkaloids using layers of alkaline silica
gel G. Winkler and Awe (7) and Ikram, Niana, and Islam (8) separated
opium alkaloids on thin layers of alumina G.
Most alkaloids are detected by observation of the fluorescence under
ultraviolet light and by spraying with reagents such as Dragendorff, eerie
sulfate, and iodo-platinic acid.
2. Principle
Thin-layer chromatography is preeminently suitable as a rapid method for
screening plants for alkaloid content.
3. Apparatus
T L C applicator
Glass plates (20 x 20 cm)
Spray gun
4. Materials
Acetone Methanol Potassium iodide
Bismuth subnitrate Methyl ethyl ketone Silica gel G
Chloroform Morphine Tartaric acid
Codeine Narcotine Thebaine
Diethylamine Papaverine Xylene
5. Time
2 - 3 hours
6. Procedure
gel G and 50 ml water for 30 sec; it is then spread on the plates with an
applicator to give a layer of 0.25 mm thickness. After 30 min at room
temperature, the plates are activated in an oven at 120°C for 30 min.
I. Alkaloids 251
b. Development
The samples of the alkaloids are dissolved in chloroform and spotted by
means of micropipettes along a line 2 cm above the rim of the plate. Develop-
ment is carried out in either of the following two solvent systems: (1) chloro-
form-acetone-diethylamine, 5 : 4 : 1 ; (2) xylene-methyl ethyl ketone-
methanol-diethylamine, 2 0 : 2 0 : 3 : 1 .
c. Detection
The dried plates are first examined under ultraviolet light and then sprayed
with a modified Dragendorff's reagent which is a mixture of the following two
solutions: (1) 17 g bismuth subnitrate and 200 g tartaric acid in 800 ml water;
(2) 160 g potassium iodide in 400 ml water.
Retention Characteristics of Alkaloids
Rf in Solvent System
Alkaloid 1 2
Morphine 0.10 0.12

Codeine 0.38 0.26
Thebaine 0.65 0.45
Papaverine 0.67 0.59
Narcotine 0.72 0.74
References
1. B o r k e , Ν. L . , and Kirch, E . R . (1953). J. Am. Pharm. Assoc., Sei. Edit. 42, 627.
2. Machata, G . (1960). Mikrochim. Acta. 79.
3. Baumler, J . , and Rippstein, S. (1961). Pharm. Acta Helv. 36, 382.
4. Bayer, J . (1964). J. Chromatogr., 16, 237.
5. Steele, J . A . (1965). J. Chromatogr., 19, 300.
6. Teichert, K . , Mutschier, E . and Rochelmeyer, H. (1960). Deut. Apotheker Ztg., 100, 283.
7. Winkler, W . , and Awe, W. (1961). Arch. Pharm. 294, 301.
8. Ikram, M., Miana, G. Α . , and Islam, M. (1963). J. Chromatogr. 11, 263.
Recommended Review
1. Waldi, D . Alkaloids. In Stahl, E . 'Thin-layer Chromatography," p. 279. Academic Press,
New York. (1965).
J. Questions
1. What initial steps would you take to establish the structure of an

unknown natural alkaloid?
2. How are alkaloids distinguished from proteins? What is the biogenetic

relationship between the two groups of compounds?
3. Why is tannic acid used as an antidote in cases of poisoning by
alkaloids?
4. List six heterocyclic structures that constitute the basis of important
alkaloids. Indicate an alkaloid derived from each.
5. Many alkaloids, e.g., quinine, strychnine, and brucine, are used in
the resolution of racemic mixtures of optically active acids. Explain
the reason for this method and describe in detail how you could
resolve racemic mandelic acid.
6. Write equations illustrating Hofmann's exhaustive methylation of
coniine ( I ) , lobelanine ( I I ) , and papaverine (III).
7. Which products are obtained when nicotine is (a) reduced by sodium

in ethanol; (b) oxidized by nitric acid?
8. When cigarette smoke is blown through a white handkerchief, a stain
is left. Is this stain due to nicotine? Explain.
9. Capsaicin, the alkaloid from red pepper, has the following structure:
C H 2N H C O ( C H 2) 4C H = C H C H ( C H 3) 2
By which reactions could you prove this formula?

II. Amino Acids 253
2
10. How can nicotine (I) and papaverine (II) be synthesized?
C H 3C X ^
CH30
CH3
OCH3
OCH3
11. Cusparine, C 1 9 H 1 7 N 0 3 (from Angostura bark), gives

4-methoxy-quinoline-2-carboxylic acid and piperonylic acid
(3,4-methylenedioxy-benzoic acid) on oxidation with potassium
permanganate. Suggest a structure for cusparine.
12. How are the following alkaloids interrelated chemically: morphine,
codeine, heroine, and apomorphine?
13. Write equations for the synthesis of tropinone by Robinson's method.
Why is this synthesis (like many similar ones) termed synthesis under
physiological conditions?
14. What are the sources and structures of uric acid, theophylline,
theobromine, and caffeine?
15. What is the pathway of biosynthesis of the following alkaloids:
papaverine, harmane, mescaline?
K. Recommended Books
1. Bentley, K. W. (1957). "The Alkaloids, Parts 1-2." Interscience, New

York.
2. Bernfeld, P. (1963). "Biogenesis of Natural Products." Pergamon
Press, London, England.
3. Hendrickson, J . B . (1965). "The Molecules of Nature." Benjamin,
New York.
4. Manske, R . H. F. (1960-1977). "The Alkaloids." 16 Volumes.
II. AMINO ACIDS

A. Introduction
The amino acids are colorless crystalline compounds that are generally solu-
ble in water, but sparingly soluble in organic solvents. They are amphoteric
compounds, their reactions with acids and bases being given by the following
equation:
N H 3- C H R - C O O H N H 3- C H R - C O O N H 2- C H R - C O O + H20
However, they are normally written in their classical form R C H - N H 2 -

COOH. If R is a group other than hydrogen, the acid will have an asymmet-
ric carbon atom, and can therefore occur in an optically active form. The
isomers having the L-configuration are most widely distributed in nature.
For each amino acid in solution there is a characteristic pH value at
which it exists only in the zwitterion form. This pH is known as the isoelectric
point. At this point the amino acid has its lowest solubility.
The amino acids are classified as follows:
aliphatic neutral, such as glycine, C H 2 ( N H 2 ) C O O H
aliphatic acidic, such as aspartic acid, H O O C - C H 2 - C H ( N H 2 ) - C O O H
aliphatic basic, such as lysine, N H 2 - ( C H 2 ) 4 - C H ( N H 2 ) - C O O H
aromatic, such as phenylalanine, C H 2- C H ( N H 2) - C O O H
C H 2 · CH(NH 2 ) · COOH
heterocyclic, such as tryptophan,
H
sulfur-containing (aliphatic, neutral), such as methionine,
C H 3 · S C H 2 · C H 2 · CH(NH 2 ) · COOH.
Twenty-six amino acids are obtained from proteins by hydrolysis with
acids, alkalis, and enzymes. Altogether, about 170 amino acids have been
found so far in nature, either in the free form or linked to other compounds
(except proteins). Such amino acids have been detected in the circulatory
system of animals, as intermediates in metabolic processes or as components
of antibiotics, and in plants. Some of these acids have the unnatural D -
configuration.
Several of these are listed below.
γ-Methylene-glutamic acid, H O O C - C ( = C H 2 ) - C H 2 - C H ( N H 2 ) - C O O H
α-Aminoadipic acid, H O O C - C H 2 - C H 2 - C H 2 - C H ( N H 2 ) - C O O H
a-Amino-0-phenylbutyric acid, < ^ ^ > — C H ( C H 3 ) · CH(NH 2 ) · COOH
L-Homoserine, HO · C H 2 · C H 2 · CH(NH 2 ) · COOH

s-Methyl-L-cysteine, C H 3 · SCH 2 · CH(NH 2 ) · COOH
Butyrine, C H 3 · C H 2 · CH(NH 2 ) · COOH
II. Amino Acids 255
Some of these acids possess structural features uncommon in natural
products, e.g.,
H
and methylenecyclopropylglycine, C H 2 CH C H ( N H 2 ) COOH.
\ /
CH2
With only few exceptions, such as ß-alanine, N H 2 - C H 2 - C H 2 - C O O H

and γ-aminobutyric acid, N H 2 - C H 2 ( C H 2 ) 2 - C O O H , the natural amino acids
are α-amino acids.
Mixtures of amino acids may be separated by fractional distillation of
the esters and by selective precipitation of salts. However, the most useful
methods are column, paper, thin-layer, HPLC, and gas chromatography of
the free or esterified amino acids, as well as ionophoresis.
1. Synthesis of α-Amino Acids

a. Amination of a-halogenated acids
R C H 2- C O O H R C H B r - C O O H ^ > R C H N H 2 · COOH + N H 4 B r
The α-bromo acids are sometimes synthesized through the correspond-

ing malonic acid:
HOOC-CHR-COOH HOOC-CBrR-COOH RCHBr-COOH + C 0 2
Better methods are those using the esters of phthalimido-, benzamido-,

formamido-, or acetamido-malonic acid, the blocking groups being removed
by hydrolysis in the final step of the synthesis.
/COOC2H5
+ RX CONHCR
A l k y l halide
C O O C 2H 5
C O O C 2H 5
Diethylbenzamidomalonate
N H 2 CHR COOH +
b. Strecker synthesis
A cyanohydrin is treated with ammonia, and the resulting aminonitrile is then
hydrolyzed.
RCHO ^ RCH(OH)CN Ä RCH(NH 2 )CN R C H ( N H 2) C O O H
c. Reductive amination
Reduction of an α-keto acid in the presence of NH 3 to the desired amino acid
may be accomplished by chemical reducing agents or catalytically. The
mechanism of the reaction probably occurs via the imino acid.
RCOCOOH +NH3 R-C-COOH RCH(NH 2 )COOH + H 2 0

II
NH
d. Erlenmeyer azlactone synthesis
A c 20 / A c O N a NaOH
C 6H 5C H O + C H 2C O O H C 6H 5C H = C — C O
N H C O C 6H 5 Ν Ο
V
c
C f i H,
Na/Hg HCl
C6H5CH=CCOOH C 6H 5C H 2C H COOH
1 A
NHCOC.H
6 5 NHCOQH,
C 6H 5C H 2C H ( N H 2) C O O H + C 6H 5C O O H
2. Resolution Procedures
Various procedures for the resolution of synthetic racemic amino acids into
their active antipodes have been employed.
a. Biological procedures
Asymmetric oxidation or decarboxylation by microorganisms, such as Pénicil-
lium glaucum, whereby only one of the antipodes is converted into the
corresponding α-keto acid or amine, while the other remains and can be
isolated. More recently, enzymes have been employed for this purpose.
Lately, a good separation of amino acids has been obtained by gas-liquid
chromatography.
II. Amino Acids 257
b. Diastereoisomeric salts
This method is based on the formation of diastereoisomeric salts from the
racemic mixture and optically active bases (quinine, strychnine, brucine,
cinchonine, chloramphenicol).
( + ) B + ( d l ) A - * ( + ) Β · ( + )Α + ( + ) Β · ( - ) Α
The salts have different physical properties, e.g., different rotations.
The mixture of the salts formed is separated by a series of fractional crystal-
lizations, followed by Polarimetrie measurements.
Recently, thin-layer and gas-liquid chromatography have been used
successfully for the resolution and separation of racemic amino acids.
3. Biosynthesis of Amino Acids

It has long been known that there is a close interrelationship between the
metabolisms of carbohydrates and amino acids. The starting materials for the
biosynthesis of amino acids are certain products of carbohydrate metabolism,
e.g., pyruvic acid, oxaloacetic acid, and a-ketoglutaric acid. These com-
pounds can be converted, by transamination or reductive amination, to
alanine, aspartic acid, and glutamic acid. Glutamic and aspartic acids are in
turn the precursors of many amino acids. Thus, glutamic acid can be con-
verted into ornithine. Ornithine in turn is a precursor of citrulline and
arginine. Aspartic acid can give rise to ß-alanine, homoserine, and threonine.
The biosynthesis of tyrosine and phenylalanine by the shikimic acid pathway
has been established.
4. Peptides
Peptides are polyamides of amino acids and may be represented as follows:
Jn
A number of biologically active peptides are found in nature. Among the
simplest are the tripeptide glutathione, present in yeast, and folic acid,
present in liver, spinach, and yeast.
Examples of more complex peptides are gramicidin S, an antibiotic that
contains 22 amino acid residues in combination with two molecules of etha-
nolamine, and oxytocin—the major uterine-contracting and milk-ejecting
hormone of the posterior pituitary. Vasopressin, a naturally occurring
nonapeptide hormone, raises blood pressure by vasoconstriction. A number
of alkaloids containing peptides have been isolated from rye-ergot. Many

peptide antibiotics, such as penicillins, are now known.
HOOC C H ( N H 2 ) · C H 2 C H 2 CONH CH C O N H · C H 2 COOH

I
C H 2S H
Glutathione (y- glutamylcysteinglycine)
I ^ 3
CHCOOH
ο
Penicillin G
The first stage in the determination of the structure of a peptide is the

identification of its amino acid residues. This is done by hydrolysis and the use
of paper, thin-layer, HPLC, and vapor-phase chromatography, and electro-
phoresis. Another important method is the end-group analysis, which in-
volves the reaction of either the terminal amino or carboxyl groups.
The main objectives of peptide synthesis are to prepare the biologically
active natural peptides and to clarify the correlation between their structure
and biological activity.
The standard technique is based on building up long chains by repeated
condensations of individual amino acids. The following difficulties are en-
countered in such methods: the selection of suitable blocking groups that can
be effectively removed without disrupting the peptide bond; activation of the
carboxyl group for coupling without side reactions; selection of conditions
that will avoid racemization; isolation and purification of intermediate prod-
ducts before using them for the next step.
A new method of peptide synthesis was recently proposed by Merrifield.
In his solid-phase peptide synthesis, a peptide chain can be synthesized in a
stepwise manner from one end, while it is attached by a covalent bond at the
other end to an insoluble solid support. After the synthesis is complete, the
peptide chain can be cleaved from the solid phase to which it has been
anchored.
Merrifield's method was recently modified by Shemyakin and his co-
workers, who used a polymeric support in solution.
Katchalski and his coworkers have used insoluble polymeric reagents
for peptide synthesis, and have synthesized bradykinin and glutathione.
Katchalski's method calls for the addition of a solution of free peptide ester to
an insoluble, N-blocked active ester of an amino acid. Purification of in-
termediate peptides can be effected during the synthesis, since these peptides
are liberated in solution.
II. Amino Acids 259
In the Merrifield synthesis, peptide purification can be carried out only

after detachment of the final product from the polymeric carrier.
It is hoped that these accelerated techniques will make possible the
synthesis of large polypeptides and perhaps even of proteins.
B. Isolation of Glutamine from Red Beet

1. Introduction
The first indication of the possible existence of glutamine in nature was
reported by Scheibler (1) in 1868 during his investigation of the isolation of
asparagine and aspartic acid from beet sugar molasses. In 1883, Schulze and
Bosshard (2) isolated pure glutamine from an aqueous extract of beet roots.
The isolation of L-glutamine from gliadin was accomplished by Damodarm
(3). Glutamine can also be obtained from many other plant tissues, but beet
roots are the most readily available material and are also one of the richest
sources of this compound. Furthermore, most tissues additionally contain a
considerable amount of asparagine, which can be separated only by trouble-
some fractional crystallization. The quantity of asparagine in beet root is so
small that it does not raise any problems.
Glutamine is an anticonvulsant, but is applied only in cases refractory to
drug therapy.
H O O C · C H ( N H 2 ) · C H 2 ·CH 2 C O N H 2
Glutamine
2. Principle
In the following procedure ( 4 ) , the content of natural glutamine in the root
tissue of the common red beet (Beta vulgaris) is increased by treating the
plants with dilute ammonium sulfate solution. The roots are first frozen and
then thawed in order to reduce the permeability of the cells. They are then
ground and extracted with cold water, and the extract is treated with basic
lead acetate to precipitate interfering substances. After filtration, the gluta-
mine is precipitated with mercuric nitrate. The precipitate is decomposed
with hydrogen sulfide and filtered, and the solution is neutralized with am-
monium hydroxide and concentrated in vacuo at low temperatures. The
glutamine is crystallized in the presence of 6 0 % alcohol and purified by
recrystallization. The quantity of glutamine obtained depends on its content
in the original tissue.
It should be noted that mercuric nitrate is not a specific precipitant for
glutamine. Asparagine is also precipitated quantitatively, accompanied by
small amounts of other amino acids, e.g., arginine, lysine, tyrosine, and
cystine.
3. Apparatus
Blender Vacuum desiccator
Meat mincer Vacuum distillation assembly
4. Materials
Ammonium hydroxide Lead acetate (basic)
Ammonium sulfate Lead oxide (litharge)
Celite Mercuric oxide (red)
Ethanol Nitric acid
Ether Red beet
Hydrogen sulfide Sodium hydroxide
Lead acetate
5. Time
Soaking of beet roots: 24 hours
Laboratory procedure: 8 - 9 hours
6. Procedure
a. Extraction
One kg red beet roots is soaked for 1 day in 5 liters 0.2M ammonium sulfate
solution, and then washed thoroughly and kept in cold storage. The coarsely
sliced frozen roots are ground in a meat mincer. The cold pulp is warmed at
room temperature, and the juice is expressed with a hydraulic press or a
blender, or convenient quantities of the tissue may even be wrapped in strong
cotton cloth and the juice wrung out by hand. In both cases, a liberal volume
of wash water should be used. The total effluent (about 1.5 liters) is treated
with basic lead acetate reagent (prepared by dissolving 18 g lead acetate in
about 70 ml hot water to which 11 g lead oxide (litharge) is then added in
powdered form). The mixture is boiled with stirring for half an hour, cooled,
filtered, and diluted with water to 100 ml. Alternatively, an approximately
2 5 % solution of commercial basic lead acetate may be used in slight excess
(approximately 80 ml) and immediately filtered on a Büchner funnel fitted
with filter paper covered by a thin layer of Celite. The precipitate is packed
down hard and washed three times with water, a total of 600 to 800 ml being
used. The clear yellow filtrate is treated with mercuric nitrate reagent (pre-
pared by slowly adding 22 g high-grade red mercuric oxide to 16 ml concen-
trated nitric acid with stirring). Water (16 ml) is then added, and the mixture
is refluxed for 3 or 4 hr or until the oxide has completely dissolved. The
solution is cooled and treated with IN sodium hydroxide until a faint perma-
nent opalescence is noted; it is then diluted to 100 ml and filtered. It is kept in
a dark bottle.
II. Amino Acids 261
The suspension is then neutralized to approximately pH 6 by addition of

10% sodium hydroxide, accompanied by vigorous stirring. The operations up
to this point require about 6 hr. It is usually convenient to allow the precipi-
tate to settle overnight. The clear supernatant liquid is siphoned off. The
precipitate is transferred to a Büchner funnel fitted with a filter paper covered
with a thin layer of Celite, and is washed three times with a total of 500 ml
water. The precipitate is suspended in the minimal necessary amount of
water, all lumps being broken up, and transferred to a 1-liter filter flask. To
this suspension is added 0.25 ml 4N sulfuric acid. The flask is placed on a
shaking machine, and hydrogen sulfide is passed through for about 2 hr with
continuous agitation. Air is then passed through the suspension for a short time
to remove most of the excess hydrogen sulfide, and the precipitate is filtered
and, washed with 100 to 200 ml water. The clear, pale yellow filtrate is
transferred to a 1-liter flask and concentrated in vacuo for about 20 min, at a
bath temperature of 60°C, to remove the last traces of hydrogen sulfide. The
solution is then neutralized to approximately pH 6 by the careful addition of
3 to 5 ml 157V ammonium hydroxide. Equal portions of the solution are then
poured into two 500-ml flasks and concentrated in vacuo, at a bath tempera-
ture of 60 to 65°C, to a total volume of about 100 ml. The concentrated
solutions are combined, treated with a little Norit at 60°C, and filtered until
perfectly clear. Concentration is then continued in a 250-ml flask until a
sludge of crystals is obtained. Once the solution has become fairly concen-
trated, the temperature should be carefully controlled.
After the vacuum is released, the contents of the flask are warmed to 60
to 70°C, whereupon most of the crystals dissolve. Two volumes of warm
alcohol are then added, and the flask is chilled overnight. The crystals are
filtered, washed with cold 5 0 % ethanol and then with 9 5 % ethanol and ether,
and dried over sulfuric acid in a vacuum desiccator.
The quantity of glutamine obtained depends on its content in the orig-
inal tissue. Approximately 3.5 g crude material can be obtained from the
1 kg beet roots which was treated with ammonium sulfate.
b. IR spectrum of glutamine (in CCI4)

- 1
3403 c m : Ν—Η stretching (anhydrous glutamine)
1690: C = 0 stretching of — C O N H 2 (amide I band)
1639: COO~ asym. stretching
1586: N H 2 in-plane bending of the amide group
1487: asym. C H 2 bending
1428: sym. C O O " stretching
1411: C—Ν stretching
1361: sym. C H 2 bending
1336: C—H bending
c. NMR spectrum of glutamine
OOC—CH(NH 3 >—(CH 2 ) 2 —CONH 2

(b) (c) (a) (d)
Position δ (ppm)
a 2.74
b 4.53
c 7.80
d 8.26
References
1. Scheibler, C. (1868). Ber. 2, 296.
2. Schulze, Ε . , and Bosshard, E . (1883). Ber. 16, 312.
3. Damodarm, M. Biochem. J. 26, 235 (1932).
4. Vickery, Η. B . , and Pucher, G. W. (1949). Biochem. Prepns. 1, 44.
Recommended Review
1. Archibald, R . M. (1945). Chemical characteristics and physiological roles of glutamine.

Chem. Revs. 37, 161.
C. Preparation of D-Tyrosine from L-Tyrosine
1. Introduction
The resolution of tyrosine was first carried out by Fischer (1). Treatment of
jV-benzoyl-DL-tyrosine with brucine yielded an insoluble salt corresponding
to the L-isomer, while treatment with cinchonine yielded an insoluble salt
corresponding to the D-isomer. D-Tyrosine has also been obtained by the
action of brucine on formyl-DL-tyrosine ( 2 ) , and on iV-acetyl-DL-tyrosine (3).
COOH
H 2N— C - H
OH
Tyrosine
II. Amino Acids 263
2. Principle
In the following procedure ( 4 ) , the natural isomer, L-tyrosine, is racemized
with excess acetic anhydride. The diacetyl-DL-tyrosine produced is hydroly-
zed to N-acetyl-DL-tyrosine monohydrate.
Crystallization from ethanol of the brucine salts of the monohydrate
yields the salt of the D-isomer. Upon decomposition N-acetyl-D-tyrosine is
obtained. Hydrolysis of this compound gives D-tyrosine; overall yield, 6 5 % .
3. Apparatus
Reflux assembly
4. Materials
Acetic acid Chloroform Sodium hydroxide
Acetic anhydride Ethanol, absolute Sulfuric acid
Acetone Ethanol, 9 5 % L-Tyrosine
Brucine Hydrochloric acid
5. Time
4 overnight periods for crystallization
8 - 9 hours, laboratory procedure
6. Procedure
a. A/-Acetyl-DL-tyrosine monohydrate
L-Tyrosine (18 g) is suspended in 100 ml of water in a 500-ml beaker, to which
is added 100 ml 2 Ν sodium hydroxide exactly standardized against 6N sul-
furic acid. The solution is stirred continuously, and 66 ml redistilled acetic an-
hydride is added in ten 6.6-ml portions at 10-min intervals. The warm reaction
mixture is placed in a water bath (60 to 70°C) for 6 hr. It is then exactly
neutralized with 6N sulfuric acid, and the mixture is concentrated in vacuo.
To remove additional acetic acid, the distillation is continued after the sepa-
rate addition of two 20-ml portions of water. The thick syrup and sodium
sulfate are extracted with one 50-ml portion and four 10-ml portions of
acetone. The extracts are combined and evaporated to dryness in vacuo, and
the residue is dissolved in 20 ml water. The O-acetyl group is hydrolyzed
by the addition of 80 ml 2 Ν sodium hydroxide, the reaction being tested in
order to ensure that it is strongly alkaline to Phenolphthalein. After 30 min at
room temperature, the calculated amount of 6 TV sulfuric acid required to
exactly neutralize the alkali is added. The solution is concentrated, giving
crude N-acetyl-DL-tyrosine as a thick syrup. This is dissolved in 60 ml water,
and the solution is allowed to stand in the cold until crystallization occurs
(about 24 hr). Occasional stirring promotes more rapid crystallization and
gives a material that is more readily filtered. The yield of crystalline N-acetyl-
DL-tyrosine monohydrate is 21 g; mp 94-95°C.
b. Resolution of A/-acetyl-Di_-tyrosine
In a 250-ml Erlenmeyer flask are placed 12 g JV-acetyl-DL-tyrosine monohy-
drate, 19.7 g anhydrous brucine, and 160 ml absolute ethanol. The mixture is
heated to boiling to ensure complete solution. The flask is allowed to stand at
room temperature until crystals begin to separate, whereupon the solution is
stirred well, and the container is scratched to promote further crystallization.
The best yields are obtained if the stoppered container is stored in the cold,
with occasional stirring, for 2 or 3 days. During this time interval, a little more
than half of the total salt is obtained. The crystals are filtered off quickly,
pressed firmly, and washed with 5 ml cold absolute ethanol. The air-dried
material should at this stage weigh 16.5-17 g. The salt is purified by 3 or 4
recrystallizations from 9 5 % ethanol. The recrystallized, air-dried material,
mp 155°C, contains from 7 to 12% water of hydration. Because the com-
pletely anhydrous salt is hygroscopic, dehydration is achieved by drying
in vacuo at 100°C. The dried sample is weighed and dissolved in 25 ml 9 5 %
ethanol, and the optical activity is determined. A 0 . 5 % solution of the an-
hydrous salt gives [ a ] d - 42.3°. An average yield of 26 g pure anhydrous
salt is obtained.
c. Acetyl-D-tyrosine
A quantity of air-dried salt representing 12.3 g anhydrous compound is dis-
solved by warming in 20 volumes water. The solution is rapidly cooled to
approximately 40°C, and 20 ml 2 TV sodium hydroxide is added with thorough
stirring. After 12 hr in the cold, the brucine tetrahydrate is filtered off and
thoroughly washed with 5 portions of cold water. The combined alkaline
filtrates are extracted five times with chloroform to remove the last traces of
brucine. The calculated amount of 6 TV sulfuric acid is added, and the solution
is evaporated to dryness in vacuo. The residue is extracted with acetone, and
the acetone solution is evaporated to dryness. A small portion of the residue
is recrystallized from a little water, giving acetyl-D-tyrosine, mp 153-154°C,
[a]D - 48.3°.
d. D-tyrosine
The acetone-soluble residue of acetyl-D-tyrosine is dissolved in 44 ml 5 Ν
hydrochloric acid and hydrolyzed by gently refluxing the solution for 2.5 hr.
The excess acid is removed by evaporating to dryness, adding three portions
of water, and reevaporating to dryness. The residue is dissolved in 40 ml
water and treated with Norit. The solution is made slightly alkaline with
II. Amino Acids 265
sodium hydroxide and then just acid to litmus with a few drops of acetic acid.
After 24 hr in the cold, the precipitated tyrosine is filtered off and washed
with cold water until free of chloride ion, and then with 2 portions of 9 5 %
ethanol and 2 portions of ether. By this method, 3.2 g D-tyrosine is obtained
from 0.02 mole brucine salt.
References
1. Fischer, E . , (1900). Ber. 33, 3638.
2. Abderhalden, Ε . , and Sickel, H. (1923). Z. Physiol. Chem. 131, 277.
3. Sealock, R . R . (1946). / . Biol. Chem. 166, 1.
4. Sealock, R . R . (1949). Biochem. Prepns. 1, 7 1 .
Recommended Review
1. Greenstein, J . P. (1954). The resolution of racemic α-amino acids. In "Advances in Protein
Chemistry." (M. L. Anson, K. Bailey, and J . T . Edsall, eds.), Vol. 9, p. 121. Academic
Press, New Y o r k .
D. Synthesis of DL-/?-Phenylalanine
1. Introduction
DL-Phenylalanine was first prepared in 1882 by Erlenmeyer and Lipp (1) by
the action of ammonia and hydrogen cyanide on phenylacetaldehyde. The
classical synthesis of phenylalanine by the condensation of benzaldehyde with
hippuric acid in the presence of sodium acetate-acetic anhydride was first
described by Plochl ( 2 ) , and later by Erlenmeyer (3), who established the
constitution of the intermediate azlactone. This procedure was later improved
by Harington and McCartney (4). The method described below was intro-
duced by Gillespie and Snyder (5) and is a simplification of the procedure of
Harington and McCartney. A similar method was recently elaborated by
Herbst and Shemin (6). In 1911, Wheeler and Hoffman (7) reported a
synthesis of phenylalanine that involves the condensation of benzaldehyde
and hydantoin. Phenylpyruvic acid, after conversion to its oximino derivative
of phenylhydrazone, may be reduced to yield /3-phenylalanine (8). Aminoma-
lonic esters have been used as precursors in the synthesis of phenylalanine
(9). Albertson and Tullar (10) used substituted cyanoacetic esters. In several
syntheses the α-bromo intermediate is aminated at some stage of the reaction
sequence ( 1 1 , 1 2 ) . A method involving the Curtius rearrangement was de-
veloped by Gagnon, Gaudry, and King (13). An interesting synthesis of
phenylalanine from cinnamic acid was recently reported by Yukawa and
Kimura (14).
/3-Phenylalanine is an essential amino acid. The recommended daily
uptake for a normal adult male is 2.2 g.
H Η Η O
ι /-ι II Η,Ο
H-CH-COOH C-C-C-OH
I I
NHOC C 6 H 5 HO N H O C C 6 H 5
Benzaldehyde
Hippuric acid
Ο Ο
II
/ VcH=C-C-0-H CH=C-C
I Ο
HN-C-QH,
II
Ο Η ΟΗ
/ \ ° 2 H 2Q
Τ + Η Γ C H 2C H ( N H 2) - C O O H +
N=C DL-/?-Phenylalanine
X
C6H5
^zlactone of α-benzoyl cinnamic acid
<^ y-COOH
Benzoic acid
2. Principle
In the following method (5), benzaldehyde is condensed with hippuric acid to
form an azlactone. The latter, on reduction and hydrolysis, by means of red
phosphorus-hydriodic acid, gives DL-jß-phenylalanine and benzoic acid. Since
the isoelectric pH of phenylalanine is 5.9, it is precipitated from the solution
by neutralization to Congo red with dilute ammonia.
3. Apparatus
Electric hot plate
Stirring assembly
4. Materials
Acetic acid, glacial Ethanol, 9 5 % Phosphorus, red
Acetic anhydride Ether Sodium acetate
Ammonium hydroxide Hippuric acid Sodium sulfite
Benzaldehyde Hydriodic acid
II. Amino Acids 267
5. Time
7 - 8 hours
6. Procedure
a. Azlactone of a-benzoylaminocinnamic acid

A mixture of 26.5 g benzaldehyde, 45 g powdered dry hippuric acid, 20.5 g
freshly fused sodium acetate, and 150 g (140 ml) high-grade acetic anhydride
in a 500-ml Erlenmeyer flask is heated on an electric hot plate, with constant
shaking. The mixture becomes almost solid and then, as the temperature
rises, gradually liquefies and turns deep yellow in color. As soon as the
contents have liquefied completely the flask is transferred to a steam bath and
heated for 1 hr. During this period, a part of the product separates as deep
yellow crystals. When heating is completed, 200 ml alcohol is added slowly to
the contents of the flask. During this addition, the flask is cooled slightly to
lessen the vigor of the reaction. The reaction mixture is then cooled, and the
yellow crystalline product is fltered with suction and washed on the filter with
two 25-ml portions of ice-cold alcohol, and finally with two 25-ml portions of
boiling water. After drying, the almost pure product weighs 3 9 - 4 0 g ( 6 2 - 6 4 %
yield); mp 165-166°C. This material is sufficiently pure for use in the prepara-
tion of phenylalanine. By crystallization from 150 ml benzene a product
melting at 167 to 168°C is obtained.
b. DL-jß-Phenylalanine
In a 1-liter three-necked, round-bottomed flask fitted with a reflux condenser,
a mechanical stirrer, and a dropping funnel, are placed 25 g azlactone of
α-benzoyl-aminocinnamic acid, 20 g red phosphorus, and 135 g (125 ml) ace-
tic anhydride. Over a period of about 1 hr 195 g (125 ml) 5 0 % hydriodic
acid are added with stirring. During this addition the reaction mixture may
solidify. If this occurs, the stirrer is stopped, and about 5 ml hydriodic acid
solution is stirred into the cake with a glass rod. The mass then becomes suf-
ficiently fluid to permit use of the mechanical stirrer. The mixture is re-
fluxed for 3 to 4 hr and, after cooling, is filtered with suction. The unreacted
phosphorus is washed on the filter with two 5-ml portions of glacial acetic
acid, and discarded. The filtrate and washings are evaporated to dryness,
under reduced pressure, in a 500-ml Claisen flask heated in a water bath.
100 ml is added to the residue in the Claisen flask, and evaporation to dryness
is repeated. To the residue in the flask are added 150 ml water and 150 ml
ether, and the mixture is shaken until solution is complete. The aqueous layer
is separated and extracted three times with 100-ml portions of ether. The
ether extracts are discarded. The aqueous solution is heated on a steam bath
with 2 to 3 g Norit and a trace of sodium sulfite until all dissolved ether has
been removed. The solution is filtered, and the filtrate is heated to boiling and
neutralized to Congo red with 1 5 % ammonia. About 25 ml ammonia is

usually required. The phenylalanine separates as colorless plates which,
when cold, are filtered off and washed thoroughly on the filter with two 30-ml
portions of cold water.
The yield is 10.5-11 g ( 6 3 - 6 7 % ) of a product that decomposes at 284 to
288° C.
c. Phenylalanine
C—C—COOH
ι :
Hb NH2
1
c. H NMR
a = 3.11 1H interchange.
b = 3.31 1H.
c = 4.01 1H
d = 7.40 5H
e. Mass Spectrum
C 9 H n N 0 2 , Mol. wt. 165.
m/z 165(7.43%) 92(18%) 74(100%)
120(74%) 91(55%) 65(10%)
103(9%) 77(7%) 28(15%)
f. IR Spectrum of Di_-ß-phenylalanine (in nujol)

1
303, 2898, 2710, 2154 c m " : N H 3
1623: N H 3 asym. bending
-
1589: C O O asym. bending
1503: N H 3 sym. bending
1401: C O O " sym. bending
1310: CH bending
1212: N H 3 rocking
1150: C—CN asym. stretching.
References
1. Erlenmeyer, E . , and Lipp, A . (1882). Ber. 15, 1006.
2. Plochl, J . (1883). Ber 16, 2815.
3. Erlenmeyer, E . (1893). Ann. 275, 1.
4. Harington, C. R . , and McCartney, W. (1927). Biochem. J. 2 1 , 852.
5. Gillespie, H. B . , and Snyder, H. R . (1943). Org. Synth. Coll. 2, 489.
II. Amino Acids 269
6. Herbst, R . M . , and Shemin, D . (1943). Org. Synth. Coll. 2, 421.

7. Wheeler, H. L . , and Hoffman, C. (1911). Am. Chem. J. 4 5 , 368.
8. Granacher, C. (1922). Helv. Chim. Acta 5 , 610.
9. Galat, A . (1947). J. Am. Chem. Soc. 6 9 , 965.
10. Albertson, N. F . , and Tullar, B . F . (1945). J. Am. Chem. Soc. 67, 502.
11. Marvell, C. S. (1955). Org. Synth. Coll. 3, 705.
12. Gaudry, R . (1945). Can. J. Research 2 3 B , 234.
13. Gagnon, P. E . , Gaudry, R . , and King, F . E . (1944). / . Chem. Soc. 13.
14. Yukawa, Y . , and Kimura, S. (1957). J. Chem. Soc. Japan 78, 454.
Recommended Review
1. Dunn, M . S . , and Rockland, L . Β . (1947). The preparation and criteria of purity of the amino
acids. In "Advances in Protein Chemistry", M. L . Anson, and J . T . Edsall, (eds.), Vol. 3,
E. Preparation of Glycylglycine by Mixed Carboxylic-Carbonic

Acid Anhydride Method
1. Introduction
Treatment of a solution of an acylamino acid or acylated peptide with one
equivalent each of an alkyl chlorocarbonate and a tertiary amine, e.g.,
triethylamine, under anhydrous conditions gives rise to the formation of the
mixed carboxylic-carbonic acid anhydride. Condensation of the anhydride
in situ with the alkali-metal salt of the amino acid or peptide leads to the
formation of the desired peptide derivative, in addition to an alcohol and
carbon dioxide. Conversion of this product to the corresponding free acid
makes possible further condensation with another equivalent of amino acid
by similar condensation. This method calls for adequate protection of reactive
groups; this is given by the carbobenzoxy (Cbzo) group, which was intro-
duced into peptide chemistry by Bergmann and Zervas in 1932 (1). This
group is to this day the most widely used amino-protective group. Car-
bohenzoxy amino acids are easily prepared without racemization and are
converted without difficulty into peptides by the mixed anhydride, dicyclo-
hexylcarbodiimide, and p-nitrophenyl ester methods. In addition to its pro-
tective effect against racemization of the amino acid, this group possesses a
further advantage in that it can be removed by a great variety of methods:
catalytic hydrogénation at NTP; hydrobromic acid (gas) in glacial acetic acid
(2) (the hydrobromide of the free peptide usually precipitates upon addition
of ether, which also dissolves the benzyl bromide formed during the reac-
tion); sodium in liquid ammonia. The reductive action of sodium in liquid
ammonia removes not only the carbobenzoxy group but also 5-benzyl, N-
(imino)-benzyl, and other groups. It is preferentially employed at the end of a
synthesis for the simultaneous removal of several of these groups.
1. C 6H 5C H 2O H + COCl2 • C 6 H 5 C H 2 O C O C l + HCl
Benzyl alcohol Phosgene Benzyl chloroformate
2. C 6H 5C H 2O C O C l + H 2N C H 2C O O H
Glycine
C 6 H 5 C H 2 O C O N H C H 2 C O O H + NaCl
Carbobenzoxyglycine
a. C 2H 5O C O C l
3. C 6H 5C H 2O C O N H C H 2C O O H
° b. N H 2C H 2C O O N a
c. HCl
C 6H 5C H 2O C O N H C H 2C O N H C H 2C O O H + C 0 2 + C 2H 5O H
Carbobenzoxyglycylglycine
a
4. C 6H 5C H 2O C O N H C H 2C O N H C H 2C O O H HBr/CH 3coon >
b. pyridine
N H 2C H 2C O N H C H 2C O O H + C 6H 5C H 2B r + C 0 2
Glycylglycine Benzyl bromide
2. Principle
Benzyl chloroformate is prepared by bubbling phosgene through cold benzyl
alcohol (3). Treatment of glycine with benzyl chloroformate in alkaline solu-
tion forms carbobenzoxyglycine, which is transformed by ethyl chloroformate
(in the presence of triethylamine) to acid chloride. This chloride in turn
condenses with sodium glycinate to yield sodium carbobenzoxyglycyl glycin-
ate, this stage being accompanied by carbon dioxide evolution. Acidification
of the product yields carbobenzoxyglycylglycine. Addition of gaseous hy-
drogen bromide in glacial acetic acid causes smooth nonhydrolytic cleavage
of the carbobenzoxy group, yielding glycylglycine hydrobromide. The free
peptide is obtained by adding excess of pyridine.
3. Apparatus
Three-necked flask with stirrer and dropping funnels
4. Materials
Acetic acid, glacial Ethanol, absolute Phosgene
Acetone Ethyl chloroformate Pyridine
Benzyl alcohol Hydrobromic acid Sodium hydroxide
Calcium chloride Hydrochloric acid Toluene
Chloroform Methanol Triethylamine
II. Amino Acids 271
5. Time
1 0 - 1 2 hours
6. Procedure
a. Benzyl chloroformate
A 500-ml round-bottomed flask is fitted with a rubber stopper carrying an
outlet tube and a delivery tube extending to the bottom of the flask. In the
flask is placed 50 g dry toluene, and the apparatus is weighed. The flask is
then cooled in an ice bath, and phosgene is bubbled into the toluene until
10.9 g has been absorbed (about 1 hr is required for this step). The outlet
gases are passed through a flask containing toluene in order to remove any
phosgene, and then through a calcium chloride tube to a gas trap. After the
absorption of phosgene is completed, the connection to the phosgene tank is
replaced by a separatory funnel. The reaction flask is gently shaken while
10.8 g (10.4 ml) redistilled benzyl alcohol is added rapidly via the separatory
funnel. The flask is allowed to stand in the ice bath for half an hour and at
room temperature for 2 hr.
The solution is then concentrated under reduced pressure, at a tempera-
ture not exceeding 60°C, in order to remove hydrogen chloride, excess
phosgene, and the major portion of the toluene. (In order to prevent the
escape of phosgene, a toluene trap is inserted between the apparatus and the
water pump).
The residue weighs 2 0 - 2 2 g and contains 1 5 - 1 6 g benzyl chloroformate.
The amount of benzyl chloroformate present in this solution may be esti-
mated by preparing the amide from a small aliquot portion, or it may be
safely calculated by assuming a minimum yield of 9 0 % of the theoretical
amount based on the benzyl alcohol used. Note: All operations must be
performed in a well-ventilated hood!
b. Carbobenzoxyglycine
A solution of 7.5 g glycine in 25 ml 4 Ν sodium hydroxide is placed in a
200-ml three-necked flask fitted with a mechanical stirrer and two dropping
funnels. The flask is cooled in an ice bath, and 17 g benzyl chloroformate and
25 ml 4 Ν sodium hydroxide are added simultaneously to the vigorously
stirred solution over a period of 20 to 25 min. The mixture is stirred for an
additional 10 min. The toluene layer is separated, and the aqueous layer is
extracted once with ether.
The aqueous solution is cooled in an ice bath and acidified to Congo
red with concentrated hydrochloric acid. The precipitate is filtered off, washed
with small portions of cold water, and dried in air. It consists of almost pure
carbobenzoxy-glycine and weighs 1 8 - 1 9 g ( 8 6 - 9 1 % ) ; mp 119-120°C. The
material may be recrystallized from chloroform; mp 120°C.
c. Carbobenzoxyglycylglycine
A solution of 16.8 g carbobenzoxyglycine in 200 ml dry toluene is placed in a
500-ml three-necked flask fitted with a mechanical stirrer and a dropping
funnel equipped with a calcium chloride tube. 8.15 g triethylamine is added to
the stirred solution, whereupon the acid dissolves, leaving the salt in solution.
The flask is cooled in an ice-salt bath and 8.6 g ethyl chloroformate is added
to the vigorously stirred solution over a period of 15 min. The mixture is
stirred for an additional 45 min, and a solution of 6 g glycine in 80 ml 1 TV
sodium hydroxide is added. The mixture is stirred vigorously for 2 to 3 hr,
during which time it is permitted to warm to room temperature. Carbon
dioxide is evolved during this interval. The toluene layer is now separated and
extracted with a 5 % sodium hydroxide solution. The aqueous solutions are
combined and extracted three times with 50-ml portions of ether.The aqueous
solution is then heated on a water bath at 50°C and the dissolved ether is
removed under reduced pressure. The solution is then cooled in an ice bath
and acidified to Congo red with concentrated hydrochloric acid. After about
45 min, the product precipitates and is filtered on a Büchner funnel and
washed with small portions of cold water. It is dried in air and recrystallized
from methanol. The product melts at 178°C; yield 7 0 - 8 0 % .
d. Glycylglycine
Eight g carbobenzoxyglycylglycine is suspended in 25 ml glacial acetic acid in
a 250-ml round-bottomed flask fitted with a gas inlet tube and a calcium
chloride drying tube. The flask is placed in an oil bath heated to 60°C, and a
stream of dry hydrogen bromide is bubbled into the solution for 1 hr. Carbon
dioxide is evolved during the bubbling. Upon cessation of gas evolution,
150 ml dry ether is added to precipitate the glycylglycine hydrobromide. The
flask is left in an ice bath for 1 hr, its contents are filtered, and the residue is
washed with several portions of anhydrous ether.
The free peptide is obtained by dissolving the salt in a little water,
adding excess pyridine, and precipitating with absolute ethanol. The precipi-
tate is then filtered, washed with ether and acetone, and dried in air.
e. IR spectrum of glycylglycine (in nujol)

- 1
3300 c m : Ν—H stretching (of—CONH—)
3080: bonded Ν—H
2920: asym. C—H stretching of C H 2
2840: sym. C—H stretching of C H 2
1680: C = 0 stretching of non-ionized carboxyl
1655: C = 0 stretching of—CONH— (amide I band)
1608: C—Ο asym. stretching of C O O "
1550: mainly Ν—Η deformation mixed with C—Ν stretching (amide II
band)
II. Amino Acids 273
1460: C H 2 deformation
1395: ionized carboxyl group from zwitterion form
1330, 1275: mainly C—Ν stretching mixed with Ν—Η bending (amide
III band)
1015: skeletal vibration
f. NMR spectrum of glycylglycine
H 3N C H 2C O N H C H 2C O O ~
(b) (a) (c)
Position δ (ppm)
a 4.29
b 7.54
c 7.95 (doublet)
References
1. Bergmann, M . , and Zervas, L. (1932). Ber. 6 5 , 1192.
2. Ben-Ishay, D . (1954). J. Org. Chem. 19, 62.
3. Carter, H. E . , Frank, R . L . , and Johnston, H. W. (1955). Org. Synth. Coll. 3, 167.
Recommended Reviews
1. Albertson, N. F . (1962). Synthesis of peptides with mixed anhydrides. In "Organic Reac-
tions" Vol. 12, p. 157. John Wiley, New York.
2. Boissonnas, R . A . (1965). Selectively removable amino-protective groups used in the synthesis
of peptides. In "Advances in Organic Chemistry" Vol. 3, p. 159. Interscience, New Y o r k .
F. Thin-Layer Chromatographic Enantiomeric Resolution of

Racemic Amino Acids
1. Introduction
Natural and synthetic chiral compounds (stereoisomers) show different bio-
logical and pharmacological activities. Usually the optical rotation is used as
an indication of the enantiomeric purity. However, estimation of the enan-
tiomeric (ee value) from optical rotation is not possible in cases where the a D
value of the pure enantiomer is unknown. Furthermore, a calculation of the
ee value may give erroneous results in the presence of impurities.
Gas chromatographic ( 1 , 2 ) and high-performance liquid chromato-
graphic ( 3 - 5 ) separations of enantiomers have been extensively studied.
These methods, however, are time consuming and require costly equipment,
and sometimes sample derivatization is necessary.
Chiral amino acids are required for the synthesis of biologically active
peptides, in asymmetric syntheses, and as pharmacological ingredients. The
enantiomeric separation of racemic DL-amino acids can be performed ef-
ficiently and quickly on Chiral plates (Macherey-Nagel).
2. Principle
The following procedure (6) is based on using Chiral thin-layer plates for the
separation of racemic amino acids, both natural and synthetic. The respective
enantiomers can be determined at trace levels.
3. Apparatus
T L C developing chambers
4. Materials
Acetonitrile Ninhydrin ( 1 % ) spray
Chiral T L C plates Phenylalanine
(such as Macherey-Nagel) Proline
Glutamine Tryptophan
Isoleucine Tyrosine
Methanol Valine
5. Time
Less than 2 hours
6. Procedure
The Chiral plates (10 x 20 cm; 0.25 thick) should be activated for 15 min at
100°C before use. Sample volume: 2 μΐ of the racemic mixture as a 1%
solution of amino acid (in methanol or methanol-water). Developing solvent
is methanol-water-acetonitrile ( 1 : 1 : 4 ) with chamber saturation. The de-
veloping time is 25 min. for 13 cm. Detection is accomplished by using 0 . 1 %
ninhydrin spray reagent followed by heating in an oven at 100°C.
The following racemic amino acids may be used: glutamine, isoleucine,
phenylalanine, proline, tryptophan, tyrosine, valine.
References
1. Frank, H., Woiwoode, W., Nicholson, G . , and Bayer, E . (1981). Liebigs Ann. Chem. 354.
2. Konig, W. Α . , Steinbach, Ε . , and Ernst, Κ. (1984). Angew Chem. 96, 516.
3. Lam, S., and Karmen, A . J . (1984). Chromatogr. 289, 339.
4. Roumeliotis, P., Unger, Κ. K . , Kurganov, Α . Α . , and Davankov, V . A . (1983). / . Chro-
matogr. 255, 51.
5. Alienmark, S. (1984). / . Biochem. Biophys. Methods 9, 1.
6. Gunther, Κ . , and Schickedanz, M. (1985). Naturwissen 72, 149.
II. Amino Acids 275
Recommended References
1. Stevenson, D . , and Wilson, I. D . , eds. (1987). "Chiral Separation." Plenum Press, New
York.
2. Poole, C. F . , and Poole, S. K. (1989). Modern thin-layer chromatography. Anal. Chem. 6 1 ,
1257A.
3. Jost, W . , and Houck, H. E . (1987). The use of modified silica gels in T L C and H P L C . Adv.
Chromatogr. 27, 129.
G. Reverse-Phase High-Performance Liquid Chromatography of

Amino Acids
1. Introduction
The separation of amino acids by liquid chromatography has been pursued by
many investigators in various fields of science, mainly in the area of amino
acids and protein chemistry ( 1 - 4 ) . The analysis of amino acids presents the
chromatographer with a challenging task owing to two main difficulties:
(1) Most of the amino acids are not amenable to easy detection with conven-
tional detectors. Thus frequently they undergo some sort of either pre- or
postcolumn derivatization procedure; (2) As a group, the amino acids cover a
very wide range of polarities, making isocratic analysis very difficult.
2. Principle
In the following procedure (5), the charge transfer complexes of copper of the
amino acids are analyzed by reverse-phase HPLC. Thus the mobile phase is
made up of a sodium acetate buffer (pH 5.6) containing cupric ions and
alkylsulfonate ion-pair reagent. The complexes absorb U V radiation with a
maximum around 235 nm and a molar absorptivity of about 6000 (for the 1:1
complex).
a. Instrumentation
The column is a Merck Lichrosorb R P i 8 cartridge, packed with 7 μ,ιη parti-
cles. The cartridge dimensions are 250 x 4 mm. A precolumn is connected
between the pump and the injector. It is refilled once a month with a mixture
of Partisil 10 silica gel and Partisil 10 ODS-3.
b. Solutes
To demonstrate the influence of each of the chromatographic variables, the
following amino acids are used as sample solutes: aspartic acid, glycine,
histidine, lysine, arginine, valine, methionine, threonine, hydroxyproline,
asparagine, and tyrosine. These amino acids cover a wide range of polarities
and hydrophobicities, and they represent all types of side chains. The amount
of injected amino acids is 2.4 nmol for all but the most retained solutes, for
which 10 nmol are introduced to the column.
c. Choice of buffer
It has been found that the complexation of Cu(II) by amino acids, and
consequently chromatographic retention, is more favorable at high pH.
However, at pH greater than 6, cupric hydroxide will precipitate out unless
some chelating agent, which is capable of strongly complexing copper ions, is
present in the mobile phase. On the other hand, the complexation should not
be too strong, for then amino acids chelation would greatly diminish, and the
benefits of cupric ions would be lost. In order to overcome these problems, an
acetate buffer at pH 5.6 is used.
d. Problems associated with use of Cu(ll) ions

Besides the buffer issue, several other chemical and technical difficulties are
attributed to the presence of cupric ions. Exposed metal parts of the system,
such as tubings, pump pistons, etc., can be subjected to chemical attack by
the copper ions in the mobile phase. The extent of corrosion is a function of
the mobile phase pH. The corrosion problem can be greatly minimized by the
following action: the mobile phase flow should not be stopped for long
periods. The system, including the column, should be rinsed thoroughly with
water and methanol whenever it will not be used for a while, e.g., overnight.
At least once a week, the system should be washed with 0.01 M E D T A in a
0.1 M acetate buffer. This treatment extends the lifetime of the column to
equal those of conventional reverse-phase systems.
e. Effects of alkylsulfonates
The copper complex of the amino acids, which is assumed to be in a 1:1 ratio
4
in the range of the Cu(II) concentration of 5 x 1 0 ~ M is probably positively
charged. Thus introducing an anionic species such as an alkylsulfonate should
enhance the retention via an ion-pair mechanism. It was found that when
hexane-, heptane-, or octanesulfonates were added to the copper-containing
mobile phases, the retention times of the test amino acids were verified
substantially. For the separation of all amino acids mentioned above, the
4
Cu(II) concentration was 5 χ 1 0 " M, and the buffer acetate concentration
was 0.1 M. The concentration of the sulfonates varied from zero to 0.005 M
or to 0.01 M. It was found that the extent of retention increase is a function
not only of alkylsulfonate concentration but also of the alkyl length.
3. Apparatus
High pressure liquid Chromatograph
4. Materials
Acetate buffer Asparagine
Arginine Heptanesulfonate
II. Amino Acids 277
Histidine Partisil 10 ODS-3

Hydroxyproline Partisil 10 silica gel
Lichrosorb R P 1 8 cartridge Threonine
Lysine Tyrosine
Methionine Valine
5. Time
45 minutes
6. Procedure
The mobile phase: 0.01 M acetate buffer (pH 5.6).
4
4 x 1 0 " M CuAc 2
4
8 x 1 0 " M Heptanesulfonate
Column: R P 1 8 , 250 χ 4 mm
Flow rate: 2 ml/min
Temperature: 45°C
The elution order of the amino acids is aspartic acid, glutamine, glycine,
serine, aspartic acid, hydroxyproline, threonine, histidine, proline, valine,
methionine, tyrosine, leucine, arginine. Thus the acidic amino acids elute
fast, while basic amino acids remain in the column for a longer period.
References
1. Grushka, E . , Levin, S., and Gilon, C. (1982). J. Chromatogr. 235, 401.
2. Gimpel, M., and Unger, K. (1983). Chromatographia 17, 200.
3. Chinnick, C. C. T. (1981). Analyst {London) 106, 1203.
4. Foucault, Α . , and Rosset, R . (1984). J. Chromatogr. 317, 4 1 .
5. Levin, S., and Grushka, E . (1985). Anal. Chem. 57, 830.
Recommended Reviews
1. Williams, A . P. (1982). H P L C in Food Analysis. In "Food Science and Technology."
( R . Macrae, ed.), p. 285. Academic Press, New York.
2. Pfeifer, R . F . , and Hill, D . W. (1983). "Advances in Chromatography." ( J . C. Giddings,
E . Grushka, E . Cazes, and P. R . Brown, eds.), Vol. 22, p. 37. Marcel Dekker, New York.
H. Gas-Liquid Chromatography of Amino Acids

I. Introduction
Free amino acids possess a zwitterionic structure, so they are not volatile and
must be transformed into a suitable volatile derivative before the chroma-
tography. Many attempts at employing gas-liquid chromatography for amino
acids have been recorded. The first technique was the oxidation of α-amino
acids with ninhydrin to the corresponding aldehydes, which were subjected
to G L C (1). Zlatkis, Oro, and Kimball (2) extended this approach to four
additional aliphatic amino acids. Bier and Teitelbaum (3) explored the utility
of several amines obtained from amino acids by decarboxylation. Bayer,
Reuther, and Born (4) separated the methyl esters of several amino acids.
More promising results have been obtained with derivatives in which both
amino and carboxyl groups have been masked. Youngs (5) chromatographed
the iV-acetyl-n-butyl esters of some amino acids and developed a quantitative
gas-liquid chromatographic method for their determination. Johnson, Scott,
and Meister (6) concluded that 7V-acetyl-ft-amyl esters give better results than
other esters. Saroff and Karmen (7) have used N-trifluoracetyl methyl esters,
and these derivatives were also utilized by Cruickshank and Sheehan (8).
Zomzely, Marco, and Emery (9) prepared /i-butyl-N-trifluoroacetyl deriva-
tives. Landowne and Lipsky (10) have used 2,4-dinitrophenyl derivatives, and
Ruhlmann and Giesecke (11) TV-trimethylsilyl esters. It is noteworthy that
Pollock and his coworkers (12) recently succeeded in resolving 21 racemic
amino acids by gas chromatography.
2. Principle
In the following method ( 6 ) , the amino acids are converted into iV-acetyl-n-
amyl esters by treatment first with amyl alcohol and anhydrous hydrobromic
acid, and then with acetic anhydride. The derivatives are detected by gas
chromatography on columns containing a very small percentage of the liquid
phase ( 1 % ) and at relatively low temperature: 125-150°C.
3. Apparatus
Gas Chromatograph
U-shaped glass columns
4. Materials
Acetic anhydride
Amino acids (see the table)
ft-Amyl alcohol
Benzene
Chromosorb W (60-80 mesh)
Hydrobromic acid (gas)
Polyethylene glycol (Carbowax 1540 or 6000)
5. Time
Conditioning of column: 24 hours
Analysis: 3 - 4 hours
II. Amino Acids 279
6. Procedure
a. Preparation of samples
1-10 mg amino acid is suspended in 20 ml amyl alcohol, and the mixture is
saturated with anhydrous hydrobromic acid. This procedure takes 2 - 4 min.
The flask containing the mixture is placed in an oil bath at 165°C, and
approximately one half the alcohol is removed by distillation at atmospheric
pressure. The remaining alcohol is evaporated in vacuo at 60°C. The residual
oil or crystalline material consisting of the amino acid ester hydrobromide is
mixed with 8 ml acetic anhydride and allowed to stand at 26°C for 5 min. The
solution is then evaporated in vacuo at 60° to a syrup, which is taken up in
n-amyl alcohol or benzene and used directly for chromatography. The prepa-
ration of samples by this procedure takes approximately 1 hr.
b. Preparation of columns
U-shaped glass columns, 2 - 8 feet in length and \ inch inner diameter, are
packed with polyethylene glycol coated on a solid support consisting of
acid-washed Chromosorb W. The support is prepared by adding a weighed
amount of the solid support to a solution of Carbowax in benzene. The
mixture is then stirred vigorously at its boiling point until most of the solvent
has evaporated. After removal of benzene in vacuo, the column is packed
and heated for 24 hr at 150°C, with a flow rate of argon of 150 ml/min.
Retention Times of Amino Acids
Amino Acid Retention Time (min)
a-Alanine 14
Valine 16
a-Aminobutyric acid 17
Isoleucine 19
Norvaline 20
Leucine 22
Norleucine 23
Glycine 24
β- Alanine 26
/3-Aminobutyric acid 28
Proline 29
y-Aminobutyric acid 32
Ornithine 33
Threonine 35
Serine 39
Phenylalanine 60
Aspartic acid 84
Glutamic acid 102
Tyrosine 132
The columns are maintained at 125 to 155°C. The flash heaters are set at
300°C, and the temperature of the detectors is maintained at 225°C. The flow
rate of the carrier gas is adjusted to constant values between 60 and
240 ml/min as measured at the outlet. The samples are introduced into the
column in n-amyl alcohol or in a benzene solution.
Derivatives of alanine, valine, isoleucine, the leucine emerge from the
8-ft column packed with Chromosorb W coated with 1% Carbowax 1540 at
125°C. Flow rate 60 ml/min. Following the appearance of leucine, the column
temperature is sharply increased to 148°C, and the other amino acids emerge
at this temperature. The retention times of amino acids are presented in the
previous table.
References
1. Hunter, I. R . , Dimick, K. P., and Corse, J . W. (1956). Chem. Ind. (London), 294.
2. Zlatkis, Α . , Oro, J . F . , and Kimball, A. P. (1960). Anal. Chem. 32, 162.
3. Bier, M., and Teitelbaum, C. (1959). Ann. Ν. Y. Acad. Sei. 72, 641.
4. Bayer, E . , Reuther, Κ. Η., and Born, F . (1957). Angew. Chem. 69, 640.
5. Youngs, C. G. (1959). Anal. Chem. 3 1 , 1019.
6. Johnson, D . E . , Scott, S. J . , and Meister, A . (1961). Anal. Chem. 33, 669.
7. Saroff, Η. Α . , Karmen, Α . , and Healy, J . W. (1960). Anal. Biochem. 1, 344.
8. Cruickshank, P. Α . , and Sheehan, J . C. (1964). Anal. Chem. 36, 1191.
9. Zomzely, C , Marco, G . , and Emery, E . (1962). Anal. Chem. 34, 1414.
10. Landowne, R . Α . , and Lipsky, S. R . (1963). Federation Proceedings 22, 235.
11. Ruhlmann, K . , and Giesecke, W. (1961). Angew. Chem. 73, 113.
12. Pollock, G . E . , and Oyama, V . I. (1966). J. Gas Chromatogr. 126.
Recommended Reviews
1. Karmen, Α . , and Saroff, H. A . (1964). Gas-liquid chromatography of the amino acids. In
"New Biochemical Separations," ( A . T. James, and L. J . Morris, ed.), p. 81. Van Nostrand,
London.
2. Weinstein, Β . (1966). Separation and determination of amino acids and peptides by gas-liquid
chromatography. In "Methods of Biochemical Analysis," ( D . Glick, ed.), Vol. 14, p. 203.
Interscience, New York.
3. Blackburn, S. (1983). " C R C Handbook of Chromatography of Amino Acids and Amines,"
Vol. 1. C R C Press, New York.
I. Test Tube and Glass Rod Thin-Layer Chromatography of

Amino Acids
1. Introduction
Several investigators ( 1 - 5 ) have recently described the rapid preparation of
microchromatoplates from microscope slides and from test tubes coated on
their inner surface ( 6 - 7 ) .
II. Amino Acids 281
2. Principle
In the following method ( 8 ) , test tubes coated with silica gel G on their outer
surface and glass rods are utilized for thin-layer chromatography. This elimi-
nates the need for special applicators and glass plates of specific dimensions,
and the prolonged development periods. It also permits quantitative recovery
of the components and their spectroscopic determination.
3. Apparatus
Micropipettes
Test tubes
4. Materials
a-Alanine Isoleucine Silica gel G
Aspartic acid Ninhydrin Tyrosine
Glycine
5. Time
2 hours
6. Procedure
a. Coating
The most convenient test-tube size for routine use is 150 mm (length) x 1 4 -
15 mm (external diameter); glass rods should have a diameter of 5 to 10 mm.
The test tubes and glass rods are thoroughly cleaned with a dichromate-
sulfuric acid solution, then with a dilute detergent solution, and are finally
rinsed with water. A homogeneous suspension consisting of one part silica gel
G and 2 parts water is prepared in a test tube or a cylinder. The test tubes (or
rods) to be coated are immersed in the slurry to a depth of 12 cm, removed,
and held for a few seconds above the slurry until draining has almost stopped.
They are then inverted and dried at room temperature for 15 min. The coated
test tubes or rods are activated in an oven at 120 to 130°C for 45 min, cooled,
and kept in a desiccator.
b. Spotting of samples and chromatography

The acids ( 1 - 2 mg/ml water) are applied with a micropipette to the thin layer
1 cm above the closed end of the test tube or rod. The solvent is allowed to
evaporate, and the test tube or rod is lowered carefully into a larger test tube
containing a few ml developing solvent (water-ethanol-acetic acid, 1:5:0.1,
containing 10 mg ninhydrin). After about 30 to 45 mins, the solvent front is
marked with a pencil. The test tube is dried at 110 to 120°C for 10 min,
whereupon amino acids appear as violet and pink spots.
Detection of Amino Acids
Amino Acid Color Rr
Aspartic violet 0.11

Glycine pink 0.31
a-Alanine pink 0.45
Isoleucine pink 0.70
Tyrosine pink 0.73
References
1. Anwar, M. H. (1963). J. Chem. Educ. 40, 29.
2. Hansbury, E . , Ott, D . G . , and Perrings, J . D . (1963). / . Chem. Educ. 40, 31.
3. Rollins, C. (1963). J. Chem. Educ. 40, 32.
4. Peifer, J . J . (1962). Mikrochim. Acta 529.
5. Samuels, S. (1966). J. Chem. Educ. 43, 145.
6. Lie, Κ. B . , and Nyc, J . F . (1962). J. Chromatogr. 8, 75.
7. BeMiller, J . N. (1964). / . Chem. Educ. 4 1 , 608.
8. Ikan, R . , and Rapaport, E . (1967). / . Chem. Educ. 44, 297.
Recommended Review
1. Brenner, M., Niederwieser, Α . , and Pataki, G, (1965). Amino acids and derivatives. In
Stahl, Ε . "Thin-Layer Chromatography," p. 391. Academic Press, New York.
J. Thin-Layer Chromatography of Carbobenzoxy-Peptides

1. Introduction
Thin-layer chromatography of carbobenzoxy (Cbzo) amino acid esters or
diols was reported by Zachau and Karau (1). Erhardt and Cramer (2) and
Pataki (3) have shown that Cbzo-amino acids, Cbzo-peptides, and Cbzo-pep-
tide esters can be separated from each other and from unprotected amino
acids, amino acid ester hydrochlorides, and peptides on silica gel G layers.
In the case of the mentioned solvents, the order of migration is as
follows: Cbzo-peptide esters > Cbzo-peptides > amino acids and peptides.
The course of peptide synthesis using Cbzo compounds can be simply and
rapidly followed by means of this method.
Thin-layer chromatography of Cbzo compounds has been used in the
synthesis of derivatives of oxytocin (4) and other peptides (5). Compounds of
higher molecular weight, e.g., polymyxin, were also chromatographed by this
method (6). Recently, carbobenzoxy amino acids and peptides have been
chromatographed as hydrobromides (7).
II. Amino Acids 283
2. Principle
The procedure outlined below is according to Erhardt and Cramer (2).
3. Apparatus
Thin-layer chromatography equipment
4. Materials
Acetic acid Glycylglycine
Ammonium hydroxide Ninhydrin
n-Butanol Potassium dichromate
Cbzo acids (see table) Pyridine
DL-Alanine Silica gel G
DL-Phenylalanine Sulfuric acid
Glycine
5. Time
2 - 3 hours
6. Procedure
For the preparation of five plates (20 x 20 cm) covered with a coating of
silica gel G 0.25 mm in thickness, 30 g silica gel G and 60 ml water are
required.
b. Development
The following solvents can be used for development:
1. n-Butanol-acetone-acetic acid-ammonia (concentrated
ammonia-water, l:4)-water, 4 . 5 : 1 . 5 : 1 : 1 : 2 , and
2. n-Butanol-acetic acid-ammonia-water, 6 : 1 : 1 : 2 .
The solvents are allowed to rise about 8 to 10 cm in the course of 2 hr.
c. Detection
The plates are dried at 120 to 150°C for 10 to 15 min, and while still hot are
sprayed with a solution of 0.2% ninhydrin in 9 5 % n-butanol and 5 % IN acetic
acid. They are then heated for a few minutes at 120 to 150°C and sprayed with
a saturated solution of potassium dichromate in concentrated sulfuric acid,
whereupon carbobenzoxy derivatives, amino acids, and peptides appear as
dark gray spots.
Detection of Carbobenzoxy-
Peptides
R{ in Solvent
Substance 1 2
Cbzo-Gly 0.81 0.74

Cbzo-Digly 0.66 0.56
Cbzo-Trigly 0.57 0.41
Cbzo-Tetragly 0.51 0.26
Cbzo-Digly-OEt 0.82 0.75
Cbzo-Trigly-OEt 0.76 0.68
Cbzo-DL-Ala 0.77 0.74
Cbzo-DL-Diala 0.72 0.68
Cbzo-DL-Phe 0.74 0.77
Gly-gly 0.17 0.04
DL-Ala 0.27 0.14
DL-Phe 0.45 0.31
Gly 0.22 0.10
References
1. Zachau, H. G . , and Karau, W. (1960). Ber. 93, 1830.

2. Erhardt, E . , and Cramer, F . (1962). / . Chromatogr. 7, 405.
3. Pataki, G. (1964). / . Chromatogr. 16, 553.
4. Huguenin, R . L . , and Boissonnas, R . Α . , (1961). Helv. Chim. Acta 44, 213.
5. Schwyzer, R . , and Dietrich, H. (1961). Helv. Chim. Acta 44, 2003.
6. Volger, K . , Studer, R . O., Legier, W . , and Lanz, P. (1960). Helv. Chim. Acta 43, 1751.
7. Maskaleris, M. L . , Sevendal, E . S., and Kibrick, A . C. (1966). J. Chromatogr. 23, 403.
K. Questions
1. What are the three general classes into which the naturally occuring
amino acids may be divided? Illustrate by examples.
2. What is a zwitterion? What is meant by an isoelectric point? How is it
related to the solubility of an amino acid?
3. Write equations for the appropriate preparation of the following
compounds: a. alanine, from propionic acid; b. valine, using the
Strecker synthesis; c. leucine, using the Gabriel synthesis.
4. Review the methods for the preparation of α-amino acids.
5. Outline the steps in the resolution of a racemic amino acid.
6. Show how L-leucine could be converted into D-leucine.
III. Nucleic Acids 285
7. What are essential amino acids?

8. Explain and illustrate by examples the processes of deamination and
transamination of amino acids.
9. Describe the biosynthetic pathways of glycine and serine, and of
phenylalanine and tyrosine.
10. What are peptide antibiotics and hormones? Give examples.
11. Describe the methods generally used for the fractionation of peptides.
L. Recommended Books
1. Bernfeld, P. (1963). "Biogenesis of Natural Compounds." Pergamon

Press, London, England.
2. Beyerman, H. C., van de Linde, Α., and van den Brink, Maassen,
W., eds. "Peptides, Proceedings of the Eighth European Peptide
Symposium." (1967) Noordwijk, The Netherlands, Sept. 1966.
North-Holland Publ. Co., Amsterdam. The Netherlands.
3. Greenstein, D. M., and Winitz, M. (1961). "Chemistry of Amino
Acids." John Wiley, New York.
4. Meister, A. (1965). "Biochemistry of the Amino Acid" 2 vols.
5. Williams, R . M. (1989). "Synthesis of Optically Active a-Amino
Acids." Pergamon Press.
III. NUCLEIC ACIDS

A. Introduction
Nucleic acids, originally isolated from cell nuclei, are divided into the follow-
ing two classes according to the nature of the sugar present: the pentose
nucleic acids or ribonucleic acids ( R N A ) , and the deoxypentose nucleic acids
or deoxyribonucleic acids (DNA). Ribonucleic acid is found mainly in the
cytoplasm, while deoxyribonucleic acid is confined to the cell nucleus. Much
information on the structural acids has been obtained through their hydrolysis
by alkalis, acids, and specific enzymes, and the isolation of the hydrolysis
products by the application of paper, column, and thin-layer chromatography
and counter-current distribution extraction.
The pyrimidine bases found in nucleic acids are uracil, thymine, cyto-
sine, 5-methylcytosine, and 5-hydroxymethylcytosine.
OH OH NH2
CH,
Ν
HCAN- HO^N HO-^N^

Uracil Thymine Cytosine
NH NH,
CH,OH
Ν
HO "N'
5-Methylcytosine 5-Hydroxymethylcytosine
The purine bases present are adenine and guanine
NH2 Η
Guanine
Combination of a base with a sugar via a /3-JV-glycoside linkage gives rise

to a nucleoside, e.g., uridine and adenosine.
NH,
ÂN
HOCfto H O C H 2 ο.
Η
HO OH HO OH
Uridine Adenosine
The pyrimidine bases are always attached to the sugar via a nitrogen
at position 1 of the base, while the purine bases are linked via a nitrogen at
position 9 of the base. The pyrimidine nucleosides are much more resistant to
acid than are the purine nucleosides; both nucleosides are stable toward
alkali. Combination of a nucleoside with phosphoric acid produces a nu-

cleotide, e.g., cytidine 3'-phosphate and adenosine 5'-phosphate.
NH, NH2
Ν
Ν > γ ,
V V^N
HO—POCHô
I U-
OH
Ο Η HO OH
I
HO—P=0 Adenosine 5'-phosphate
ι
OH
Cytidine 3-phosphate
Since the ribose nucleosides have three free hydroxyl groups on the
sugar ring ( 2 ' , 3' and 5 ' ) , three monophosphates can be formed. In the case of
deoxyribose nucleosides, the only free hydroxyl groups for phosphate forma-
tion are 3' and 5'.
Many biological compounds have nucleotide structures, e.g., coen-
zymes such as nicotinamide nucleotides, flavine-adenine dinucleotide, and
coenzyme A. Cytidine 5'-triphosphate (CTP) is involved in the biosynthesis
of phospholipids, and guanosine 5'-triphosphate (GTP) in the biosynthesis
of proteins.
Acid hydrolysis of RNA forms bases, ribose, and phosphoric acid, while
alkaline hydrolysis forms ribonucleoside 2'- and 3'-phosphates. Hydrolysis in
presence of snake venom diesterase yields nucleoside 5'-phosphate.
The following are the three principal types of RNA found in living cells:
6
ribosomal (rRNA), found in ribosomes, molecular weight 0 . 5 - 2 . 0 x 1 0 ;
soluble or transfer R N A (sRNA), molecular weight about 25,000; and mes-
6
senger RNA (mRNA), molecular weight ^ 0 . 5 x 1 0 .
The main internucleotide linkage in RNA is the phosphoester group
connecting C-5' of one nucleotide with C-3' of the next.
Todd and his coworkers have shown that alkaline hydrolysis of nu-
cleotides yields nucleoside 2'- and 3'-phosphates. Acid treatment of these
phosphates forms the cyclic nucleoside 2',3'-phosphate; on hydrolysis of the
latter a mixture of 2'- and 3'-phosphates is obtained.
HOCH
\H m
m—ΤΗ
Ο OH Ο Ο
0=Ρ-ΟΗ
/
o-V HOCH
^ Alkali /
/
Η Η,
Η Η
H2Çô^R
Ο Ο
Η
Η Η,
Η TÛT 0=Ρ-ΟΗ
Ο ΟΗ
οο
0=Ρ-ΟΗ
Ο
/ ο-Υ HOCH
Η Η
HOCH 2 ο
H,C
/
Λ R, ο Η Η
ΟΗ Ο
Η
H . C O R, Ο ΟΗ
Η\ Η Ρ03Η2 Ρ03Η2
Ο ΟΗ Ο ο
0=Ρ-ΟΗ
I
0-V
I I
ΟΗ ΟΗ
Hydrolysis of a trinucleotide by alkali. R represents a purine or
a pyrimidine base
The polynucleotide chains are now represented in a schematic way as follows:
Base Base Base Base
where the vertical line denotes the carbon chain of the sugar with the bases
attached at Q ; each phosphate group bridges the 3'-hydroxyl group of one
pentose ring and the 5'-hydroxyl of the next.
DNA exists in the cell nucleus as deoxyribonucleoprotein; the molecu-
6 9
lar weight of DNA ranges from 1 0 to 10 . The internucleotide bond in DNA,
like that in RNA, is the 3',5'-phosphodiester linkage. The absence of a
hydroxyl group at C-2' makes cyclic phosphate formation impossible, and
DNA thus differs from RNA in that it is not hydrolysed by alkali.
Ο
/
0=P—OH
/
Ο
/
H 2C (X Base
Ο Η
/
0=P—OH
/
Ο
/
H 2C Base
Ο Η
/
0=P—OH
/
Ο
/
H 2C O^ Base
Ο Η
0=P—OH
/
Ο
/
H 2C Base
Ο Η
Part of the polynucleotide chain in DNA
Watson and Crick have suggested that the DNA molecule is a double, dextral
helix of two polynucleotide chains winding round the same axis and held
together by hydrogen bonds of the purine and pyrimidine bases (Fig. 4 . 1 ) .
The two phosphate-sugar chains are represented by ribbons and the
pairs of bases holding the chains together are shown as horizontal rods which
form, as it were, the treads of a spiral staircase.
X-ray and enzymatic studies have recently shown that sRNA consists of
a chain of some 70 nucleotides, which is folded back on itself to form a single
loop coiled into a double helix (Fig. 4.2).
Figure 4.1 Diagrammatic representaton of the DNA molecule as proposed

by Watson and Crick.
B. Isolation of Soluble Ribonucleic Acid from Baker's Yeast

1. Introduction
Soluble ribonucleic acid (sRNA) is a mixture of species ranging in molecular
weight from 25,000 to 30,000 (75 to 100 nucleotides). Three methods have
been used to isolate sRNA. In the first method the tissue is disintegrated and
nuclei and microsomal particles are removed by high-speed centrifugation,
leaving sRNA in the supernatant liquid which is extracted with phenol.
Isolation of sRNA from Escherichia coli using this method was described by
Tissieres ( 1 ) , and from rabbit liver by Cantoni and colleagues (2). The second
method involves the direct extraction of nucleic acids from the tissues, and
subsequent separation of sRNA from rRNA. Extraction of whole cells with
phenol yields a mixture of nucleic acids, from which sRNA is extracted with
cold sodium chloride. Dirheimer (3) separated sRNA from rRNA by chroma-
tography on Sephadex G-200. The third method calls for the direct extraction
Figure 4.2 Schematic representation of the helical structure of the sRNA

molecule. C, cytidine; A, adenosine; G, guanosine; p, phosphate.
of yeast cells with phenol (4, 5 ) . The cells are not broken, and their walls
permit the passage of RNA of low molecular weight into the extracting
liquid. This method is particularly suitable for large-scale preparations of
sRNA (6, 7 ) .
The sRNA isolated by the above methods is usually contaminated by
polysaccharides, which can be removed by extracting the nucleic acid from
1.25 M potassium phosphate (pH 7.5) with 2-methoxyethanol, followed by
precipitation with ethanol and dialysis (8). The removal of the contaminating
rRNA and polysaccharides has been effected with D E A E (diethylamino-
ethyl)-cellulose columns (9).
2. Principle
In the following procedure (7), baker's yeast is treated with aqueous phenol,
which precipitates protein and DNA. The aqueous layer obtained on centri-
fugation contains RNA and polysaccharides. Both are precipitated by etha-
nol. sRNA is extracted with a buffer and purified by column chromatography
on DEAE-cellulose, which removes the contaminating polysaccharides.
3. Apparatus
Stirrer
4. Materials
Baker's yeast Ethanol Potassium acetate
DEAE-cellulose Phenol fWs-HCl buffer
5. Time
3 - 4 hours
6. Procedure
a. Isolation of sRNA
Baker's yeast (15 g) is mixed thoroughly with 14 ml 8 8 % phenol and 33 ml
water, and left to stand for 1 hr with occasional stirring. The mixture is then
placed in a 50-ml tube and centrifuged at 10,000 rpm for 12 min. About 25 ml
of the aqueous supernatant is collected by means of a rubber bulb attached to
a suitable pipette. Phenol (1.5 ml, 8 8 % ) is added to the yeast extract, with
stirring, and again centrifuged as before. The upper phase is separated as
above, and 0.25 ml 2 0 % aqueous potassium acetate (pH 5.2) and 50 ml 9 5 %
ethanol are added to precipitate crude sRNA. Equal portions of the prepara-
tion are then introduced into two 50-ml centrifuge tubes, allowed to stand for
5 min, and then centrifuged as above. The supernatant liquid is decanted, and
the residue is transferred to a 15-ml tube by washing it from the larger tubes
with small amounts of 9 5 % ethanol. After centrifugation, ethanol is de-
canted, and the sRNA is dissolved in 3 ml 0.1 M tris-HCl buffer (pH 7.5) for
column chromatography.
b. Preparation of DEAE-cellulose column

One g DEAE-cellulose is stirred with 40 ml 0.1 M irä-HCl buffer, and the
slurry is poured into a 1 x 10 cm tube. The liquid is poured into the top of the
column, 40 ml buffer is added, and the liquid is allowed to percolate at a flow
rate that should not exceed 1 ml per min.
c. Chromatography of sRNA
The solution of sRNA is added to the column and allowed to pass through the
cellulose. The column is then washed with 40 ml buffer. The sRNA is precipi-
tated from the eluate by the addition of 3 volumes of ethanol ( 9 5 % ) and
separated by centrifugation. This operation is repeated, and the sRNA is
allowed to dry at room temperature.
References
1. Tissieres, A. (1959). / . Mol. Biol. 1, 365.

2. Cantoni, G. L . , Gelboin, H. V . , Luborsky, S. W., Richards, H. H., and Singer, M. F .
(1962). Biochim. Biophys. Acta 61, 354.
3. Dirheimer, G . , Weil, J . H., and Ebel, J . P. (1962). Compt. Rend. Acad. Sei. 255, 2312.
4. Monier, R . , Stephensen, M. L . , and Zamecnik, P. (1960). Biochim. Biophys. Acta 43, 1.
5. Osawa, S. (1960). Biochim. Biophys. Acta 43, 110.
6. Monier, R . (1962). Bull. Soc. Chim. Biol. 44, 109.
7. Holley, R . W. (1963). Biochim. Biophys. Res. Commun. 10, 186.
8. Kirby, K. S. (1956). Biochem. J. 64, 405.
9. Holley, R . W., Apgar, J . , Doctor, B . P., Farrow, J . , Marini, W. Α . , and Merrill, S. H.
(1961). / . Biol. Chem. 236, 200.
Recommended Reviews
1. Brown, L. Preparation, fractionation and properties of sRNA. In "Progress in Nucleic Acid
Research" ( J . N. Davidson, and W. E . Cohn, eds.), Vol. 2, p. 259. Academic Press, New
York.
2. Kirby, K. S. (1964). Isolation and fractionation of nucleic acids. In "Progress in Nucleic Acid
Research" ( J . N. Davidson, and W. E . Cohn, eds.), Vol. 3, p. 1. Academic Press, New Y o r k .
II. Nucleic Acids 293
C. Preparation of Thymidine 3-Phosphate

1. Introduction
Many reagents have been employed for the synthesis of phosphate esters (1).
Multifunctional reagents, e.g., phosphorus oxychloride ( 2 , 3 ) and polyphos-
phoric acid ( 4 ) , are of limited value because of the complex mixture of
products they produce; their use is practical only when the reaction products
OH
CH,
Ν ^
ο
O^N-
C 6H 5) 3C O C H 2 II DCC
Ο H O P O C H 2C H 2C N Pyridine
I
OH
OH 2-Cyanoethyl phosphate
5'-0-Tritylthymidine
OH OH
CH,
J I
AcOH Ν L Hl O
(C6H5)3COCH2Q HOCH 2 Ο
Ο Ο
I
0=POCH7CH2CN 0=POCH2CH2CN
I I
OH OH
OH
CH,
O^N'
HOCH,
Ο
Ο
I
0=POH
I
OH
Thymidine 3-phosphate
can withstand hydrolysis. Dibenzyl phosphochloridate (5) readily phosphory-

lates most primary alcoholic functions. The benzyl groups can be removed
from the intermediate phosphotriesters by mild catalytic hydrogenolysis using
a palladium catalyst. 2-Cyanoethyl phosphate is converted into an active
phosphorylating agent on reacting with DCC (dicyclohexylcarbodiimide).
The cyanoethyl group is readily eliminated under mild alkaline conditions (6).
Thymidine 3'-phosphate has been prepared by Michelson and Todd (7)
by phosphorylation of 5'-0-tritylthymidine with dibenzyl phosphochloridate,
and by Tener, Khorana, Markham, and Pol (8) with mono-p-nitrophenyl
phosphodichloridate.
2. Principle
2-Cyanoethyl phosphate in the presence of DCC is an active phosphorylating
agent. It breaks down on mild alkaline treatment, liberating orthophosphate,
H O — Ρ — C H 2C H 2C N H 3 P 0 4 + C H 2= C H C N
OH
while the nucleotides are unaffected under these conditions.
In the following experiment (6), thymidine 3'-phosphate is prepared
using 2-cyano-ethylphosphate, DCC and 5'-0-tritylthymidine. The crude
product is purified by chromatography and through its barium salt.
3. Apparatus
Stirrer
4. Materials
Acetic acid Hydracrylonitrile
Acetone Lithium hydroxide
Barium acetate Phosphorus oxychloride
Barium hydroxide Phosphorus pentoxide
Benzene Pyridine
DCC Silica gel
+
Dowex 50 [ H ] Thymidine
Ethanol Triphenylmethylchloride
Ether, anhydrous
5. Time
9 days at room temperature

4 hours of laboratory work
6. Procedure
a. Preparation of cyanoethylphosphate
Phosphorus oxychloride (30.6 g [18.4 ml]) is mixed with 200 ml anhydrous
ether in a three-necked flask containing a thermometer, a stirrer, and a
dropping funnel. The solution is cooled to — 10°C in an ice-salt bath, and a
mixture of 15.8 g anhydrous pyridine (16.1 ml) and 14.2 g hydracrylonitrile is
added dropwise, with vigorous stirring, during 1 hr. Stirring is then continued
for an additional hour at - 1 0 ° C . The mixture is poured slowly, with stirring,
into a mixture of 750 ml water, 80 ml pyridine, and 300 g ice. Barium acetate
(100 g) in 300 ml water is added to this mixture, and it is set aside for 2 hr.
The precipitated barium phosphate is filtered on a Büchner funnel. The ether
is evaporated, and two volumes 9 5 % ethanol are added slowly, with stirring,
to the clear filtrate. After 1 hr at 0°C, the plates of barium salt are collected
and washed first with 5 0 % ethanol and then with pure ethanol; yield, 41 g.
A standard solution containing 1 mmole/ml for use in phosphorylations
is prepared as follows: 16.1 g dried barium salt is dissolved in water (Dowex
+
50 [ H ] is added to aid solution) and washed through a column of Dowex 50
+
[ H ] resin; 20 ml pyridine is added to the effluent, and the solution is
concentrated in vacuo to about 20 ml, transferred to a 50-ml volumetric flask,
and diluted to the mark with pyridine. This reagent is stable for 1 month.
b. Preparation of 5'-0-tritylthymidine
Triphenylmethylchloride (3.5 g) is added to a solution of 2.5 g anhydrous
thymidine in 50 ml dry pyridine, and the mixture is left at room temperature
for 1 week. It is then cooled to 0°C and poured into 500 ml ice-water with
vigorous stirring. The precipitate obtained is washed with water and dried in
vacuo over phosphorus pentoxide. The product is then dissolved in 5 ml
acetone and 35 ml dry benzene. After filtration, the acetone is distilled and
the resulting solution is cooled. 4 g 5'-0-tritylthymidine separate as colorless
needles, mp 128°C. [α]Ό + 19.2° (in ethanol, 9 5 % ) .
c. Thymidine-3'-phosphate
A solution of 560 mg 5'-0-tritylthymidine and 2 ml 2-cyanoethyl phosphate
standard solution in 20 ml pyridine is concentrated to dryness in vacuo at
30°C. The residue is taken up in 20 ml dry pyridine and again concentrated to
drynesss. This process is repeated a second time to ensure removal of water.
Finally, the residue is dissolved in 10 ml dry pyridine, and 1.67 g D C C is
added. The reaction mixture is left in a well-stoppered flask for 2 days at room
temperature, during which time dicyclohexylurea separates. One ml water is
then added, and after an hour at room temperature the solution is concen-
trated to dryness in vacuo. The residue is treated with 30 ml 1 0 % acetic acid
at 100°C for 20 min and concentrated to dryness. The last traces of acetic acid
are removed by a second evaporation after adding 20 ml water. The residue is

next treated with 40 ml 0.5N lithium hydroxide at 100°C for 45 minutes. The
reaction mixture is cooled and the precipitate is removed by centrifugation.
The supernatant is then passed through a column (2 x 20 cm) of Dowex 50
+
[ H ] resin, and the effluent is adjusted to pH 7.5 with barium hydroxide. The
solution is concentrated in vacuo to about 15 ml and filtered to remove traces
of impurity, and the barium thymidine 3'-phosphate is precipitated by the
addition of two volumes of ethanol. The precipitate is collected by centrifuga-
tion and washed with 5 0 % ethanol followed by ethanol, acetone, and ether.
Finally it is dried over phosphorus pentoxide; yield, 450 mg ( 8 8 % ) .
References
1. Cramer, F . (1960). Angew. Chem. 72, 236.
2. Chambers, R . W., Moffat, J . G . , and Khorana, H. G. (1957). J. Am. Chem. Soc. 79, 3747.
3. Michelson, A. M., and Todd, A . R . (1949). / . Chem. Soc. 2476.
4. Hall, R . H., and Khorana, H. G . (1956). / . Am. Chem. Soc. 78, 1871.
5. Atherton, F . R . , Openshaw, H. T . , and Todd, A. R . (1945). / . Chem. Soc. 382.
6. Tener, G. M. (1961). J. Am. Chem. Soc. 83, 159.
7. Michelson, A . M L , and Todd, A. R . (1953). / . Chem. Soc. 951.
8. Tener, G. M., Khorana, H. G . , Markham, R . , and Pol, E . H. (1958). J. Am. Chem. Soc.
80, 6223.
Recommended Reviews
1. Brown, D . M. (1963). Phosphorylation. In "Advances in Organic Chemistry(R. A.
Raphael, E . C. Taylor, and H. Wynberg, eds.), Vol. 3, p. 75. Interscience, New York.
2. Todd, A . R . (1957). Chemical synthesis of nucleosides and nucleotides. In "Advances in
Enzymology'," (S. P. Colowick, and N. O. Kaplan, eds.), Vol. 3, p. 822. Academic Press,
New York.
D. Chemical and Enzymatic Preparation of Cyclic Nucleotides
Ribonucleoside cyclic phosphates are the 2',3'-monophosphate esters of nu-

cleosides. Two methods are generally used for the preparation of cyclic
nucleotides: degradation of substances containing phosphodiester struc-
tures, and dehydration of nucleotides.
1. Introduction
a. Synthesis of uridine 2',3'-cyclic phosphate
The ribonucleoside 2',3'-cyclic phosphates were synthesized by Brown, Mag-
rath, and Todd (1) by treatment of the 2'(3')-nucleotides with trifluoroacetic
anhydride; better yields were obtained by Crooks, Mathias, and Robin (2).
Khorana and his coworkers ( 3 , 4 ) have obtained high yields by the reaction of
the nucleotides with DCC in aqueous pyridine.
Other methods reported to give high yields are those of Michelson (5)
involving the reaction of tri-n-octylamine or tri-n-decylamine salts of the
nucleotides with tetraphenylphosphate or diphenylphosphochloridate in diox-
ane. By treatment of the nucleotide and a base with ethyl chloroformate in an
aqueous or anhydrous medium ( 6 ) , Smith, Moffat, and Khorana (7) have
prepared cyclic phosphates by reaction of the ammonium salts of the nu-
cleotides with D C C in aqueous tert-butyl alcohol and formamide, Ukita and
Irie by reaction of the pyridine salts of the nucleotides with D C C in an
anhydrous medium (8).
b. Enzymatic preparation of cyclic nucleotides

Jones (9) was the first to use pancreatic ribonuclease for the digestion of yeast
RNA. It was purified and crystallized by Kunitz in 1940 and named ribonu-
clease (10). It has no action on DNA and is strongly antigenic. The main action
of ribonuclease is to split the linkage joining the phosphate residue at C-3' in
a pyrimidine nucleotide to C-5' in the next nucleotide sequence. If the
enzyme acts on R N A for a short time, the main products are the cyclic
2',3'-phosphates. They are slowly hydrolyzed by the ribonuclease to yield
pyrimidine 3'-phosphates.
Enzyme activity may be determined spectrophotometrically (11), mano-
metrically (12), and by other methods (13).
2. Principle (synthesis)
The following method (14) is based on dehydration of the monophosphates
such as uridine 2'(3')-phosphate with D C C in dimethylformamide.
HOCH2 - H 20
HOCH2
Ο :o
ο
HO ο Ο
\ /ο
HO-P=0 Ρ
/ ^
OH HO ο
Undine 2-phosphate
Uridine 2',3'-cyclic phosphate
3. Apparatus
Centrifuge
4. Materials
Barium acetate
Dimethylformamide
DCC
Uridine 2'(3')-phosphate
5. Time
2 - 3 hours
6. Procedure
To 100 mg uridine 2'(3')-phosphate and 400 mg DCC in a 100-ml flask is
added 8 ml dimethylformamide. All the solid material dissolves rapidly on
gentle swirling of the contents. After a few minutes the solution becomes
cloudy and a precipitate appears. Approximately 40 ml water is added to the
reaction mixture; the resulting pH is about 4. The mixture is passed through a
fritted-glass filter, and the precipitate is washed with 5 ml water. The com-
bined filtrates are neutralized by the careful addition of about 3 ml O.liV
sodium hydroxide, and evaporated under reduced pressure (water pump)
until only a little dimethylformamide remains. Acetone is then added to
precipitate the uridine 2',3'-phosphate as a powder and to extract the residual
dimethylformamide and cyclohexylureas. This step is repeated several times,
and the acetone is removed each time by decanting and pipetting. The
resulting sodium salt may be left under acetone and is stable for several
months in the deep freeze. Alternatively, the acetone may be removed from
the sodium salt in a stream of air, or under reduced pressure, and the residue
taken up in about 2 ml water. The barium salt may then be precipitated by the
addition of triethylamine to pH 9 and the addition of 1 ml 1 M barium acetate,
followed by 3 volumes of ethanol. The precipitate is centrifuged (or filtered),
washed with ethanol followed by ether, and dried in vacuo over phosphorus
pentoxide.
7. Principle (enzymatic degradation)

Yeast RNA is degraded by pancreatic ribonuclease (15). Cyclic nucleotides
diffuse out of the dialysis bag, and the solution is concentrated and subjected
to descending paper chromatography; the cyclic nucleotides form the lowest
band.
8. Apparatus
Dialysis bag
Paper chromatography chamber
9. Materials
Dialysis cellophane bag
Isopropanol
Pancreatic ribonuclease
Yeast RNA
10. Time
4 hours
11. Procedure
Pancreatic ribonuclease (100 ^ g ) is added to a solution of yeast R N A (500 mg
in 10 ml adjusted to pH 7 ) , and the mixture is placed in a cellophane dialysis
bag in a large volume of distilled water. The dialysate is collected at intervals
and concentrated in vacuo. It is then chromatographed, together with some
reference substances, on Whatman No. 3 MM paper in a solvent consisting of
isopropanol (70 parts), water (30 parts), and 0.35 ml ammonia solution (sp gr
0.88). The solvent is allowed to flow until the lowest band almost reaches the
bottom of the sheet (descending technique). The compounds are detected by
viewing the bands at 254 ιημ.
References
1. Brown, D . M., Magrath, D . J . , and Todd, A . R . (1952). J. Chem. Soc. 2708.
2. Crooks, Ε . M . , Mathias, A . P., and Robin, B . R . (1960). Biochem. J. 74, 230.
3. Dekker, C. Α . , and Khorana, H. G. (1954). J. Am. Chem. Soc. 76, 3522.
4. Tener, G . M . , and Khorana, H. G . (1955). / . Am. Chem. Soc. 77, 5349.
5. Michelson, A . M. (1958). Chem. Ind. (London) 70.
6. Michelson, A . M. (1959). / . Chem. Soc. 3665.
7. Smith, M . , Moffat, J . G . , and Khorana, H. G. (1958). / . Am. Chem. Soc. 80, 6204.
8. Ukita, T . , and Irie, M. (1960). Chem. Pharm. Bull. (Tokyo) 8, 81.
9. Jones, W. (1920). Am. J. Physiol. 52, 203.
10. Kunitz, M. (1940). / . Gen. Physiol. 24, 15.
11. Dickman, S. R . , Aroskar, J . P., and Kropf, R . Β . (1956). Biochim. Biophys. Acta 2 1 , 539.
12. Zittle, C. Α . , and Reading, Ε . Η. (1945). J. Biol. Chem. 160, 519.
13. Scheraga, Η. Α . , and Rupley, J . A. (1962). Advances in Enzymology 24, 161.
14. Czer, W., and Shugar, D . (1963). Biochem. Prepns. 10, 139.
15. Markham, R . , and Smith, J . D . (1952). Biochem. J. 52, 552.
Recommended Reviews
1. Khorana, H. G . (1961). Cyclic phosphate formation and its role in the chemistry of phosphate
esters of biological interest. In Khorana, H. G. "Some Recent Developments in the Chemistry
of Phosphate Esters of Biological Interest," p. 44. John Wiley, New York.
2. Markham, R . (1957). The preparation and assay of cyclic nucleotides. In "Advances in
Enzymology" (S. P. Colowick, and N. O. Kaplan eds.), Vol. 3, p. 805. Academic Press,
New Y o r k .
E. Ion-Exchange Thin-Layer Chromatography of Nucleotides

1. Introduction
In recent years, special, finely powdered cellulose cation- and anion-exchange
materials have been developed and used in thin-layer chromatography. Thus,
Randerath has used ECTEOLA-cellulose (1) (obtained by treating sodium
cellulose with epichlorhydrin and triethanolamine) and PEI-cellulose
(poly(ethyleneimine)-impregnated cellulose) (2) for the separation of nucleic
acid derivatives on thin layers. The application of D E A E (diethylami-
noethyl)-cellulose (3) and DEAE-Sephadex (4) was recently reported. It is
noteworthy that sharp and rapid separations of very small amounts of nu-
cleic acid derivatives (0.05-1 ^tg) have been obtained on ion-exchange thin
layers.
The procedure outlined below is based on that of Randerath (5).
2. Apparatus
Electric mixer
T L C applicator
3. Materials
Cellulose powder
Nucleotides
Polyethyleneimine hydrochloride
4. Time
Overnight drying of T L C plates
3 hours
5. Procedure
A dialyzed 1% P E I hydrochloride solution is prepared from a 10%
poly(ethyleneimine) hydrochloride solution, pH about 6.0, and dialyzed
against distilled water. A suspension of 30 g cellulose powder for thin-layer
chromatography in 200 ml dialyzed solution is homogenized in an electric
mixer for about 30 sec. Glass plates (10 x 20 or 20 x 20 cm) are then covered
by means of an applicator to a thickness of 0.5 mm. The plates are then dried
overnight at room temperature. The resulting layers have a capacity of
approximately 1.5 mEq nitrogen per gram cellulose. Layers of lower capacity
can be prepared in the following manner without previous dialysis of the PEI
solution. 10 g 5 0 % P E I solution are diluted with 700 ml distilled water,
brought to pH 6 with concentrated hydrochloric acid, and finally made up to
1 liter with distilled water. Cellulose powder (30 g) is suspended in 200 ml

P E I solution, and the plates are coated with an applicator and allowed to dry
overnight at room temperature. These layers have a capacity of 0.7 to
0.8 mEq nitrogen per gram cellulose.
b. Chromatography
The samples are applied at a starting line, drawn with a soft pencil, 3 cm from
the lower edge of the plate. Sodium or lithium salts of nucleotides (0.002M
solutions) in distilled water are used. After spotting, the plates are exposed to
a current of cold air for about 3 min. Ascending chromatography is carried
out in closed tanks filled with solvent to a height of 0.7 to 1.0 cm. All
chromatograms are developed up to a dividing line 10 cm above the starting
line. The elution is carried out perpendicular to the coating direction. The
development time ranges from 40 to 65 min, depending on the composition of
the solvent. The plates are then dried in a stream of hot air. The compounds
are located by examining the plates in incident shortwave ultraviolet light and
marked on the plate with a pencil.
It is possible to separate interfering substances from nucleotides by a
preliminary development with distilled water. Under these conditions, all
nucleotides, with the sole exception of DPN, remain at the origin, while all
water-soluble basic or neutral compounds migrate. The second development
with electrolyte solutions, in order to separate the nucleotides, can be carried
out either in the direction of the first development or, preferably, perpendic-
ular to it.
Although ion-exchange chromatography is less sensitive than partition
chromatography to the presence of salts in the samples to be analyzed, a large
excess of undesirable anions does seriously interfere with the separations on
PEI-cellulose layers. Interfering salts can be removed as follows: the samples
are spotted in the usual manner, and the plates, after drying in a stream of air,
are laid in a flat dish for about 10 min with anhydrous, reagent-grade metha-
nol (300-600 ml). The layers are then dried, and chromatography is carried
out as described above.
c. Elution under neutral conditions

At neutral pH, the rate of migration of nucleotides with the same base de-
creases in the following order: nucleotide sugars > monophosphates >
diphosphates > triphosphates (see the following table).
d. Stepwise elution
A mixture of DPN, A D P G , AMP, A D P , and ATP cannot be resolved
with one and the same solvent, since the differences in the adsorption affini-
ties of these compounds for PEI-cellulose are too great. In such a case the
/?, Values of Nucleotides at Neutral pH
Solvent: LiCl in Water

0
Compound 1.0 M 1.6 M
5-AMP 0.52 0.65

5'-IMP 0.59 0.74
5'-GMP 0.40 0.51
5'-CMP 0.64 0.75
5'-UMP 0.74 0.80
ADP 0.26 0.54

IDP 0.30 0.63
GDP 0.17 0.45
CDP 0.33 0.64
UDP 0.41 0.71
ATP 0.06 0.34

ITP 0.09 0.39
GTP 0.05 0.25
CTP 0.11 0.41
UTP 0.14 0.49
° A , adenosine; G , guanosine; I, inosine;

C, cytidine; U , uridine; M, mono; D , di;
T , tri; Ρ, phosphate.
chromatogram is developed with a series of solvents of increasing electrolyte

concentration.
The discontinuous, stepwise procedure used for elution involves three
transfers of the plate, without intermediate drying, from one tank to another
containing a higher LiCl concentration. As compared with elution at constant
concentration, development with increasing concentrations gives sharper and
more circular spots. For the separation of adenine and uracil nucleotides on a
0.5-mm thick PEI-cellulose layer, the plate is developed for 1 min with 0.1M
LiCl, for 5 min with 0.3M LiCl, for 15 min with 0.7M LiCl, and for 25 min
with 1.5M LiCl. Developing distance, 10 cm; time, 45 min.
The choice of the solvent depends on the composition of the mixture to
be analyzed; for example, if the mixture contains only nucleotide sugars and
nucleoside monophosphates, LiCl molarities between 0.1 and 1.0 are suit-
able. If a mixture of nucleoside di- and triphosphates is to be analyzed, the
concentration range would be between 0.6 and 0.8M for the first solvent and
1.7 and 2.0M for the last solvent. In most cases, two to five steps are
sufficient.
References
1. Randerath, Κ. (1961). Angew. Chem. 73, 436.
2. Randerath, Κ. (1962). Biochim. Biophys. Acta 6 1 , 852.
3. Dyer, T . A . (1963). J. Chromatogr. 11, 414.
4. Weiland, T . , Lüben, G . , and Determann, H. (1962). Experientia 18, 430.
5. Randerath, K . , and Randerath, E . (1964). / . Chromatogr. 16, 111.
F. Questions
1. Define nucleoside and nucleotide and give an example of each.

2. What is the main structural difference between RNA and DNA?
3. Describe the Watson-Crick representation of DNA.
4. Compare RNA and DNA with respect to acidic and alkaline
hydrolysis.
5. Describe the methods for the isolation of nucleic acids.
6. What is the biological function of sRNA?
7. Describe the nucleic acids of viruses.
8. What are nucleases, their sources, and functions in nucleic acids?
9. What is meant by a replication of DNA? Describe an experiment
showing such a replication by multiplying bacteria.
10. Describe in detail the transfer of genetic information.
G. Recommended Books
1. Allen, F. W. (1962). "Ribonucleoproteins and Ribonucleic Acids."

Elsevier, Amsterdam, The Netherlands.
2. Ayad, S. R . (1972). "Techniques of Nucleic Acid Fractionation."
Wiley-Interscience, New York.
3. Chargaff, E . (1963). "Essays on Nucleic Acids." Elsevier,
4. Chargaff, E . , and Davidson, J . N., (eds.) (1955). "The Nucleic
Acids." Academic Press, New York.
5. Davidson, J . N. (1965). "The Biochemistry of the Nucleic Acids."
Methuen, London. England.
6. Gerhke, C. W., and Kuo, K. C. T. (1990). "Chromatography and
Modification of Nucleosides." Elsevier, Amsterdam, The
Netherlands.
7. Jordan, D. O. (1960). "The Chemistry of Nucleic Acids."
Butterworth, London. England.
8. Khorana, H. G. (1961). "Some Recent Developments in the
Chemistry of Phosphate Esters of Biological Interest." John Wiley,
New York.
9. Michelson, A . M. (1963). "The Chemistry of Nucleosides and

Nucleotides." Academic Press, London. England.
10. Pullman, B . , and Jortner, J . , (1983). "Nucleic Acids: The Vectors of
Life." (eds.) Riedel Publishing Co.
11. Saenger, W. (1983). "Principles of Nucleic Acid Structure."
12. Schimmel, P. R . , Soll, D . , and Abelson, J . N., (1979). "Transfer
RNA: Structure, Properties and Recognition." (eds.) Cold Spring
Harbor Laboratory, Boston, Mass.
13. Townsend, L. B . , ed. (1988). "Chemistry of Nucleosides and
Nucleotides." Plenum, New York.
IV. PORPHYRINS
A. Introduction
Porphyrins are widely distributed throughout the animal and plant kingdoms.
The three most important representatives are hemoglobin, the coloring mat-
ter present in the red corpuscles of blood; chlorophyll, the coloring matter of
green plants and leaves; and the cytochromes, the redox enzymes. The
functions of these substances differ. Hemoglobin participates in oxidative
reactions, while chlorophyll acts as an intermediary in the photosynthetic
process of reduction of atmospheric carbon dioxide to carbohydrates, and
cytochromes promote cellular respiration.
Porphyrins have the property of combining very readily with a variety of
metals to form metalloporphyrins. Thus, vanadium porphyrin complexes
have been identified in shale oils, and a copper uroporphyrin constitutes
CH2
COOH COOH
Heme
IV. Porphyrins 305
the red coloring matter of the wings of certain birds. Many complexes of por-
phyrins with iron, magnesium, zinc, manganese, cobalt, nickel, silver, tin,
and cadmium have been prepared. Among these, the hemes are the most
important.
Hemoglobin is a conjugated protein made up of a prosthetic group, the
heme, and a protein part, the globin, in the proportion of 1 part heme to 26
parts globin. On treatment of hemoglobin with hot sodium chloride and acetic
acid, it is decomposed to hemin, the red coloring matter. Treatment of hemin
with dilute acid results in the removal of iron, thus yielding protoporphyrin.
Vigorous reduction of hemin with hydriodic acid and acetic acid causes its
degradation into four pyrrole derivatives.
H,C H 3C . C 2H 5
H 3 CT ^ N " CH3
ι
H H
Hemopyrrole Kryptopyrrole
Xx
H5 C 2v
2"5
CH3
I
Η Η
Phyllopyrrole Opsopyrrole
Reduction of hemin with tin and hydrochloric acid affords four pyrrole
hemocarboxylic acids.
Oxidation of hemin with chromic acid gives hematinic acid; reduction of
hemin and oxidation of the resulting mesoporphyrin gives hematinic acid
together with ethylmethylmaleimide.
H3C. ^ C H 2 C H 2C O O H H 3C ^ ^ C 2H 5
O ^ N ^ X ) O^TSK X )
I I
Η Η
Hematinic acid Ethylmethylmaleimide
The close chemical relationship between hemin and chlorophyll is illus-

trated by the fact that etioporphyrins are both decarboxylation products of
protoporphyrins and degradation products of chlorophyll.
CH
Ç 2H 5 H CH
X
CH=CH,
2»»5
CH2 Protoporphyrin
COOH
Protoporphyrin
CHjCH, H,C CHXH,
H,C CH,
H i C
H V^c^ / /
'
CH2
2
j HC-C=0
CH2 COOCH3
I
C O O C 2o H 39 Protoporphyrin
Chlorophyll a
Chlorophyll is the green coloring matter present in the chloroplasts of

green plants, especially in their leaves. In the green leaves of higher plants the
chlorophyll content constitutes about 0 . 1 % of the fresh weight. Willstätter
found that the ratio of chlorophyll a to chlorophyll b is remarkably constant,
being about three to one. The molecular formula of chlorophyll a is
C 5 5 H 7 20 5 N 4 M g , and that of chlorophyll b is C 5 5H7o0 6 N 4 Mg. Chlorophyll b
differs from a only by having an aldehyde group instead of a methyl group on
carbon atom 3. The two compounds have different absorption spectra.
IV. Porphyrins 307
Alkaline hydrolysis of chlorophyll a affords the chlorophyllins and two

alcohols—phytol and methanol. Treatment with an ethanolic solution of
oxalic acid yields pheophytin.
COOH
C 3 2H 3 0O N 4 M g / + C 2 0H 3 9O H + C H 3 O H
KOH^/" Chlorophyllin a COOH Phytol Methanol
COOCH3
: 3 2H 3 0O N 4 M g ( ^
Chlorophyll, O
C O C 2 0H 3 9
c COOCH3
« C O O H , 2 X C 3 2H 3 2O N 4 /
C O O C 2 0H 3 9
Pheophytin a
Vigorous treatment of pheophytin with concentrated acids hydrolyzes the

phytyl group, forming pheophorbide.
COOCH3 COOCH3
C 3 2H 3 2O N 4 ^ • C 3 2H 3 2O N 4 ( ^
C O O C 2 0H 3 9 COOH
Pheophytin a Pheophorbide a
When pheophorbide a is hydrolyzed with boiling methanolic potassium

hydroxide, the product is a tricarboxylic acid (chlorin e6).
CH
I
COOH
Chlorin e6
On oxidation with chromic acid chlorin e6 gives hematinic acid and

ethylmethylmaleimide.
Several pigments similar to chlorophyll are known in nature. Bacte-
riochlorophyll, the pigment of purple and brown bacteria, differs from chlo-
rophyll a in the 2-position, where an acetyl residue replaces the vinyl
group, and also contains two additional hydrogen atoms.
C O O C 2 0H 3 9
Bacteriochlorophyll
Protochlorophyll is present in pumpkin seeds and in the rinds of gourds.

Total synthesis of chlorophyll a was accomplished by Woodward and
Strell and their coworkers in 1960.
Cytochromes promote cellular respiration. The well known cytochrome
C is a hemoprotein; its molecular weight is 12.400.
2. Biosynthesis of Porphyrins
The biosynthetic pathway for porphyrins is as follows. Glycine and succinyl-
coenzyme A combine to form the unstable a-amino-/3-ketoadipic acid, which
loses C 0 2 and yields δ-aminolevulinic acid. An enzyme, δ-aminolevulinic acid
dehydrase, promotes condensation of two molecules of the acid, with subse-
quent formation of porphobilinogen.
HOOCH2CH2Cv / C H 2- C O O H
N S K X ; H 2 - N H 2
H
Porphobilinogen
IV. Porphyrins 309
This highly reactive material is readily transformed into a mixture of uro-

porphyrinogens. The latter are decarboxylated to coproporphyrinogen, which
yields protoporphyrin. It is noteworthy that only magnesium and iron have so
far been found in biologically active porphyrins. The introduction of iron to
form heme and other products takes place enzymatically:
Fe + protoporphyrin —» protohem-^ hemoglobin
It is also probable that an enzyme is involved in the insertion of magne-
sium into protoporphyrin:
Mg + protoporphyrin + Mg protoporphyrin-^ chlorophylls
For the formation of chlorophylls, further alterations of side chains are
required, including esterifications and reductions, formation of a cyclopenta-
none ring, and the reduction of one pyrrole ring in case of chlorophyll, or two
pyrrole rings in case of bacteriochlorophyll.
B. Isolation of Hemin from Blood

1. Introduction
The classical method of Schalfejef (1), which was introduced in 1885, involves
slow addition of blood to glacial acetic acid saturated with sodium chloride
at 100°C. The other procedures were developed by Nencki and Zaleski ( 2 ) ,
Piloty ( 3 ) , Fischer (4), and Corwin and Erdman (5). However, the separa-
tion of hemin crystals from a rather viscous solution of proteins in acetic acid
proved to be both tedious and inconvenient. Recently, Chu and Chu (6)
modified the method of hemin isolation by completely removing proteins
before the formation of hemin. For bulk preparations, however, the modified
CH2
CH H CH
cr
Hemin
method of Labbe and Nishida (7) can be used. A micro-scale adaptation of

this method permits crystallization of hemin ( 5 0 % yield) from as little as
0.1 ml blood (8).
2. Principle
In the following procedure (7), hemin is extracted with a mixture of strontium
chloride in acetic acid and acetone. Heating of the extract increases protein
precipitation and hence improves the purity of hemin.
3. Apparatus
Centrifuge
4. Materials
Acetic acid Ethanol Pyridine
Acetone Ether Sodium chloride
Blood Hydrochloric acid Strontium chloride
Chloroform
5. Time
2 - 3 hours
6. Procedure
A stock solution of 2 % strontium chloride hexahydrate in a glacial acetic acid
is prepared. The extraction solvent, composed of one part of this solution to
three parts acetone, is then prepared immediately before use to avoid crystal-
lization of the strontium chloride. One volume blood or similar heme-
containing preparation is added with stirring to 12 volumes extraction solvent.
The mixture is allowed to stand for 20 to 30 min, with occasional stirring.
Brief heating to the boiling point during this period appears to increase
protein precipitation and improves the purity of the hemin. The mixture is
then filtered with gentle suction through a medium-porosity sintered-glass
filter, or by gravity through a coarse filter paper.
The residue is washed twice with one volume of extraction solvent. The
combined filtrate is transferred to a beaker and heated to 100°C. The rate of
concentrating the solution appears to be unimportant; however, in order to
avoid bumping, porcelain chips must be added, and the temperature should
not exceed 100°C. Crystallization of hemin begins as the solution concentrates
and reaches completion when the latter is allowed to cool to room tempera-
ture. The hemin is centrifuged and washed twice with 5 0 % acetic acid and
water and once with ethanol and ether. The yields without further purification
IV. Porphyrins 311
are in the range of 75 to 8 0 % . The crude hemin prepared from 20 ml blood is

recrystallized by stirring with 0.5 ml pyridine. After 5 to 10 min 4 ml chlo-
roform is added, and the solution is filtered. Acetic acid containing 2 %
strontium chloride is added to the filtrate. The solution is then heated to
100°C and allowed to cool. The hemin is then centrifuged and treated as
described above. The overall yield after recrystallization is about 6 0 % .
References
1. Schalfejef, M. (1885). Ber. 18, 232.
2. Nencki, M . , and Zaleski, J . (1900). Z. Physiol. Chem. 3 0 , 390.
3. Piloty, O. (1910). Ann. 3 7 7 , 358.
4. Fischer, H. (1941). Org. Synth. 2 1 , 53.
5. Corwin, A . H., and Erdman, J . G. (1946). / . Am. Chem. Soc. 68, 2473.
6. Chu, T. C , and Chu, E . J . (1955). / . Biol. Chem. 212, 1.
7. Labbe, R . F . , and Nishida, G . (1957). Biochim. Biophys. Acta 26, 437.
8. Formijne, P., and Poulie, N. J . (1954). Koninkl. Ned. Acad. Wetenschap. Proc. Sec. C.
5 7 , 57.
Recommended Review
1. Falk, J . Ε . (1964). "Hems. In "Porphyrins and Metalloporphyrins." Elsevier, Am-
sterdam, The Netherlands.
C. Degradation of Hemin
1. Introduction
The first step in the degradation of hemin involves its conversion to the
iron-free protoporphyrin. In order to remove the iron, it is first reduced to
the ferrous state. If a strong acid is now added, the protons displace the coor-
dinated ferrous ion, forming the porphyrin. The following reducing agents
have been employed: iron powder (1), ferrous sulfate, palladium and hydro-
gen (2), stannous chloride (3), sodium amalgam (4), and hydrobromic acid in
glacial acetic acid (5).
Small samples of protoporphyrin are easiest prepared by treatment
of hemin with ferrous sulfate (6). For work with several grams of hemin,
Grinstein's (7) method can be used. The next step in the degradation is the
catalytic reduction of protoporphyrin to mesoporphyrin, which is carried
out over platinum in formic acid. The mesoporphyrin is oxidized to meth-
ylethylmaleimide (derived from pyrrole rings A and B ) and methyl-/3-
carboxyethylmaleimide or hematinic acid (derived from pyrrole rings C
and D ) . The hematinic acid is then decarboxylated to yield methylethyl-
maleimide, which is ozonized to pyruvic acid and a-ketobutyric acid.
2. Principle
The procedure described below is according to Wittenberg and Shemin (8).
CH2
II
CH H CH3
"V\wCH=CH2
N
H = \ H 2/ P d
Hemin
HCOOH
Protoporphyrin
H5C2 H CH3
H,CV Ί TVC H 2 5
HX
CH, H CH,
CH, CH,
COOH COOH
Mesoporphyrin
COOH
ι
CH2
HX ^C2H5 H 3C I HX --X2H5
CH, NH3
+ C,H,OH
ι + co 2
( Γ ^1*Τ Ό CT ^ N ^ Ό
H Η Η
Methylethylmaleimide Hematinic acid Methylethylmaleimide
IV. Porphyrins 313
Methylethylmaleimide + 0 3 C H 3 C O C O O H + C H 3C H 2C O C O O H
Pyruvic acid α-Ketobutyric acid
3. Apparatus
Ozonator
Sublimation assembly
4. Materials
Ammonium acetate Ethyl acetate Palladium catalyst
Ammonium hydroxide Ferric chloride Petroleum ether
Barium hydroxide Formic acid (100%) Pyridine
Chromic acid Hemin Sodium acetate
Drierite Hydrochloric acid Sodium
Ethanol, absolute Iron, powder bicarbonate
Ethanol, 9 5 % Ozone Sulfuric acid
Ether
5. Time
12-14 hours
Stirring overnight
6. Procedure
a. Conversion of hemin to protoporphyrin
To a boiling solution of 6 g hemin in 300 g formic acid is added 6 g iron
powder in six portions over a period of 30 min. The mixture is stirred for a
further 40 min and filtered. Two to three volumes water saturated with
ammonium acetate are added to the filtrate. The solid material is filtered off,
washed with water, and dried; yield, 4 . 5 - 5 g. It can be recrystallized from
pyridine-water.
b. Conversion of protoporphyrin to hemin

One g finely powdered protoporphyrin is dissolved in 100 ml acetic acid. A
few drops of concentrated hydrochloric acid and 10 ml ferric chloride ( 1 %
solution in 9 0 % acetic acid) are added, the mixture is boiled, and solid
sodium acetate is added portionwise until the solution turns brown and
crystalline hemin starts to precipitate. The mixture is cooled and filtered on a
Büchner funnel, and the residue is washed with acetic acid, water, ethanol,
and ether; yield, 0.9 g.
c. Conversion of protoporphyrin to mesoporphyrin

Protoporphyrin (4.5 g) in 200 ml formic acid (100%) is hydrogenated at
NTP in the presence of a colloidal palladium catalyst ( 1 8 % Pd). After the
hydrogénation is complete, the catalyst is filtered off, and the filtrate is

poured into 3 volumes 3 0 % ammonium acetate to flocculate the mesopor-
phyrin. The product is filtered on a Büchner funnel and washed with water,
and the filtrate is extracted with ethyl acetate. The extract is added to the bulk
of mesoporphyrin. The crude material is dissolved in 2 % ammonium hydrox-
ide and reprecipitated by addition of acetic acid. The collected precipitate is
washed and further purified by dissolving it twice more in ammonium hydrox-
ide and precipitating with acetic acid; yield, 3.5 g.
d. Oxidation of mesoporphyrin to methylethylmaleimide and hematinic acid

A solution of 5.1 g chromic acid in small amount of water is added, with
stirring, over a period of 4 hr to a solution of 2.5 g mesoporphyrin in 170 ml
2 0 % sulfuric acid. Stirring is continued overnight, after which period the
solution turns green. The reaction mixture is diluted with water and extracted
with ether for 4 to 5 hr in a continuous extractor. The ethereal solution
containing methylethylmaleimide and hematinic acid is shaken once with
50 ml 5 % sodium bicarbonate to remove the hematinic acid. The bicarbonate
solution is then extracted six times with equal volumes of ether, and the ether
extracts are combined with the original ethereal solution. The ether is re-
moved by warming, and the residue is sublimed at 70 to 80°C/3 mm; yield,
0.5 g; mp 64-65°C.
The bicarbonate solution is immediately made acid to Congo red paper
with dilute sulfuric acid. After decolorization with a small amount of char-
coal, it is extracted ten times with equal volumes of ether. The ether is
removed in vacuo. The crude hematinic acid (0.65 g) is dissolved in ether and
crystallized by the gradual addition of petroleum ether; mp 114-115°C.
e. Conversion of hematinic acid to C 0 2 and methylethylmaleimide

A suspension of 0.64 g hematinic acid in 10 ml almost saturated ammoniacal
solution of absolute ethanol is heated in a sealed tube for 2 hr at 175°C. The
reaction mixture is then diluted with water and acidified with sulfuric acid,
and the evolving C 0 2 is aerated into barium hydroxide solution. The yield of
barium carbonate is 0.5 g.
After the aeration process, the solution is made alkaline with a dilute
solution of sodium bicarbonate, and immediately extracted six times with
ether. The ether is evaporated, and the residue is acidified and subjected to
steam distillation. The distillate is made slightly acid with dilute sulfuric acid
and extracted with ether in a continuous extractor. The ether solution is dried
over Drierite and evaporated. The product is purified by sublimation; yield,
0.15 g; mp 61-63°C.
f. Ozonization of methylethylmaleimide
Ozonization is carried out by passing ozone through a chloroform solution of
the imide (100 mg in 100 ml chloroform). On concentrating the solution, solid
IV. Porphyrins 315
ozonide is obtained. It is crystallized from a mixture of chloroform and

petroleum ether; mp 83-84°C.
Ozonide (20 mg) is taken up in 50 ml dry ethyl acetate, 10 mg Pd-
C a C 0 3 catalyst is added, and hydrogen is bubbled through the reaction
mixture at NTP for 1 hr. The catalyst is filtered off and washed with ethyl
acetate. The combined ethyl acetate solutions are concentrated in vacuo,
leaving an oily residue, which is tranferred to a tube containing 50 ml satu-
rated aqueous solution of barium hydroxide. The tube is sealed and shaken
continuously at room temperature for 24 hr, after which the solution is
acidified and extracted several times with ether. The solvent is evaporated
in vacuo, and the α-keto acids are converted to the corresponding 2,4-
dinitrophenylhydrazone derivatives. The resulting mixture of the DNPs
of pyruvic and a-ketobutyric acids is separated by paper or thin-layer
chromatography.
References
1. Fischer, H., and Putzer, Β . (1926). Ζ. Physiol. Chem. 154, 39.
2. Lemberg, R . , Bloomfield, Β . , Caiger, P., and Lockwood, W. (1955). Australian J. Exptl.
Biol. 33, 435.
3. Hamsik, A . (1931). Z. Physiol. Chem. 196, 195.
4. Papendiek, A . (1926). Z. Physiol. Chem. 152, 215.
5. Heath, H., and Hoare, D . S. (1959). Biochem. J. 73, 679.
6. Morell, D . B . , Barrett, J . , and Clezy, P. S. (1961). Biochem. J. 78, 793.
7. Grinstein, M. (1947). / . Biol. Chem. 167, 515.
8. Wittenberg, J . , and Shemin, D . (1950). / . Biol. Chem. 185, 103.
Recommended Reviews
1. Falk, J . E . (1964). "Special techniques, in Porphyrins and MetalloporphyrinsElsevier,
2. Rimington, C. R . , and Kennedy, G. Y . (1962). Porphyrins, structure, distribution, and
metabolism. In "Comparative Biochemistry(M. Florkin, and H. S. Mason, eds.), Vol. 4,
D. Thin-Layer Chromatography of Plant Pigments

1. Introduction
In view of the rapidity of thin-layer chromatography, this is a useful technique
for the separation of labile compounds such as chloroplast pigments (chlo-
rophylls a and b and carotenoids). Separations can be carried out by thin-
layer adsorption or partition chromatography. The adsorption technique was
used by Eichenberger and Grob (1) on silica gel G plates, and by Winterstein,
Studer, and Ruegg (2) on thin layers prepared from a mixture of silica gel and
calcium hydroxide, 1:4. This method can lead to the isomerization and
oxidation of the pigments.
Egger (3) has used kieselgur impregnated with triglycerides for the
separation of chlorophylls and their degradation products. Colman and Vish-
niac (4) have used thin layers of sucrose for the separation of leaf pigments.
2. Principle
The procedure outlined below is according to Anwar (5).
3. Apparatus
Thin-layer chromatography equipment
4. Materials
Acetone Glycerine Methanol
Carbon tetrachloride Isooctane Petroleum ether
Celite
5. Time
2 - 3 hours
6. Procedure
a. Extraction of pigments from fresh spinach leaves
The leaves are homogenized in a blender together with sufficient 5 0 % meth-
anol to just cover the leaves. The mixture is centrifuged, and the upper
liquid layer, virtually devoid of pigment, is decanted. The green solids are
mixed with an equal weight of Celite, filtered through a Büchner funnel,
washed with a little acetone, and diluted with water. They are then extracted
several times with petroleum ether and dried over sodium sulfate. The solu-
tion is then filtered, concentrated under reduced pressure, and kept at a low
temperature.
b. Preparation of thin-layer plates

gel G and 50 ml water for 30 sec. It is then spread on the plates with an
applicator to give a layer of 0.25 mm thickness. The plates are activated at
120°C for 30 min.
c. Development
The pigments are spotted by means of micropipettes along a line 2 cm above
the rim of the plate. Development is accomplished with isooctane-acetone-
carbon tetrachloride, 3 : 1 : 1 .
The solvent is allowed to rise about 15 cm above the starting line.
IV. Porphyrins 317
d. Detection
Twelve spots are observed under ultraviolet light and their colors recorded.
Carotenes travel the most rapidly, followed by chlorophyll a and b and
xanthophylls. The spot colors, which are clear and bright at the end of the
development period, fade rapidly and change color on exposure to light and
air. These changes can be delayed for some time by covering the plate with
glycerine. Each color zone is scraped off into a small test tube containing a
few ml solvent and filtered. The ultraviolet spectra are measured in the range
of 400-700 ιημ.
References
1. Eichenberger, W., and Grob, E . C. (1962). Helv. Chim. Acta 45, 974.
2. Winterstein, Α . , Studer, Α . , and Ruegg, R . (1960). Ber. 93, 2951.
3. Egger, K. (1962). Planta 58, 664.
4. Colman, B . , and Vishniac, W. (1964). Biochim. Biophys. Acta 82, 616.
5. Anwar, M. H. (1963). / . Chem. Educ. 4 0 , 29.
Recommended Review
1. Strain, Η. H., and Svec, W. A . (1969). Some procedures for chromatography of the fat-
soluble chloroplast pigments. Adv. Chromatogr. 8, 119.
E. Isolation and Identification of Petroleum Metalloporphyrins

1. Introduction
Crude oil has its origin in the organic debris of plants, algae, bacterial fungi,
and a multitude of microorganisms that have been deposited into aquatic
sediments. A small amount of this organic material ultimately is converted to
fossil fuels. About 9 9 % of the organic material deposited is oxidized, either
chemically or microbially, and recycled into the atmosphere as carbon diox-
ide. Much of the remaining 1% of the material that has been incorporated
into the rocks is further altered, but only a fraction is converted into usable
fossil fuels.
Organic matter that survives oxidation and microbial attack in water
and the initial stages of sedimentation is incorporated into the sediments,
where it undergoes additional alteration and reactions caused by increasing
temperature, or thermal maturation.
Attempts to understand the transformation of organic matter in the
geosphere led to the term biomarkers. Biomarkers are organic compounds,
present in the geospherical record, with carbon skeletons that can be related
to a precursor molecule from a specific type of organism. In essence, bio-
markers are a geochemical fingerprint for an oil or other geological sample
containing organic compounds. Biomarkers commonly used in petroleum
exploration are hydrocarbons, such as n-alkanes, isoprenoids, sesquiter-

panes, di-, tri-, tetra-, and pentacyclic terpanes, steranes, and various aro-
matic hydrocarbons. Biomarker hydrocarbons found in crude oils and
extracts from source rocks generally are derived from oxygenated precursors;
thus, steranes are derived from sterols.
Though it has been known from Treib's work (1936) a half century ago
that metalloporphyrins occur in petroleum and shales and thus are the first
biomarkers derived from chlorophyll and heme, only in the past decade has a
dramatic upsurge in geoporphyrin research occurred. This was attributable
mainly to the advent of mass spectroscopy.
The major metalloporphyrins of petroleum, shales, coals, and bitumens
occur as complex mixtures of Ni and V = 0 complexes of two major skeletal
types D P E P (deoxyphylloerythroetioporphyrin) and Etio (vanadyl etiopor-
phyrin), and three others, Di-DPEP, Rhodo-Etio and Rhodo-DPEP. Por-
phyrins often occur in petroleum around the ppm (parts per million) level
(Fig. 4 . 3 ) .
DPEP-5 Metallo-DPEP Etio-lll
Figure 4.3 In the geosphere, the deoxyphylloerythroetioporphyrins with the

13,15-ethano ring (DPEP-5) and the etioporphyrins (e.g., etio-lll) are major
components, usually as métallo derivatives (e.g., nickel and V = 0 ) . Chlorophyll
a is the putative ultimate biological source for most petroporphyrins.
IV. Porphyrins 319
2. Principle
A sample of crude petroleum (which can be obtained from a geological survey
or a petroleum refinery) is fractionated on a silica gel column. The porphyrin
fractions are detected by their characteristic absorptions in the 550-570 nm
region.
The metalloporphyrins are demetallated by methanesulfonic acid, and
the free porphyrins are determined by measuring their intensity at 618 nm.
The demetallated porphyrins are then separated by HPLC.
Mass spectrometric characterization of the demetallated petroporphy-
rins is performed by direct inlet (probe-insertion) technique.
The method is based on that of Baker, Louda, and Orr (3).
3. Apparatus
Glass column
High pressure liquid Chromatograph
Mass spectrometer
Stainless steel column filled with Partisil
4. Materials
Acetone Hexane Petroleum ether
Alumina Methane sulfonic acid Pyridine
Benzene Methylene chloride Silica gel
Chloroform Pentane Toluene
Ethyl acetate
5. Time
6 hours workup followed by HPLC, GC-MS
6. Procedure
2 g petroleum crude is loaded onto a column (4 x 40 cm) filled with silica gel
in benzene. Elution with benzene (fraction 1) provides a mixture of saturated
hydrocarbons, aromatics, Ni-porphyrins, and nonpolar vanadyl porphyrins.
Solvent polarity is increased to benzene-ethyl acetate ( 2 : 1 , v/v). The major-
ity of vanadyl pigments and N,S,0-containing compounds (i.e., resins) are
collected (fraction 2 ) . At this point the column is flushed with ethyl acetate,
and the eluate (fraction 3) is examined spectrophotometrically ( U V / V I S ) to
assure complete removal of pigments from the adsorbent.
Fraction 1 is dissolved with minimal benzene and loaded onto a col-
umn (2.5 x 30 cm) of silica gel made up in n-pentane. Elution with the fol-
lowing solvents yields these fractions: ( l a ) ^-pentane (saturates and sulfur);
( l b ) ft-pentane-benzene ( 2 : 1 , v/v) (Ni-porphyrins and aromatics); ( l c ) ben-

zene (aromatics); (Id) benzene-ethyl acetate ( 3 : 1 , v/v) (nonpolar V = 0
porphyrins); and ( l e ) ethyl acetate. All fractions are checked via U V / V I S by
monitoring the bands at 550 nm (ε = 34.280) and 570 nm (ε = 26.140) for
nickel and vanadyl porphyrins, respectively.
Crude Ni-porphyrins are then chromatographed over alumina (neutral
grade II-III, 5 - 6 % H 2 0 ) , eluting with 3.5 to 5 % acetone in petroleum ether
(30-60°C). The Ni-porphyrins are demetallated by transferring the solution
background subtraction (using the scans immediately before and after the
appearance of the porphyrins), as considerable amounts of nonporphyrinic
material is present. Note: All operations must be carried out in a hood!
+
Molecular ions assigned to etioporphyrins are M = m/e 3 1 0 + 1 4 n;
+ +
to rhodoporphyrins: M = m/e 358 + 14 n; to DPEP series: M = m/e
308 + 14 n.
References
1. Eglinton, G . , Hajibrahim, S. K . , Maxwell, J . R . , and Quirke, J . M. E . (1980). In "Advances
in Organic Geochemistry." ( A . G. Douglas and J . R . Maxwell, eds.), p. 193. Pergamon
Press, New York.
2. Baker, E . W . , and Louda, J . W. (1986). In "Biological Markers." ( R . B . John, ed.), p. 125.
Elsevier, New Y o r k .
3. Baker, E . W., Louda, J . W., and Orr, W. L. (1987). Org. Geochem. 11, 303.
4. Barwise, A . G. J . , and Whitehead, Ε . V. (1980). In "Advances in Organic Geochemistry.
(A. G. Douglas and J . R . Maxwell, eds.), p. 181. Pergamon Press, New York.
5. Hajibrahim, S. K . , Quirke, J . M. E . , and Eglinton, G. (1981). Chem. Geol. 32, 173.
Recommended Reviews
1. Baker, E . W., and Palmer, S. E . (1978). Geochemistry of porphyrins. In "The Porphyrins."
(D. Dolphin, ed.) Vol. 1, p. 486. Academic Press, New York.
2. Eglinton, G . , Maxwell, J . R . , Evershed, R. P., and Barwise, A. J . G. (1985). Red pigments
in petroleum exploration. Interdisciplinary Science Revs. 10, 221.
3. Louda, J . W., and Baker, E . W. (1986). The biogeochemistry of chlorophyll. In "Organic
Marine Geochemistry," A C S Symp. Ser. (M. L. Sohn, ed.) p. 305.
4. Philp, R . P., and Jung-Nan, Qung. (1988). Biomarkers, Anal. Chem., 60, 887A.
5. Rullkötter, J . (1987). Organic geochemistry. In "Encyclopedia of Physical Science and
Technology," Vol. 6, p. 53. Academic Press, New York.
F. Questions
1. What are the chemical differences between chlorophyll a, chlorophyll

by protochlorophyll, and bacteriochlorophyll?
2. Outline the principal steps in the degradation of hemin.
3. Name some natural metalloporphyrins and their sources.
V. Proteins 321
4. What are the functions of chlorophyll in the photosynthetic process?

5. Compare the biosynthesis of heme and chlorophylls.
6. How are metals inserted into, and withdrawn from, a porphyrin?
G. Recommended Books
1. Bentley, K. W. (1960). "The Natural Pigments." Interscience, New

York.
2. Blauer, G., and Sund, H. (1985). "Optical Properties and Structure of
Tetrapyrroles." W. de Gruyter, New York.
3. Falk, J . E . (1964). "Porphyrins and Metalloporphyrins." Elsevier,
4. Falk, H. (1989). "The Chemistry of Linear Oligopyrroles and Bile
Pigments." Springer-Ver lag, New York.
5. Lasceller, J . (1964). "Tetrapyrrole Biosynthesis and Its Regulation."
Benjamin, New York.
6. Terrien, J . , Truffant, G., and Charles, J . (1957). "Vegetation and
Chlorophyll." Hutchinson, London. England.
V. PROTEINS
A. Introduction
The name protein is derived from the Greek word proteios, meaning primary.
Proteins are high-molecular polypeptides that occur in the protoplasm of all
animal and plant cells. The protein content of tissues varies widely; thus,
blood plasma contains about 7% and egg yolk, about 1 5 % . The following are
the protein contents of seeds of various plants: 2 % in potatoes, 1.6% in beets,
and 1.8% in asparagus. In soy beans, proteins constitute 3 7 % , in peanuts,
2 6 % , and in almonds, 2 1 % . All proteins yield amino acids upon hydrolysis;
acid hydrolysis is preferred, since alkaline hydrolysis causes racemization.
Proteolytic enzymes are often used because they cause neither racemization
nor decomposition of sensitive amino acids. However, their action is
slow. Enzymes are macromolecular catalysts of biological origin. It has been
proved that enzymes are proteins.
They can be classified into four main groups:
Hydrolyzing enzymes (hydrolases), e.g., esterases, peptidases, and ami-
dases, catalyze the cleavage of ester linkage.
"Adding and removing" enzymes (desmolases), e.g., dehydrases,
isomerases, and aldolases, catalyze the addition or removal of some groups
of a substrate, without hydrolysis, oxidation, or reduction.
Transferring enzymes (transferases), e.g., transglycosylases, transami-

nases, and transphosphorylases, catalyze the transfer or shift of a group
from one molecule to another.
Oxidizing and reducing enzymes (oxireductases), e.g., oxidases, aerobic
and anaerobic dehydrogenases, and transelectronases (cytochromes),
catalyze biological oxidations.
Denaturation is one of the most characteristic properties of proteins.

The most important factors governing the rate of denaturation are the
temperature and pH of the solution. Chemical reagents that accelerate de-
naturation are urea, guanidine salts and synthetic detergents, and organic
solvents such as alcohol and acetone. Physical agents are heat, X-rays, ultra-
violet light, and high pressure.
2 +
Protein may be precipitated from solution by a variety of cations ( Z n ,
2 + 2 + 3 + 2 + 2 +
C d , H g , F e , C u , and P b ) and anions (of tungstic, phosphotungs-
tic, trichloroacetic, picric, and tannic acids).
The molecular weights of proteins vary over a wide range: lactalbumin,
about 17,000; gliadin, 27,000; insulin, 38,000; egg albumin, 42,000; hemo-
globin, 68,000; serum globulin, 170,000; edestin, 300,000; and hemocyanin,
6,600,000. The molecular weights of proteins have been determined by means
of osmotic pressure, light and X-ray scattering, viscosity, diffusion, sedi-
mentation in an ultracentrifuge, and by chemical analysis.
The proteins may be classified as follows:
Simple proteins are those that yield only amino acids upon hydrolysis.
1. Albumins are soluble in water and are coagulated by heat. Typical

examples are egg albumin and lactalbumin.
2. Globulins are insoluble in water but are soluble in dilute salt solution.
They are precipitated by half-saturating their solution with ammonium
sulfate, and are coagulated by heat. Typical examples are ovoglobulin,
myosin, arachin, amandin, and serum globulin. Immunoproteins
belong to the γ-globulins and are called antibodies. Their function is
to protect the mammalian body against pathogenic invaders—foreign
proteins, bacteria, or viruses, which are known as antigens. When
antigens penetrate into an organism, the latter responds by forming
antibodies that combine specifically with the antigen. The combination
of large antigen and antibody molecules can be seen under the
electron microscope.
3. Glutelins are soluble in dilute acids and alkalis, and insoluble in
neutral solvents. Typical examples are glutenin of wheat and oryzenin
of rice.
4. Prolamines are soluble in 70 to 8 0 % alcohol, and insoluble in water,
dilute salt solution, or absolute alcohol. Typical examples are zein of
corn, gliadin of wheat, and hordein of barley.
V. Proteins 323
5. Scleroproteins are insoluble in water or salt solution, but are soluble in

strong acids or alkalis. Typical examples are keratins of hair, horns,
and hoofs, elastin of connective tissues, collagen of bones, fibroin and
sericin of silk.
6. Histones are soluble in water and insoluble in dilute ammonia. They
are readily soluble in dilute acids and alkalis. Typical examples are
globin, thymus histone, and gadus histone of codfish sperm.
7. Protamines are the simplest of the proteins. They are basic and yield
mainly basic amino acids upon hydrolysis. The protamines are soluble
in water, dilute ammonia, acids, and alkalis. Typical examples are
salmine of salmon sperm, clupeine of herring sperm, and cyprinine of
carp sperm.
Conjugated proteins are composed of a simple protein combined with

a non-protein group, known as the prosthetic group.
1. Chromoproteins are composed of proteins united with colored
prosthetic groups such as hemoglobin or chlorophyll. Other examples
are cytochromes and flavoproteins.
2. Lipoproteins are formed by combination of proteins with lipids such as
lecithin or fatty acids. They are found in blood, milk, egg yolk, and
the chloroplasts.
3. Metalloproteins are proteins that contain heavy metals such as F e , Co,
Mn, Zn, Cu, Mg, etc. Many enzymes belong to this group.
4. Mucoproteins are composed of proteins and mucopolysaccharides.
They are found in serum, human urine, and albumin.
5. Nucleoproteins are composed of proteins and nucleic acids. The plant
viruses and many of the animal viruses are ribonucleoproteins, since
they consist chiefly of protein and RNA. The tobacco mosaic virus is
the best known nucleoprotein. Its molecular weight is about 40 million,
while that of the influenza virus is 350 million, and that of the
smallpox virus, several billion.
6. Phosphoproteins contain phosphoric acid. They occur in casein and egg
yolk.
Various methods have been developed for determining the sequence
of amino acids in peptides and proteins. Thus, the N-terminal amino acid
sequence can be determined by treatment with 2,4-dinitrofluorobenzene or
phenylisocyanate, and the C-terminal amino acids can be determined by the
formation of a thiohydantoin ring or, preferably, by enzymic cleavage with
carboxypeptidase.
Proteins can be resolved into a mixture of long peptides by controlled
digestion with certain enzymes, e.g., trypsin.
Pauling and Corey have suggested that proteins are arranged in a helix
with 3.7 amino acid residues per turn. Each turn corresponds to a length of
5.4Â in the direction of the long axis of the helix, and each amino acid residue
advances the chain in the direction of the long axis of the helix by 1.5Â. This
helix has been designated the α-helix.
Keratins are the structural proteins of hair, wool, feathers, horn, nails,
and hoofs. Keratin from human hair or wool contains 1 1 - 1 2 % cystine; hence
its great stability, which is due to the large number of — S — S — cross-links
between the peptide chains. Reduction of keratin forms keratin which con-
tains cysteine residues; this process can be reversed by oxidation of kera-
tin. Temporary reduction of hair by thioglycol and subsequent oxidation by
the oxygen of the air are principles underlying the cosmetic production of
permanent waves. The length of keratin fibers depends on their water con-
tent; thus when α-keratin is treated with water, the stretched /3-keratin is
formed. A pleated-sheet structure for /3-keratin has been put forward by
Pauling and Corey.
Stretching of wool forms parallel peptide chains which are linked to
each other by numerous hydrogen bonds. Wool shrinks on heating in water.
Since the — S — S — cross-links are not cleaved by heating, this reaction is
attributed to the cleavage of other interchain bonds.
Protein biosynthesis is at present a central interest of biochemists and
biophysicists.
B. Isolation of Lysozyme from Albumen

1. Introduction
Lysozyme is one of the smallest proteins. It has the ability to break down
(lyse) the cells of certain bacteria, whence its name.
Lysozyme has been obtained from albumen as the insoluble flavianate
by procedures involving solvent fractionation and precipitation (1,2). More
recently it was isolated by adsorption on bentonite and elution with 5%
pyridine solution adjusted to pH 5.3 (3), by direct crystallization at pH
9.0-9.5 (4), by use of an ion-exchange resin (5), and by chromatography on
hydroxyapatite (calcium phosphate adsorbent) (6).
Lysozyme has a molecular weight of approximately 17,500 and is a basic
protein with an isoelectric point of 10.5 to 11.0. It is regarded as an antibiotic
since it is able to kill microorganisms and even to dissolve living bacterial
bodies. Lysozyme is found in various animal species and is also produced by
bacteria, e.g., Bacillus subtilis and Staphylococcus aureus.
2. Principle
In the following procedure ( 7 ) , lysozyme is adsorbed on bentonite together
with other albumen globulins. The contaminating proteins are removed from
V. Proteins 325
the bentonite by washing successively with alkaline phosphate and 5 % aque-

ous pyridine. The lysozyme is then eluted from the bentonite with 5 % aque-
ous pyridine adjusted to pH 0.5 with sulfuric acid. The eluate is dialyzed.
Amorphous lysozyme is obtained by lyophilization of the solution.
3. Apparatus
Centrifuge
Blender
4. Materials
Bentonite Pyridine
Eggs Sodium chloride
Phosphate buffer (pH 7.5) Sodium hydrogen carbonate
Potassium chloride
5. Time
Adsorption and elution: 2 - 3 hours
Dialysis: 24 hours
6. Procedure
To 300 ml homogenized albumen (one dozen eggs of average size) are added
50 ml 10% bentonite suspension in 1% potassium chloride. The mixture is
stirred vigorously for 3 to 5 minutes until a smooth suspension is obtained.
The clay is separated by centrifugation and washed twice with 100-ml portions
of 0.5 M phosphate buffer (pH 7.5) and three times with 150-ml portions of
5% aqueous pyridine. The clay is separated by centrifugation after each
washing, and the supernatants, containing inactive proteins, are discarded.
Lysozyme is eluted by washing the clay twice with 100-ml portions of 5 %
aqueous pyridine solution, which has been adjusted to pH 5 with sulfuric acid.
The eluates are dialyzed against running tap water until no odor of pyridine
remains. The volume increases considerably during the dialysis, which lasts
for 24 hours. The pH of the final solution is approximately 6. Amorphous, but
essentially pure lysozyme is obtained by lyophillization of the solution. The
yield is 0 . 7 - 0 . 8 g. Crystalline lysozyme or its salts are obtained from the
amorphous material by one of the following procedures:
1. To 10 ml 5 % solution of amorphous lysozyme is added 0.5 g sodium
hydrogen carbonate (final pH 8 . 0 - 8 . 5 ) , and the solution is allowed to
stand at room temperature until lysozyme carbonate crystallizes.
2. To 10 ml 5 % solution of amorphous lysozyme is added 0.5 g sodium
chloride, and the pH is adjusted to 9.5 to 10.0 with sodium hydroxide.
The solution is stored at 4°C. Crystalline isoelectric lysozyme

separates.
3. A 5 % solution of amorphous lysozyme is adjusted to pH 4.5 with
hydrochloric acid, and 5% solid sodium chloride is added. The solution
is stored at 4°C, and crystalline lysozyme chloride is deposited within 4
to 5 days.
4. A 2% solution of isoelectric lysozyme in hydrobromic acid is adjusted
to pH 6.0, and 5 % solid potassium bromide is added. On standing at
room temperature, the solution deposits crystals of lysozyme bromide.
a. IR Spectrum of lysozyme
- 1
3440 c m : hydroxylamino groups
3076: aromatic C—H vibration of the tyrosine group or overtone of the
amide II band
1652: C = 0 stretching of —CO—NH—
1527: amide I I , Ν—Η deformation
1438, 1390: methylene and methyl bending
1290, 1242: C—Ν stretching in secondary amides
1098: aliphatic hydroxy amino acid
References
1. Wolff, L. K. (1927). Z. Immunitatforsch. 50, 88.
2. Meyer, K . , Thompson, R . , Palmer, J . , and Korazo, D . (1936). J. Biol. Chem. 113, 303.
3. Alderton, G . , Ward, W. H., and Fevold, H. L. (1945). / . Biol. Chem. 157, 43.
4. Alderton, G . , and Fevold, H. L. (1946). J. Biol. Chem. 164, 1.
5. Tallan, Η. H., and Stein, W. H. (1953). / . Biol. Chem. 200, 507.
6. Tiselius, Α . , Hjerten, S., and Levin, O. (1956). Arch. Biochem. Biophys. 65, 132.
7. Fevold, H. L . , and Alderton, G. (1949). Biochem. Prepns. 1, 67.
Recommended Review
1. Fevold, H. L. (1951). Egg proteins. In "Advances in Protein Chemistry(M. L. Anson,
J . T. Edsall, and K. Bailey, eds.), Vol. 6, p. 187. Academic Press, New York.
C. Isolation and Separation of Proteins of Groundnuts

1. Introduction
The proteins of groundnuts were first investigated by Ritthausen in 1880. He
extracted the proteins from the oil-free groundnut meal with aqueous sodium
chloride and weakly basic solutions, and precipitated them by acidification.
He considered the solids he obtained to be a homogeneous compound. The
investigations of Johns and Jones (1) have indicated that the total protein of
groundnuts consists of globulins and a very small amount of heat-coagulable
albumin. By means of ammonium sulfate fractionation they separated the
V. Proteins 327
globulins into two fractions, arachin and conarachin. Later, Jones and Horn
(2) stated that arachin could be prepared from 1 0 % sodium chloride extract
by dilution until the extract became cloudy, followed by saturation with C 0 2
or by addition of two volumes of saturated ammonium sulfate to three
volumes of the extract. Conarachin could be isolated by complete saturation
with ammonium sulfate.
Irving, Fontaine, and Warner (3) carried out electrophoretic analyses of
groundnut meal and concluded that it contained at least three, and probably
four, components. Similar observations were made by Karon, Adams, and
Altschul (4).
2. Principle
The method described below is based on (5).
3. Apparatus
4. Materials
Groundnuts Sodium hyroxide
Petroleum ether Sulfuric acid
Sodium chloride
5. Time
2 - 3 hours
6. Procedure
a. Isolation of arachin and conarachin
Fifty g blanched groundnuts and 200 ml light petroleum are refluxed for 1 hr
and filtered in order to expel the oil. The solid residue is dried in air and then
extracted with 0 . 1 % sodium hydroxide solution. The solution of sodium
proteinate is filtered off, and the protein is precipitated by addition of acid or
S 0 2 until the isoelectric range (around 5) is reached. The protein is allowed to
settle, filtered and washed free from salt and is then dried.
Arachin and conarachin can be prepared by two alternative methods.
1. Dried protein (4 g) is shaken with 100 ml 2 % aqueous sodium chloride
to give a solution of conarachin. The residue is extracted with 100 ml
10% aqueous sodium chloride to give a solution of arachin and an
insoluble residue.
2. Protein (4 g) is extracted with 100 ml 1 0 % aqueous sodium chloride to
give a solution of arachin and conarachin, and an insoluble solid. The
solution is diluted with four times its volume of water in order to
precipitate arachin; conarachin remains in solution. Conarachin may be
precipitated from the aqueous solution by heating.
b. Paper chromatography
The round-paper chromatographic technique is used for the separation and
identification of arachin and conarachin: one drop of a solution of groundnut
protein in 1 0 % aqueous sodium chloride is placed in the center of the paper.
Aqueous sodium chloride, 1 0 % , serving as the developing solvent, is placed
in an uncovered petri dish. Thus, the water from the paper Chromatograph
evaporates and the salt solution spreads upward. After about 15 min, the
chromatography is complete. The paper is dried and immersed in a 0.05%
solution of Solway purple containing 0 . 5 % sulfuric acid in a photographic
developing dish at a temperature of 50 to 90°C. After rocking the dish for
5 min, the dye solution is poured off, and the paper is washed in several
changes of warm water and finally dried. The proteins show up as violet-
colored patches on the chromatograms. The front line is identified as con-
arachin, and the rear line as arachin.
References
1. Johns, C. O., and Jones, D . B . (1916). / . Biol. Chem. 28, 77.
2. Jones, D . B . , and Horn, M. J . (1930). J. Agric. Res. 40, 672.
3. Irving, G. W., Fontaine, T. D . , and Warner, R . C. (1945). Arch. Biochem. 7, 475.
4. Karon, M. L . , Adams, M. E . , and Altschul, A. M. (1950). / . Phys. Colloid Chem. 54, 56.
5. Thomson, R . H. K. (1952). Biochem. J. 5 1 , 118.
Recommended Reviews
1. Pace, J . (1955). Seed proteins. In "Modern Methods of Plant Analysis." (K. Paech,
and M. V . Tracey, eds.), Vol. 4, p. 69. Springer-Verlag, New York.
2. Natarajan, K. R . (1980). Peanut protein ingredients: Preparation, properties, and food uses.
1
In "Advances in Food Research, ' Vol. 26, p. 216. Academic Press, New York.
D. Thin-Layer Chromatography of Proteins

1. Introduction
The determination of the molecular weights of proteins by means of gel
filtration on cross-linked dextran gels (Sephadex) has been described by a
number of authors. Whitaker (1) has covered the molecular weight range
13,000-40,200 using Sephadex G-75, and the range 13,000-76,000 using
Sephadex G-100. Wieland, Duesberg, and Determann (2) have used
Sephadex G-200 for proteins of molecular weight 13,000-150,000.
The advantages of thin-layer chromatography—speed and adaptability
to very small samples—make it very attractive for the fractionation of pro-
teins on the ultramicro scale. The availability of the loosely cross-linked
beadform materials—Sephadex G-100 and G-200—has extended the upper
molecular weight limit for the successful chromatography of proteins to at
least 180,000 (3).
V. Proteins 329
2. Principle
The procedure outlined below is according to (3).
3. Apparatus
Glass plates
Plastic box
Thin-layer applicator
4. Materials
Naphthalene Black 12B Sephadex G-100 and G-200
Nigrosin Sodium chloride
Proteins (see procedure) Sodium phosphate
6. Procedure
Sephadex gel powder (G-100) is distended in a suitable buffer for an appropri-
ate time. Each gram of Sephadex G-100, together with 19 ml buffer solu-
tion (0.02 M sodium phosphate containing 0.2 M sodium chloride), is allowed
to swell for 24 hr at pH 7. For each gram of G-200, 25 ml buffer is added and
left for 24 to 48 hr. The gel is then spread over glass plates to a thickness
of 0.5 mm with an applicator. Glass plates of dimensions 20 x 30 and
20 x 40 cm are commonly used. The coated plates are placed in a flat plastic
box and leant against a buffer reservoir, which is placed on a small table of
adjustable height for ready variation of the inclination of the plate. A sheet of
thick filter paper (Whatman 3 MM) is applied to the upper end of the plate
via a slit in the box. It ensures contact between the gel layer and the buffer,
providing for a flow of liquid through the gel. It is advisable to let the liquid
flow through the plates for at least 1 hr before the run. The samples are then
applied with capillary pipettes as round spots 2 - 4 mm in diameter, corres-
ponding to sample volumes of about 1-5 ul.
a. Development
Development is performed with the above-mentioned buffer solution ( 4 -
15 hr).
b. Detection
Upon completion of the chromatographic run, a damp sheet of Whatman
No. 1 paper is deposited on the Sephadex layer so as to achieve perfect ad-
herence between paper and gel. Under these conditions some of the chroma-
tographed material passes from the Sephadex gel to the paper. After 30 to 40
min, the paper is carefully removed from the layer, dried, and sprayed with
1% Naphthalene Black 12B in methanol-water-glacial acetic acid, 5 0 : 4 0 : 1 0 .
c. Recovery
The gel corresponding to the zones of the layer that, according to the
detecting paper, contain the separated substances, is removed from the plate
with a spatula, placed in a small centrifuge tube, and suspended in 5 ml water
or some other suitable solvent. The test tubes are then centrifuged. Most of
the analyzed substance is located in the supernatant. The proteins in the
following table can be separated by this technique.
Proteins Separated by TLC
3
Protein Molecular Weight x 1 0 "
Cytochrome C 13.0
Ribonuclease 13.6
Lysozyme 14.5
Myoglobin 16.9
a-Chymotrypsin 22.5
Trypsin 23.8
Ovomucoid 27.0
Pepsin 35.0
Ovalbumin 45.0
Hemoglobin 68.0
Bovin serum albumin 165.0
Bovin γ-globulin 180.0
Thyroglobulin 650.0
Macroglobulins 1000.0
References
1. Whitaker, J . R . (1963). Anal. Chem. 35, 1950.
2. Weiland, T . , Duesberg, P., and Determann, H. (1963). Biochem. Z. 337, 303.
3. Morris, C. J . O. R . (1964). J. Chromatogr. 16, 167.
Recommended Review
1. Fasella, P., Giartosio, Α . , and Turano, C. (1964). Applications of TLC on Sephadex to the
study of proteins. In "Thin-layer Chromatography" (G. B . Marini Bettolo, ed.), p. 205.
Elsevier, New York.
E. Questions
1. Dehne and describe a gene, a virus, and an enzyme.

2. Define the following terms: a. conjugated protein; b. derived protein;
c. prosthetic group.
3. Distinguish between fibrous and globular proteins with regard to
composition, structure, sources, and physical characteristics.
VI. Pteridines 331
4. Give the name and the source of a. three proteins that are enzymes;
b. one protein that is a hormone.
5. Which linkage is responsible for the crosss-linking of protein chains?
Which is responsible for the helical conformation?
6. What is Edman degradation?
7. Describe three methods for determining the molecular weight of
proteins.
8. Name some industrial uses of proteins.
9. What is the relationship between DNA, RNA, and protein
biosynthesis?
F. Recommended Books
1. Bailey, J . L. (1962). "Techniques in Protein Chemistry." Elsevier,

New York.
2. Fox, S. W., and Foster, J . F. (1957). "Introduction to Protein
Chemistry." John Wiley, New York.
3. Harris, R . J . C. (ed.) (1961). "Protein Biosynthesis." Academic
Press, New York.
4. Haurowitz, F. (1963). "The Chemistry and Function of Proteins"
5. Neurath, H., and Baily, K. (eds.) (1954). "The Proteins." Academic
Press, New York.
6. Ramachandran, G. N. (ed.) (1963). "Aspects of Protein Structure"
7. Scopes, R . K. (1987). "Protein Purification: Principles and Practice"
8. Springall, H. D. (1954). "The Structural Chemistry of
Proteins."Academic Press, New York.
9. Watson, J . D. (1965). "Molecular Biology of the Gene." Benjamin,
New York.
10. Wiseman, A. (1965). "Organization for Protein Biosynthesis."
Blackwell Scientific Publications, Oxford, England.
VI. PTERIDINES
A. Introduction
Pteridines are the pigments found in the wings of insects and in the eyes and
skin of fish, amphibia, and reptiles. The pteridine system is a combination of a
pyrazine ring and a pyrimidine ring.
Many of the naturally occurring pteridines have a 2-amino group and a

4-hydroxy group.
Xanthopterin, isoxanthopterin, leucopterin, and erythropterin are the
butterfly wing pigments; xanthopterin is also found in wasp wings, and in
human urine, liver, kidneys, spleen, and pancreas.
Xanthopterin
Isoxanthopterin Leucopterin
HO OH
Erythropterin
Pterorhodin has been found in butterfly wings and in the eyes of Ephestia and
Ptychopoda.
Η Η
HN NH
Η 2 Ν ^ Ν ^ Ν ^ € ^ Ν ^ Ν ^ Ν Η 2
Η Η Η
Pterorhodin
The yellow pteridines (sepiapterin and isosepiapterin) and three red

pigments (drosopterin, isodrosopterin, and neodrosopterin) have been iso-
lated from the fruit fly Drosophila melanogaster.
A widely occurring natural pterin is biopterin, which has been isolated
from human urine, from the fruit fly, from the Mediterranean flour moth, and
from the royal jelly of bees.
VI. Pteridines 333
r» H H
I ï J O H OH
Biopterin
Folic acid, a vitamin, has a pteridine moiety in its molecule.
OH
^ ^ j f ^ ^ COOH
H2N^N^N^CH2NH-Y VcONHÇH
CH2
I
CH2
COOH
Folic acid
The two methods for the synthesis of pteridines start either from the
pyrazine or the pyrimidine half of the pteridine molecule.
1. Synthesis from Pyrimidines

Since pyrimidines are relatively readily accessible, the Isay reaction, i.e., the
condensation of a 4,5-diaminopyrimidine with a 1,2-dicarbonyl compound,
continues to be of major importance:
H r v +. c=o
N H z
O ^ N ^ : N H 2 < r °
H R
4-Amino-5-nitrosopyrimidines can be condensed not only with ketones and

aldehydes, but also with nitriles and esters that have an activated methylene
group adjacent to the functional group.
Ν Ο
Η Ν ^ γ C 6H 5C O C H 2C H 3> Η Ν ^ γ ^ ^ γ ^
H 2 N ^ N ^ N H 2 H 2 N ^ N ^ N ^ C 6 H 5
2. Synthesis from Pyrazines

Pteridine syntheses based on pyrazine derivatives have been carried out only
rarely because such derivatives are not readily accessible.
N-\ . C O N H 2
H C O O H
Ν NH2
Since the majority of pteridines are insoluble in most solvents and
possess very high melting points, the most reliable physical properties reflect-
ing homogeneity are the Rf values (obtained by paper or thin-layer chroma-
tography) and ultraviolet spectra.
Recent chemical and microbiological research has indicated that the
pteridine ring arises from a purine nucleus.
B. Isolation of Pteridines from the Fruit Fly, Drosophila

melanogaster
1. Introduction
The yellow to red pterins from the fruit fly Drosophila melanogaster consti-
tute an important group of natural pteridine derivatives.
OH Ο
II
Η
I
c -C-— C H ,
I
Η Η
OH
H 2N
Sepiapterin
OH OH OH ο
I II
: - C H 2- C H 3 N ^ X - C H 2- C H 3
Η
H 2N H,N
Η
Isosepiapterin
CH, "C — C H 3
OH OH
H,N
Drosopterin
VI. Pteridines 335
Viscontini and his coworkers ( 1 , 2 ) have shown by means of chroma-

tography that the Drosophila pterins consist of the yellow compounds,
sepiapterin and isosepiapterin, as well as the orange to red compounds,
drosopterin, isodrosopterin, and neodrosopterin. Sepiapterin was isolated in
the form of yellow crystals from D. melanogaster, the sepia mutant of which
accumulates large concentrations of this pigment (3). It is also found in
amphibian skin ( 4 ) , in fish (5), and in the epidermis of the lern mutant of the
silk moth Bombyx mon (6).
ÇH3
H-C-OH
OH !
H 2N
Isodrosopterin
Isosepiapterin was isolated in crystalline form for the first time from
the sepia mutant of Drosophila (1). Larger concentrations of isosepiapterin
were found in the blue-green alga Anacystis nidulans (7). Viscontini (2) was
the first to separate the water-soluble, red eye-pigments of Drosophila into
drosopterin, isodrosopterin, and neodrosopterin. These pigments also occur
in the skin of some fish (8) and amphibia ( 9 ) , as well as in the skin folds of
various reptiles (10).
2. Principle
The procedure outlined below is based on (1) and (2).
3. Apparatus
Chromatographic column
Blender
4. Materials
Acetic acid Methanol
Ammonium acetate Propanol
Ammonium chloride Pyridine
Ammodium hydroxide Sepia flies (can be prepared according to
Butanol Demerec, M., The Biology of Drosophila,
Cellulose powder John Wiley, New York, 1950).
Ethyl acetate
5. Time
4 - 5 hours
6. Procedure
a. Isolation of the yellow pigments
Sepia flies (200 g) are macerated in a blender in 500 ml ethanol and 200 g
cellulose powder. The suspension is packed into a chromatographic column
(10 x 12 cm) on top of cellulose powder, and elution is immediately com-
menced with propanol-1% aqueous ammonium acetate, 1:1. The yellow
pigment is washed from the column, and the eluates are evaporated to 30
to 50 ml under reduced pressure. This solution is applied to a column
(10 x 60 cm) of cellulose packed in the same solvent. A blue pigment is eluted
first, followed by a yellow zone which is eluted with butanol-acetic acid-
water, 2 0 : 3 : 3 , and contains isosepiapterin, sepiapterin, and riboflavin.
The yellow solution should be immediately neutralized to prevent de-
com-position of the pigments. It is then rechromatographed on a cellulose-
packed column, eluting with water. The eluates are concentrated almost to
dryness, leaving long, yellow needles. Paper chromatography is carried out
with four solvents:
1. Butanol-acetic acid-water, 2 0 : 3 : 3 .
2. Propanol-1% ammonium hydroxide, 2 : 1 .
3. Ammonium chloride, 1% aqueous.
4. Propanol-2% ammonium acetate, 1:1.
Retention Characteristics of Yellow Pigments
*/ in Solvent
Pteridine 1 2 3 4
Sepiapterin 0.22 0.42 0.33 0.60

Isosepiapterin 0.43 0.52 0.25 0.65
b. Isolation of red pigments

Cellulose powder (400 g) and 400 g blenderized flies are thoroughly mixed
with 50 ml 8 0 % methanol. The slurry is packed into a chromatographic
column (18 x 20 cm) containing 100 g cellulose powder and is eluted with
80% methanol until the red pigments are adsorbed on the upper part of the
column. Elution is continued with 0 . 1 % aqueous ammonium acetate solution
until three distinct zones are formed; these are then eluted separately. Each
VI. Pteridines 337
eluate is concentrated to about 100 ml in vacuo and rechromatographed on

9 x 25 cm columns packed with cellulose, eluting first with distilled water to
remove impurities. The pigments are rapidly eluted with 0 . 5 % aqueous
ammonium hydroxide. The solutions are concentrated under reduced pres-
sure until turbidity, three volumes ethanol and four volumes ether are added;
the mixture is left in the cold for 24 hr. The yields are 2 mg isodrosopterin,
15 mg drosopterin, and 2 mg neodrosopterin. Paper chromatography is car-
ried out with four solvents:
1. Butanol-acetic acid-water, 2 0 : 3 : 7 .
2. Propanol-1% ammonium hydroxide, 2 : 1 .
3. Pyridine-ethyl acetate-water, 4 : 4 : 3 .
4. Propanol-2% aqueous ammonium acetate, 1:1.
Retention Characteristics of Red Pigments
in Solvent
Pteridine 1 2 3 4
Neodrosopterin 0.05 0.07 0.04 0.11

Drosopterin 0.10 0.14 0.10 0.19
Isodrosopterin 0.11 0.14 0.10 0.25
References
1. Viscontini, M . , and Mohlamann, E . , (1959). Helv. Chim. Acta 42, 836.
2. Viscontini, M . , Hadorn, E . and Karrer, P. (1957). Helv. Chim. Acta 4 0 , 579.
3. Forrest, H. S., and Mitchell, H. K . (1958). J. Am. Chem. Soc. 76, 5656.
4. Hama, T . , and Obika, M. (1960). Nature 187, 326.
5. Hama, T . , Matsumoto, J . , and Mori, Y . (1960). Proc. Imp. Acad. (Tokyo) 36, 346.
6. Nawa, S., and Taira, T. (1954). Proc. Imp. Acad. (Tokyo) 30, 632.
7. Forrest, H. S., van Baalen, C , and Myers, J . (1959). Arch. Biochem. Biophys. 83, 508.
8. Kaufmann, T . (1959). Z. Naturforsch 14b, 358.
9. Hama, T . , (1963). "Third Intern. Symp. on Pteridines." Stuttgart, 1962. Pergamon Press,
London, England.
10. Ortiz, E . , Throckmorton, L . H., and Williams-Ashman, G. H. (1962). Nature 196, 596.
Recommended Reviews
1. Forrest, H. S. (1962). Pteridines, structure and metabolism. In "Comparative Biochemis-
try," ( M . Florkin, and H. S. Mason, eds.), Vol. 4, p. 615. Academic Press, New York.
2. Viscontini, M. (1964). The structure of sepiapterin and drosopterin. In "Pteridine Chemis-
try," (W. Pfleiderer, and E . C. Taylor, eds.), Proceedings of the Third International
Symposium, Stuttgart, 1962. Pergamon Press, London, England.
C. Synthesis of Pteridines
1. Introduction
Pteridines can be synthesized by two main pathways, namely, fusion of a
pyrimidine ring onto a pyrazine derivative, or fusion of a pyrazine ring onto a
pyrimidine derivative.
Since pyrimidines are relatively readily accessible (1), the Isay reaction,
i.e., condensation of a 4,5-diaminopyrimidine with a 1,2-dicarbonyl com-
pound, continues to be of major importance (2). The dicarbonyl compounds
that have been used include a dialdehyde (glyoxal), aldehydo-ketones
(phenylglyoxal), diketones (diacetyl ( 3 ) , benzil ( 4 ) , 13 higher homologs of
dipropionyl ( 5 ) , an aldehydo acid (glyoxylic acid) (6), and keto acids such as
pyruvic acid (7) and dibasic acid (8). The Isay reaction can be carried out
under neutral, acid, and alkaline conditions; neutral condensation usually
gives the best yields. When the dicarbonyl compound in Isay's reaction is not
symmetrical, two isomers can arise (9).
OH
NH
H 2N - C - N H 2H C 1 + CNCH2COOC2H5
Guanidine hydrochloride Ethyl cyanoacetate
2,6-Di amino-4-hydroxy pyri midine
4- Hydroxy-2,5,6-triamino pyri midine
OH OH
2-Amino-4-hydroxy-6,7-dimethyl pteridine 2-Amino-4-hydroxy pteridine

VI. Pteridines 339
2. Principle
The following procedure (10) involves the use of 4-hydroxy-2,5,6-triamino-
pyridine, prepared by condensation of guanidine and ethyl cyanoacetate to
form the 2,6-diamino-4-hydroxypyrimidine, which is nitrosated to the 5-
nitroso derivative. The nitroso group is reduced by sodium hydrosulfite to the
desired substituted pyrimidine. The latter is converted into 2-amino-4-
hydroxy-6,7-dimethylpteridine by treatment with biacetyl; the reaction with
glyoxal leads to the formation of 2-amino-4-hyroxypteridine.
3. Apparatus
4. Materials
Biacetyl Hydrochloric acid
Ethanol, absolute Sodium, metal
Ethyl cyanoacetate Sodium bisulfite
Formic acid Sodium hydrosulfite
Glyoxal Sodium hydroxide
Guanidine hydrochloride Sodium nitrite
5. Time
5 - 6 hours
6. Procedure
a. 4-Hydroxy-2,5,6-triaminopyrimidine bisulfite
To a solution of sodium ethoxide, prepared by dissolving 3.5 g sodium in
150 ml absolute ethanol, are added 10 g guanidine hydrochloride and 13.5 g
ethyl cyanoacetate. The mixture is refluxed for 3 hr. Dilution with 100 ml
water and acidification with 10 ml concentrated hydrochloric acid liberate
2,6-diamino-4-hydroxypyrimidine, which is nitrosated by slow addition, with
stirring, of 10 g sodium nitrite dissolved in 30 ml water. After heating to
boiling, the mixture is allowed to cool. The crystalline, bright rose 5-nitroso
derivative is filtered and washed well with water. The material is then sus-
pended in 150 ml water and, after addition of 8 ml 2 0 % sodium hydroxide, is
heated to 70 to 80°C. Reduction of the nitroso group is effected by the
addition of 50 g sodium hydrosulfite over a period of 15 min, with vigorous
stirring. Heating and stirring are continued for 30 min, during which period
the color is almost completely discharged. The solution is then heated to the
boiling point and filtered through a Büchner funnel. The light yellow prod-
uct crystallizes immediately. It is filtered and washed with cold water; yield,
20 g. The product may be crystallized from two parts of water.
b. 2-Amino-4-hydroxypteridine
A solution of 15 g glyoxal sodium bisulfite in 50 ml hot water is added, with
stirring, to a solution of 10 g 4-hydroxy-2,5,6-triaminopyrimidine bisulfite in
50 ml hot water. The resulting clear, yellow solution soon begins to deposit a
light yellow solid, which is heated for 2 hr on a steam bath. After cooling, the
solid is collected by filtration, washed with water, and dried. The yield is 4 g.
The compound is recrystallized as yellow microcrystals by dissolving it in
boiling formic acid and adding water to incipient precipitation.
c. UV spectrum of 2-amino-4-hydroxypteridine
A o,uvNaOH 2 5 5 μπ ι( l eo g4 2 0; ) 3 85 (3 8 ) 2
Pteridine is a naphthalenoid, but differs from naphthalene in that it possesses

some unshared electrons, namely those located on the nitrogen atoms of the
nucleus. (Naphthalene main absorptions in ethanol are 275 τημ (log ε 3.93)
and 310 (2.56)). 2-Amino-4-hydroxypteridine has an acidic hydroxyl group
(like that of phenol) and an amino group, so that the actual constitution of the
molecule depends on the pH of the medium. In alkali, the structure of the
compound is that of the anion:
cr
d. 2-Amino-4-hydroxy-6,7-dimethylpteridine
To a solution of 10 g 4-hydroxy-2,5,6-triaminopyrimidine bisulfite in 50 ml
hot water is added 10 g biacetyl. The condensation product begins to separate
immediately. In order to complete the reaction, the mixture is heated on the
steam bath for 2 hr. After cooling, the solid material is collected by filtration
and washed with water and then with 9 5 % ethanol; yield, 6 g. Recrystalliza-
tion from 0.5N hydrochloric acid gives yellow microcrystalline rods.
e. UV spectrum of 2-amino-4-hydroxy-6,7-dimethylpteridine
NaOH
^°max 250m/i (loge 4.34); 355 (3.94)
Note that the methyl substitution has practically no effect on the absorption.
References
1. Brown, D . J . (1952). J. Appl. Chem. 2, 239.
2. Isay, O. (1906). Ber. 3 9 , 250.
3. Kuhn, R . , and Cook, A . H. (1937). Ber. 7 0 , 761.
4. Cain, C. K . , Taylor, E . C , and Daniel, L. J . (1949). / . Am. Chem. Soc. 7 1 , 892.
VI. Pteridines 341
5. Campbell, N. R . , Dunsmuir, J . H., and Fitzgerald, Μ. Ε . H. (1950). J. Chem. Soc. 2743.

6. Koschara, W. (1943). Z. Physiol. Chem. 277, 159.
7. Elion, G . , and Hitchings, G . H. / . Am. Chem. Soc. 69, 2553.
8. Forrest, H. S., Hull, R . , Rodda, H. J . , and Todd, A . R . (1951). J. Chem. Soc. 3.
9. Elion, G . , Hitchings, G . H., and Rüssel, P. B. (1950). / . Am. Chem. Soc. 72, 78.
10. Cain, C. K . , Mallete, M. F . , and Taylor, E . C. (1946). / . Am. Chem. Soc. 68, 1998.
Recommended Reviews
1. Albert, A . (1952). The pteridines. Quart. Revs. 6, 197.
2. Elderfield, R . C , and Mehta, A . C. (1967). The pteridines. In "Heterocyclic Compounds,"
( R . C. Elderfield, ed.), Vol. 9, p. 1. John Wiley, New York.
3. Pfleiderer, W. (1964). Recent developments in the chemistry of pteridines. Angew. Chem.
Intern. Edit. 3, 114.
D. Thin-Layer Chromatography of Pteridines

1. Introduction
Paper chromatography has been extensively applied to naturally occurring
pteridines. Systematic investigations of the suitability of various solvents for
the separation of natural pteridines have been carried out by Tschesche and
Korte (1) with the silkworm Bombyx mon, by Blair and Graham (2) with
green snakes, by Forrest and Mitchell (3) and Viscontini, Hadorn, and Karrer
(4) with fruit flies, by Schmidt and Viscontini (5) with red ants, by Viscontini,
Kuhn, and Egelhaaf (6) with the flour moth.
Recently, thin-layer chromatography was used for the separation and
identification of pteridines. Nicolaus (7) used silica gel G, while Merlini and
Nasini (8) and Ikan and Ishay (9) used cellulose M N - 3 0 0 G . This technique
has the following advantages over paper chromatography: smaller amounts
may be used, the spots appear smaller, and a better separation can be
achieved in a shorter time.
Pteridines may be detected on the chromatoplates by observing their
fluorescence under ultraviolet light (254 πιμ).
2. Principle
The procedure outlined below is according to (7).
3. Materials
Ammonium hydroxide Dimethylformamide
Cellulose powder, M N - 3 0 0 G Pteridines (see Table 10)
Citric acid Silica gel G
4. Procedure
a. Plates
Silica gel G plates, 0.25 mm thick, 20 x 20 cm, are used.
b. Development
The samples of pteridines are applied as a 1% solution in dilute ammonium
hydroxide.
Development is accomplished in four solvent systems (Table 10):
1. dimethylformamide-water, 19:1
2. citric acid, aqueous, 5 %
3. ammonium hydroxide, 1 0 %
4. ammonium hydroxide, 2 5 %
c. Detection
The spots on the chromatogram may be detected by observation under ul-
traviolet light, at 254 and 360 χημ.
Development of Pteridines
Rf in Solvent System
Pteridine 1 2 3 4
2-Amino-4-hydroxy 0.55 0.78 0.95

2-Amino-6,7-dimethyl-4-hydroxy 0.65 0.46 0.91
2-Amino-4-hydroxy-6-methyl 0.65 0.69 0.93 0.92
2-Amino-4-hydroxy-7-methyl 0.88 0.60 0.92
2,4-Dihydroxy 0.00 0.88 0.92
6-Methylisoxanthopterin 0.88
7-Methylxanthopterin 0.88
Isoxanthopterin 0.80
2,4-Dihydroxy (lumazin) 0.83
d. Cellulose plates
The suspension for five plates (20 x 20 cm) is prepared by shaking 15 g
cellulose M N - 3 0 0 G with 90 ml distilled water for 30 sec; it is applied to a
thickness of 0.5 mm with an applicator. After 30 min at room temperature,
the plates are heated at 105°C for 30 min. Development may be accomplished
with n-propanol-1% ammonia, 2 : 1 .
References
1. Tschesche, R . , and Korte, F . (1954). Ber. 87, 1713.
2. Blair, J . Α . , and Graham, J . (1955). Chem. Ind. (London) 1158.
3. Forrest, H. S., and Mitchell, Η. K . (1955). / . Am. Chem. Soc. 77, 4865.
VII. Pyrazines 343
4. Viscontini, M., Hadorn, E . , and Karrer, P. (1957). Helv. Chim. Acta 4 0 , 579.
5. Schmidt, G. H., and Viscontini, M. (1962). Helv. Chim. Acta 4 5 , 1571.
6. Viscontini, M . , Kuhn, Α . , and Egelhaaf, Α . (1956). Ζ. Naturforsch, lib, 501.
7. Nicolaus, B . J . R . (1960). J. Chromatogr. 4 , 384.
8. Merlini, L . , and Nasini, G . (1966). / . Insect Physiol. 12, 123.
9. Ikan, R . , and Ishay, J . (1967). J. Insect Physiol. 13, 159.
E. Questions
1. What are the main pteridines of bees and wasps?

2. How are pteridines isolated and identified?
3. Describe the occurrence, structure, and biological function of biopterin
and folic acid.
4. Explain the structural and biogenetic relationship between purines and
pteridines.
F. Recommended Books
1. Pfleiderer, W. (ed.) (1975). "Chemistry and Biology of Pteridines." W.

de Gruyter, New York.
2. Pfleiderer, W., and Taylor, E . C. (eds.) (1964). "Pteridine Chemistry."
Proceedings of the Third International Symposium, Stuttgart, 1962.
Pergamon Press, London.
3. Wolstenholme, G. E . W . , and Cameron, M. P. (eds.) (1954). "Ciba
Foundation Symposium on Chemistry and Biology of Pteridines."
Churchill, London.
VII. PYRAZINES
A. Introduction
Pyrazine is a six-membered ring built up of carbon and two atoms of nitrogen.
B. Isolation and Characterization of Pyrazines, the Volatile

Constituents of Bell Peppers
1. Introduction
Pyrazines are important sensory constituents of foods. More than 50 different
alkylpyrazines were detected in about 30 natural or manufactured, cooked,
roasted, or fermented products of vegetable or animal sources. Among the 43

pyrazines so far identified in cocoa, there are not fewer than 27 alkylpyr-
azines. 3-Ethyl-2,5-dimethyl pyrazine, for instance, is a contributor to the
odoriferous principle of cocoa aroma and one of the most potent odorants
derived from potato chips. It is curious to note that the chocolate-smelling
alarm pheromone of an American species Odontromachus (an ant species)
mainly consists of alkylpyrazines.
Among the pyrazines, the acetyl derivatives occupy a particular position
as flavoring agents. They have a surprisingly intense and characteristic
roasted note, which is reminiscent of popcorn. Acetylpyrazine was detected
(1) (2)
for the first time in 1969 in sesame o i l . It was also detected in popcorn ,
(3) (4) ( 5) (6)
roasted peanuts , t o b a c c o , roasted coffee and roasted almonds .
Odor thresholds of some pyrazines are summarized below:
12
Compound per 10 parts of water
2-Methoxy-3-hexylpyrazine 1
2-Methoxy-3-isobutyl pyrazine 2
2-Methoxy-3-propyl pyrazine 6
2-Methoxy-3-isopropyl pyrazine 2
2-Methoxy-3-ethyl pyrazine 400
2-Methoxy-3-methyl pyrazine 4,000
2-M ethoxy-py razine 700,000
2,5-Dimethyl pyrazine 1,800,000
Pyrazine 175,000,000
Green bell peppers are widely accepted for use both as food and as
flavoring for other foods. They differ from other members of the genus
Capsicum in that they generally do not have the hot taste associated with the
chili and the tabasco types. The hot taste has long been known to be due to
the presence of the essentially nonvolatile compound capsaicin (,/V-(4-
hydroxy-3-methoxy-benzyl)-8-methyl-non-ir«n5-6-enamide).
The odor threshold of 2-methoxy-3-isobutylpyrazine (the main odorous
12
principle of bell peppers) was found to be 2 parts per 1 0 parts of water.
Months after this compound was synthesized by Buttery and coworkers, his
end of the building smelled of freshly chopped green bell peppers.
2. Principle
Green bell peppers are crushed and steam distilled, and the oily product is
extracted with hexane.
The volatile constituents are characterized by G C / M S technique. The
GC fractions are collected, and their I R and NMR specta are measured. The
odorous potency can also be estimated by smelling.
VII. Pyrazines 345
3. Apparatus
Capillary column
G C / M S apparatus
I R spectrometer
4. Materials
Green bell peppers
Hexane
5. Time
3 hours
6. Procedure
The green bell peppers are cut open, the seeds are removed, and the peppers
are macerated in a blender. The resulting puree is steam distilled, and the
distillate is extracted with hexane. In a typical isolation, a 0.5 kg portion of
bell pepper puree yields 1 mg of an oil.
a. Capillary GLC mass spectral analysis

A 1000-foot x 0.03 inch i.d. stainless steel capillary column coated with sili-
cone S F 96-100 is used. The column is programmed from 70° to 170°C at
0.5°C/min. Nitrogen at a 20 psi inlet pressure is used as the carrier gas. The
effluent from the end of the column is split, about 1 0 % going to a flame
ionization detector and the rest, to a silicone rubber membrane molecular
separator of the Llewellyn type. The separator introduces components into
the mass spectrometer. The outlet from the molecular separator to the
atmosphere generally contains sufficient excess sample for informal sensory
odor detection and evaluation.
b. Separation of samples for infrared and proton magnetic resonance spectra

For measurements of I R spectra of major components, samples are separated
from the G L C column and collected in 150 x 1 mm borosilicate glass melting-
point tubes, which are then sealed at both ends and stored at - 2 0 ° C until the
spectra can be measured. Larger amounts of samples are isolated using a
10-foot x 1/4 inch o.d. silicone S F 9 5 - 3 5 0 packed G L C column and collecting
the samples in 150 x 3 mm borosilicate glass tubes.
The major G L C peaks are limonene, trans-ß-ocimene, 2-methoxy-3-
isobutyl-pyrazine, and methyl salicylate. The molecular ion of 2-methoxy-3-
isobutylpyrazine is 166.
Aroma significance of bell pepper components may be estimated by
smelling.
The table below summarizes the odor thresholds of some bell pepper consti-
tuents:
Odor Thresholds of Bell Pepper Constituents
Compound Threshold in ppb
Hexanal 4.5
Furfural 3000
Hex-irans-2-enal 17
Heptan-2-one 140
Hex-ds-2-enol 70
Hept-frYws-3-en-2-one 56
Benzaldehyde 350
2-Pentylfuran 6
Limonene 10
Non-l-en-4-one 0.4
Phenylacetaldehyde 4
Linalool 6
Nona-iraws-2-en-4-one 0.9
1 -Methoxy-3-isobutylpyrazine 0.002
Nona-trans,trans-2,5-dien-4-one 4
Methyl salicylate 40
Deca-trans ,trans-2,4-dienal 0.07
The volatile oil of chili peppers also contains 2-methoxy-isobutyl-

pyrazine in the same order of concentration as found in bell peppers.
C. Questions
1. Describe the formation pathways of alkyl and acylpyrazines.

2. What are the main pyrazines of coffee, tea, potato chips, popcorn,
and peanuts?
3. Describe the organoleptic and sensory properties of some pyrazines.
D. Recommended Books
1. Maga, J . Α., and Siger, C. E . (1975). Pyrazines in foods. In

"Fenarolis Handbook of Flavor Ingredients." (T. E . Furia and N.
Bellanca, eds.), Vol. 1, p. 47. C R C Press, Boca Raton, Florida.
2· Maga, J . A. (1982). Pyrazines in flavour. In "Food Flavours, Part A."
(I. D . Morton and A. J . Macleod, eds.), p. 283. Elsevier, Amsterdam,
The Netherlands.
Bibliography 347
3. Hurrell, Κ. F . (1982). Maillard reaction in flavour. In "Food

Flavours, Part A." (I. A . Morton and A. J . Macleod, eds.), p. 399.
References
1. Takel, Y . , Nakatani, Y . , Kobayashi, Α . , and Yamanishi, T . (1970). Chem. Abstr. 7 2 ,
35670 g.
2. Walradt, J . P., Lindsay, R . C , and Libbey, L. M. (1970). / . Agr. Food Chem. 1 8 , 926.
3. Walradt, J . P., Pittet, A . O., Kinlin, T . E . , Maralidhara, R . , and Sanderson, A . (1971).
/. Agr. Food Chem. 1 9 , 972.
4. Demole, E . , and Berthet, D . (1972). Helv. Chim. Acta. 5 5 , 1866.
5. Vitzthum, Ο. F . , and Werkhoff, P. (1974). Ζ. Lebensm. Unters, Forsch. 156, 300.
6. Takei, Y . , and Yamanashi, T . (1974). Agric. Biol. Chem. 3 8 , 2329.
7. Buttery, R . G . , Seifert, R . M., Gaudagni, D . G . , and Ling, L. C. (1969). / . Agr. Food
Chem. 17, 1322.
Recommended Reviews
1. Maga, J . A . (1982). Pyrazines in flavour. In "Food Flavours, Part Α . " (I. D . Morton and
A . J . Macleod, eds.), p. 283. Elsevier, Amsterdam, The Netherlands.
2. Ohloff, G . , and Flament, I. (1976). Recent developments in the field of naturally occurring
aroma components. Prog. Chem. Org. Nat. Prod. 3 5 , 431.
3. Ohloff, G . , and Flament, I. (1979). The role of heteroatomic substances in the aroma
compounds of foodstuffs. Prog. Chem. Org. Nat. Prod. 3 6 , 231.
BIBLIOGRAPHY
Recommended Books on Infrared Spectroscopy
Bellamy, L. J . (1958). "Infrared Spectra of Complex Molecules" Methuen, London, England.

Brame, E . G . and Grasselli, J . (1976). "Infrared and Raman Spectroscopy." Marcel Dekker,
New Y o r k .
Colthup, Ν. B . , Daly, L. H., and Wiberley, S. E . (1964). "Introduction to Infrared and Raman
Spectroscopy." Academic Press, New York.
Durig, J . R . , ed. (1990). "Applications of FT-1R Spectroscopy." Elsevier, New York.
Ferraro, J . R . , and Krishnan, K. (1989). "Practical Fourier Transform Infrared Spectroscopy."
Griffith, P. R . , and Haseth, J . A . (1986). "Fourier Transform Infrared Spectrometry." John
Wiley, New Y o r k .
Miller, R . G . J . ed. (1965). "Laboratory Methods in Infrared Spectroscopy " Heyden and Son,
London, England.
Nakanishi Koji (1962). "Infrared Absorption Spectroscopy." Holden Day, San Francisco and
Nankodo Company, Tokyo.
Pouchert, C. J . (1981). "The Aldrich Library of Infrared Spectra." Aldrich Chemical Co.
Milwaukee, Wisconsin.
Pouchert, C. J . (1989). "The Aldrich Library of FT-1R Spectra." Aldrich Chemical Co. Mil-
waukee, Wisconsin.
Rao, C. N. R . (1963). "Chemical Applications of Infrared Spectroscopy." Academic Press,
New York.
Smith, A. L. (1979). "Applied Infrared Spectroscopy." John Wiley, New York.

Szymanski, H. A . (1962). "Infrared Handbook." Plenum Press, New York.
Wilson, Ν. K., and Childers, J . W. (1989). Recent advances in the matrix isolation infrared
spectrometry of organic compounds. Applied Spectroscopy Reviews, 2 5 ( 1 ) , 1-61.
Recommended Books on Nuclear Magnetic Resonance Spectroscopy
Bovey, F . A. (1988). "Nuclear Magnetic Reasonance Spectroscopy." Academic Press, New

York.
Duddeck, H., and Dietrich, W. (1989). "Structure Elucidation by Modern NMR" Springer-
Verlag, New York.
Levy, G. C , Lichter, R . L . , and Nelsen, G. L. (1980). "Carbon-13 Nuclear Magnetic Resonance
Spectroscopy." John Wiley, New York.
Linskens, H. F . , and Jackson, J . E . (1988). "Nuclear Magnetic Resonance." Springer-Verlag,
New York.
Marshall, A. G . , and Verdun, F . R . (1989). "Fourier Transforms in NMR, Optical, and Mass
Spectrometry." Elsevier, Amsterdam, The Netherlands.
Mehring, M. (1983). "High Resolution NMR Spectroscopy of Solids." Springer-Verlag, New
York.
Pouchen, C. J . (1983). "The Aldrich Library of NMR Spectra." Aldrich Chemical Co., 1983.
Shaw, D . (1984). "Fourier Transform NMR Spectroscopy." Elsevier, Amsterdam, The Nether-
lands.
Wilson, M. A . (1987). "NMR Techniques and Applications in Geochemistry and Soil Chemistry."
Pergamon Press, London, England.
Recommended Books on Ultraviolet Spectroscopy
Gillam, A . E . , and Stern, E . S. (1957). "Introduction to Electronic Absorption Spectroscopy in

Organic Chemistry." Arnold, London, England.
Jaffe, H. H., and Orchin, M. (1962). "Theory and Applications of Ultraviolet Spectroscopy."
John Wiley, New York.
R a o , C. N. R . (1961). "Chemical Applications of Ultraviolet and Visible Spectroscopy." Butter-
worth, London, England.
Scott, A . I. (1964). "Interpretation of the Ultraviolet Spectra of Natural Products." Pergamon,
London, England.
(See also general texbooks on spectroscopy.)
General Textbooks on Spectroscopy
Baker, A. J . , and Cairns, T. (1965). "Spectroscopic Techniques in Organic Chemistry." Heyden

and Son, London, England.
Braude, Ε . Α . , and Nachod, F . C. (1955). "Determination of Organic Structures by Physical
Methods." Vol. 1. Academic Press, New York.
Brand, J . C. D . , and Eglinton, G. (1965). "Applications of Spectroscopy to Organic Chemistry."
Oldbourne Press, London, England.
Colthup, Ν. B . , Daly, L. H., and Wiberley, S. E . (1990). "Introduction to Infrared and Raman
Spectroscopy." Academic Press, New York.
Bibliography 349
Flett, M. St. C. (1962). "Physical Aids to the Organic Chemist." Elsevier, Amsterdam, The
Netherlands.
Fretsch, E . , Clere, T . , Seibl, J . , and Simon, W. eds. (1989). "Table of Spectral Data for Structure
Determination of Organic Compounds." Springer-Verlag, New York.
Pinder, A . R . (1965). "Physical Methods in Organic Chemistry." English Universities Press,
London, England.
Schwarz, J . C. P. (ed.) (1964). "Physical Methods in Organic Chemistry." Oliver and Boyd,
Edinburgh, Scotland.
Silverstein, R . M., and Bassler, G. C. (1963). "Spectrometry Identification of Organic Com-
pounds." John Wiley, New York.
Silverstein, R . M., Bassler, G. C , and Morrill, T. C. (1985). "Spectroscopic Identification of
Organic Compounds." John Wiley, New York.
Sixma, F . L. J . , and Wynberg, H. (1964). "A Manual of Physical Methods in Organic Chemis-
try." John Wiley, New Y o r k .
Recommended Books on Gas Chromatography
Burchfield, H. P., and Storrs, Ε . E . (1962). "Biochemical Applications of Gas Chromato-

graphy." Academic Press, New York.
Jennings, W. (1980). "Gas Chromatography with Glass Capillary Columns." Academic Press,
New York.
Ioffe, Β . V . , and Vitenberg, A . G. (1984). "Head-Space Analysis and Related Methods in Gas
Chromatography." John Wiley, New York.
Pery. J . A. (1981). "Introduction to Analytical Gas Chromatography." Marcel Dekker, New
York.
Verpoorte, R . , and Baerheim-Svendsen, A . (1984). "Chromatography of Alkaloids, Part B:
Gas-Liquid Chromatography and High-Performance Liquid Chromatography." Elsevier,
Recommended Books on Thin-Layer Chromatography
Baerheim-Svendsen, Α . , and Verpoorte, R . (1983). "Chromatography of Alkaloids, Part A:

Thin-Layer Chromatography." Elsevier, Amsterdam, The Netherlands.
Fried. B . , and Sherma, J . (1982). "Thin-Layer Chromatography." Marcel Dekker, New York.
Kirchner, J . G. (1978). "Thin-Layer Chromatography." John Wiley, New York.
Stahl, Ε . (1965). "Thin-Layer Chromatography." Academic Press, New York.
Touchstone, J . C., and Dobbins, M. F. (1978). "Practice of Thin-Layer Chromatography." John
Wiley, New York.
Wilson, I. D . , and Ruane, R . J . , ed. (1987). "Prospects for Chiral TLC" D . Stevenson and
I. D . Wilson , Pleum Press, p. 135. New York.
Zlatkes, Α . , and Kaiser, R . E . , ed. (1977). "HPTLC-High Performance Thin-Layer Chroma-
tography." Elsevier, Amsterdam, The Netherlands.
Reocmmended Books on Mass Spectroscopy and Gas

Chromatography-Mass Spectrometry
Gilbert, J . (ed.) (1987). "Applications of Mass Spectrometry in Food Science." Elsevier Applied
Science, Amsterdam, The Netherlands.
Gudzinowicz, B . J . , Gudzinowicz, M. J . , and Martin, H. F. (1977). "Fundamentals of Integrated

GC-MS" Marcel Dekker, New York.
Karasek, F. W., and Clement, R . E . (1988). "Basic Gas Chromatography-Mass Spectrometry."
Middleditch, B . S. (ed.) (1981). "Practical Mass Spectrometry." Plenum Press, New York.
Millard, B . J . (1979). "Quantitative Mass Spectrometry." Heyden.
Recommended Books on Liquid and High-Performance Liquid

Chromatography
Engelhardt, H. (ed.). (1985). "Practice of High-Performance Liquid ChromatographySprin-

ger-Verlag, New York.
Hamilton, R . J . , and Sewell, P. A. (1977). "Introduction to High-Performance Liquid Chroma-
tography Chapman and Hall, New York.
Horvath, C , ed. (1980). "High-Performance Liquid ChromatographyAcademic Press, New
York.
Pryde, Α., and Gilbert, M. T . (1979). "Application of High-Performance Liquid Chromato-
graphy" Chapman and Hall, New York.
Snyder, L. R . , and Kirkland, J . J . (1979). "Introduction to Modern Liquid Chromatography/'
John Wiley, New Y o r k .
SUBJECT INDEX
Abietic acid quantitative analysis of aromatic constituents

, 3
C - N M R of, 211 of, 2 0 8
dehydrogenation of, 2 0 9 , 212 Azelaic acid
formation of, from wood rosin, 2 0 9 , 211 Ή - N M R of, 31
Ή - N M R of, 211 M S of, 3 2
M S of, 211 preparation of, 3 0
occurrence of, 2 1 0
U V spectrum of, 212
Alkoloids Betulin
biosynthesis of, 2 3 0 allobetulin, formation of, 2 1 5
, 3
classification of, 2 2 9 C - N M R of, 2 1 4
degradation of, 2 2 7 conversion of, to alio- and oxyallobetulin, 213
function of, in plants, 2 2 6 IR spectrum of, 2 1 5
G C of, 2 4 7 IR spectrum o f allobetulin, 215
isolation of, 2 2 6 isolation of, from birch bark, 2 1 4
occurrence of, 2 2 6 M S of, 215
physiological properties of, 2 2 6 occurrence of, 2 1 2
précipitants for, 2 2 7 Bile acids
Amino acids occurrence of, 131
biosynthesis of, 2 5 7 structure of, 1 3 1 - 1 3 2
classification of, 2 5 4 - 2 5 5 Bitter principles
G C of, 2 7 7 o f citrus, removal of, 2 2 0 - 2 2 4
isolectric point of, 2 5 4 ofhops, 68
properties of, 2 5 4 Brucine
n
resolution of, 2 5 6 - C N M R of, 2 4 2
separations of, 2 5 4 Ή - N M R of, 2 4 2
syntheses of, 2 5 5 - 2 5 6 isolation of, from Strychnos nux vomica, 241
Test-tube T L C , 2 8 0 occurrence of, 2 3 8
T L C of, 2 7 3 physiological properties of, 2 3 9
T L C o f carbobenzoxy peptides, 2 8 2
Anthocyanins
alkaline degradation of, 7 Caffeine
, 3
classification of, 6 C - N H R of, 2 3 3
colors of, 7 content of, in tea, 2 3 0
color change of, at various pH values, 1 9 - 2 1 Ή - N M R of, 2 3 2
Aromatic herbs IR spectrum of, 2 3 2
head-space G C of, 2 0 5 - 2 0 8 isolation of, from tea, 2 3 0 - 2 3 2
351
352 Subject Index
Caffeine (continued) Ή - N M R of, 185

occurrence of, 2 3 0 M S of, 185
physiological properties of, 231 synthesis of, 1 8 3 - 1 8 4
T L C o f xanthine derivatives, 2 3 2 U V of, 185
U V spectrum of, 2 3 2 Castor oil
Camphene formation o f azelaic acid from, 3 0 - 3 1
formation of, 194 Ή - N M R of, 3 4
Ή - N M R of, 194 n-heptaldehyde from, 3 2 , 3 3
mechanism o f formation of, 192 hydrolysis of, 3 0
Camphor IR of undecenoic acid, 3 3
formation of, 1 9 2 - 1 9 5 M S o f azelaic acid, 3 4
Ή - N M R of, 195 pyrolysis of, 3 3
U V spectrum of, 195 ricinoleic acid from, 3 0
Capsanthin undecenoic acid from, 33
l 3
C - N M R o f , 112 Cerin
color reactions of, 111 IR of, 2 1 8
Ή - N M R of, 112 isolation of, from cork, 217
isolation of, from paprika, 1 1 0 - 1 1 1 Chlorophyll
M S of, 112 degradation of, 3 0 7
occurrence of, 110 occurrence of, 3 0 6
U V spectrum of, 113 structure of, 3 0 6 , 3 0 8
Carbohydrates Cholesterol
classification of, 7 0 biosynthesis of, 129
, 3 4
column chromatography of, 8 4 C - N M R of A -cholesten-3-one, 153
4
gas-liquid chromatography of, 8 6 A -cholesten-3-one from, 149
5
glucosides of, 8 4 A -cholesten-3-one from, 149
4
H P L C of, 9 0 IR of A -cholesten-3-one, 153
mannoheptulose, 7 9 IR o f A'-cholesten-3-one, 152
4
mutarotation, 7 5 U V o f A -cholesten-3-one, 154
oligosaccharides, 7 6 Column chromatography
thin-layer chromatography of, 8 9 of carbohydrates, on charcoal, 8 4
ß-Carotene of carotenes, 125
column chromatography of, 124 of essential oil, 198
Ή - N M R of, 102
spectroscopic determination of, 125
T L C of, 2 7 3 Ergosterol
Carotenoids irradiation of, 156
biosynthesis of, 109 T L C of, 157
classification of, 1 0 5 - 1 0 8 Essential oil
dehydrogenation of, 108 flash chromatography of, 1 9 8 - 2 0 0
functions of, 109
H P L C of, 120
hydrocarbons, 105 Fatty acids
occurrence of, 105 classification of, 2 3 , 2 4
of oranges, 117 G C of methyl esters, 4 9
syntheses of, 108 isolation of, 2 3
T L C of, 117 reactions of, 2 4 , 2 5
xanthophylls, 1 0 6 - 1 0 8 T L C of, 4 4
Carvone Flavanones
l 3
C - N M R o f , 185 chemical properties of, 5
enantiomers of, 187 Flavonoids
I R o f , 185 alkaline degradation of, 3
Subject Index 353
biosynthesis of, 8 Isoborneol

classification of, 1 , 2 acetate of, 194
interconversion of, 3 mechanism o f formation of, 193
occurrence of, 2 Isoflavones
physiological properties of, 3 alkaline degradation of, 5
Friedelin occurrence of, 5
, 3
C - N M R of, 2 1 9
IR of, 2 2 0
isolation of, from c o r k , 2 1 9
Leucoanthocyanidins
M S of, 2 2 0
occurrence of, 8
occurrence of, 217
Lignans
classification of, 4 8
dehydrogenation of, 4 9
Gas-liquid chromatography
formation of, 4 8
o f alkaloids, 2 4 7
isomerization of, 4 8
of amino acids, 2 7 7
physiological properties of, 5 0
of fatty acid esters, 4 9
Limonene
of steriods, 1 6 1 - 1 6 4
carvacrol from, 1 8 2 , 186
preparation o f methyl esters for, 4 3
carvone from, 1 8 2 , 184
Glucosamine from crustacean shells, 8 2
Ή - N M R of, 184
Glutamine
occurrence of, 182
Ή - N M R of, 2 6 2
photoprotonation of, 1 9 5 - 1 9 8
IR of, 261
Lipids
isolation of, from red beet, 2 6 0 - 2 6 1
classification of, 2 3 - 2 4
occurrence of, 2 5 9
extraction of, 2 3
Glycylglycine
phospholipids, 2 5
Ή - N M R of, 2 7 3
waxes, 2 5
IR of, 2 7 2
Lycopene
syntheses of, 2 6 9 - 2 7 2 , 3
C - N M R o f , 116
color reactions of, 116
Ή - N M R of, 117
Hecogenin
isolation of, from tomatoes, 115
IR of, 148
M S of, 117
occurrence of, 146
occurrence of, 113
transformations of, 147
U V o f , 117
Hesperidin
Lysozyme
acidic degradation of, 12
, 3 derivatives of, 3 2 6
C - N M R o f , 11
IR of, 3 2 6
color tests of, 11
isolation of, from albumen, 3 2 4 - 3 2 5
isolation of, orange peel, 9
properties of, 3 2 4
M S of, 11
occurrence of, 9
physiological properties of, 9
purification of, 10 Mescaline
Hesperitin M S of, 2 4 6
, 3
C - N M R o f , 11 physiological properties of, 2 4 2 - 2 4 3
formation of, 12 syntheses of, 2 4 3 - 2 4 6
U V of, 13 U V of, 2 4 3
Hydroquinone Methyl oleate
of insects, 61 azelaic semialdehyde from, 3 4 - 3 5
IR of, 6 4 ozonization of, 3 4 - 3 5
I L C of, 6 3 - 6 4 pelargonaldehyde from, 3 4 - 3 5
354 Subject Index
Monosaccharides hydrolysis o f by ribonuclease, 2 9 9

anomers, 7 4 isolation o f s R N A from baker's yeast,
branched-chain sugars, 7 2 291-292
configuration of, 71 types of, 2 8 7
degradation o f pentoses, 7 5 Nucleotides
deoxy-sugars, 7 2 cyclic nucleotides enzymatic preparation of,
epimers, 7 2 296-298
fermentation o f starch, 7 3 synthesis of, 2 9 7
furanose form, 7 4 uridine 2 ' , 3 ' - c y c l i c phosphate, 2 9 6
glucosamine, from crustacean shells, 8 2 T L C of, 3 0 0
heptoses, occurrence of, 71 thymidine 3'-phosphate, synthesis of, 2 9 5
hydrazones of, 7 5
mannoheptulose, from avocado, 7 9 - 8 1
mutarotation, 7 5 Oligosaccharides
osazones of, 7 5 - 7 6 classification of, 7 6 - 7 7
osone of, 7 6 glycosides, 7 6
perseitol, from avocado, 7 9 Oxyallobetulin
pyranose form, 7 4 IR of, 2 1 6
Myristic acid preparation of, 2 1 6
IR of, 2 9 Ozonization
preparation of, 2 8 of methyl oleate, 3 4 - 3 6
Myristicin of stigmasterol, 1 4 0 - 1 4 1
dibromo derivative of, 2 9
isolation of, 2 8
M S of, 2 9 Peptides
occurrence of, 2 6 biologically active, 2 5 8
physiological activity of, 2 6 structural determination of, 2 5 7
structure of, 2 5 7
synthesis of, 2 5 8
Naringin ß-Phenylalanine
action o f naringinase on, 15 azlactone synthesis of, 2 6 6 - 2 6 8
bitterness of, 17 Ή - N M R of, 2 6 8
, 3
C - N M R of, 16 IR of, 2 6 8
isolation of, from grapefruit peel, 14 M S of, 2 6 8
naringenin from, 15 syntheses of, 2 8 5
occurrence of, 1 4 - 1 5 Phloroglucinols
Neohesperidin structure of, 6 6
bitterness of, 17 H P L C of, 6 7
Neohesperidin dihydrochalcone in hops, 6 8
synthesis of, 17 Phosphate buffers, 291
sweetness of, 18 α-Pinene
Nucleic acids camphor from, 1 9 4 - 1 9 5
classification of, 2 8 5 mechanism, 1 9 2 - 1 9 3
deoxyribonucleic acid hydrochloride of, 194
structure of, 2 9 0 isolation of, 194
hydrolysis of, 2 8 7 occurrence of, 191
hydrolysis o f nucleotides, 2 8 8 Piperine
, 3
nucleosides of, 2 8 6 C - N M R of, 2 3 5
nucleotides of, 2 8 7 degradation of, 2 3 6 - 2 3 8
purines of, 2 8 6 IR of, 2 3 6
pyrimidines of, 2 8 6 isolation of, from black pepper, 2 3 4 - 2 3 5
ribonucleic acid Ή - N M R of, 2 3 5
hydrolysis o f by alkali, 2 8 8 occurrence of, 2 3 3
Subject Index 355
T L C of, 2 3 5 odor threshold of, 3 4 6

U V of, 2 3 6
Polysaccharides
amylopectin, from potato starch, 9 7 - 1 0 0 Quinones
amylopectin, structure of, 9 5 biosynthesis of, 5 9
amylose, from potato starch, 9 7 - 1 0 0 classification of, 5 4 - 5 9
amylose, structure of, 9 4 Ή - N M R of, 6 5
cellulose, 9 3 IRof,64
chitin, 8 2 , 9 6 , 9 7 M S of, 6 4
dextrans, 9 6 occurrence of,
fermentation o f starch, 9 4 in insects, 5 8 - 5 9 , 6 1 - 6 2
fructans, 9 5 T L C of, 6 3
glycogens, 9 5
heparin, 9 7
hydrolysis o f chitin, 8 2 Rhein
inulin, 9 5 diacetate of, 61
levan, 9 6 isolation of, 6 0
occurrence of, 9 3 occurrence of, 5 9
pectins, 9 6 U V of, 61
plant gums, 9 6 T L C of, 6 0
starch, structure of, 9 4 Ricinoleic acid
wood cellulose, isolation of, 1 0 1 - 1 0 3 from castor oil, 3 0
Porphyrins
biosynthesis of, 3 0 8
degradation o f hemin, 311 Sesamin
degradation o f hemoglobin, 3 0 5 IR of, 5 3
function of, 3 0 4 isolation of, 51
isolation o f hemin, 3 0 9 nitro-derivative of, 5 2
metalloporphyrins from petroleum, 3 1 7 - 3 2 0 occurrence of, 5 0 - 5 1
occurrence of, 3 0 4 - 3 0 5 Sesamolin, 5 0
properties of, 3 0 4 - 3 0 5 Ή - N M R of, 5 2
structure of, 3 0 4 , 3 0 6 IR of, 5 3
T L C o f plant pigments, 315 Steroid hormones
Proteins adrenocortical, 133
classification of, 3 2 1 - 3 2 3 androgens, 134
enzymes, 321 estrogens, 133
isolation of, from groundnuts, 3 2 6 insect molting, 134
occurrence of, 321 Steroids
structure of, 3 2 3 cardiac active, 1 3 4 - 1 3 6
T L C of, 3 2 8 conformation of, 128
Pteridines GCof, 161-164
2-amino-4-hydroxypteridine, U V spectrum occurrence of, 127
of, 3 4 0 sapogenins, 135
isolation of, from fruit fly, 3 3 4 structure of, 1 2 7 - 1 2 8
occurrence of, 3 3 1 - 3 3 2 Sterols
structure of, 3 3 2 of algae, 1 4 2 - 1 4 6
synthesis of, from pyrazines, 3 3 4 determination of, by digitonin, 1 5 9 - 1 6 1
synthesis of, from pyrimidines, 3 3 3 , 3 3 8 G C o f , 161
T L C of, 341 of marine invertebrates, 1 2 9 - 1 3 0
Pyrazines of plants, 130
G C / M S of, 3 4 5 o f yeast, 131
isolation of, 3 4 4 structures of, 129
occurrence of, 3 4 3 T L C of, 1 6 5 - 1 6 7
356 Subject Index
Stigmasterol of nucleotides, 3 0 0
, 3
C - N M R o f , 138 of plant pigments, 315
degradation of, 1 3 9 - 1 4 2 of proteins, 3 2 8
isolation of, from soybean oil, 1 3 7 - 1 3 8 of pteridines, 341
M S of, 139 of steroids, 1 6 5 - 1 6 7
occurrence of, 136 of terpenoids, 2 2 3
U V of, 139 of vitamin D 2, 158
Strychnine Thymidine 3-phosphate
, 3
C - N M R of, 2 4 0 synthesis of, 2 9 3 - 2 9 6
isolation of, from Strychnos nux vomica, 240 Trimyristin
M S of, 241 IR of, 2 8
occurrence of, 2 3 8 isolation of, 2 7
physiological properties of, 2 3 9 M S of, 2 8
U V of, 241 occurrence of, 2 6
saponification of, 2 8
Tyrosine
Tannins, 8 D-tyrosine, from racemic, 2 5 2
Terpenoids racemization of, 2 6 2
classification of, 168 resolution o f racemic, 2 6 4
distribution of, 168
diterpenes,
acyclic, 1 7 4 - 1 7 5 Undecenoic acid
bicyclic, 175 Ή - N M R of, 3 4
monocyclic, 175 IR spectrum of, 3 3
tricyclic, 176 M S of, 3 4
essential oil, extraction of, 187 preparation of, 3 3
monoterpenes Urea inclusion compounds
acyclic, 169 of binary systems of fatty acids, 41
bicyclic, 1 7 1 - 1 7 2 o f cis-trans isomers, 3 9
monocyclic, 170 dissociation temperature of, 4 0
sesquiterpenes of fatty acids, 3 9
acyclic, 172 of petrol, 3 9
azulenes, 174 of saturated and unsaturated acids, 37
bicyclic, 173 structure of, 3 6 - 3 8
monocyclic, 173 o f terpenes, 3 9
triterpenes thiourea inclusion compounds, 3 8
acyclic, 178
biosynthesis of, 181
classification of, 176 Vitamin D 2
1 3
dehydrogenation of, 176 C - N M R o f , 158
pentacyclic, 1 7 9 - 1 8 0 formation of, 1 5 5 - 1 5 7
tetracyclic, 178 Ή - N M R of, 158
Thin-layer chromatography I R o f , 159
impregnation o f plates for, with silver nitrate, M S of, 158
166 T L C of, 157
of alkaloids, 2 5 0 U V of, 158
o f amino acids, 2 7 3 , 2 8 0
of carbobenzoxy peptides, 2 8 2
o f carbohydrates, 8 9 - 9 0 Wine
of carotenoids, 117 aroma constituents, 201
of ergosterol, 157 G C o f aroma of, 2 0 3
of fatty acids, 4 4 grape juice terpenes, 2 0 3
INDEX OF CHEMICAL
COMPOUNDS
Abietic acid, 2 0 9 Azelaic acid, 31

3-Acetoxy-bisnorcholanic acid, 141 Azlactone o f α-benzoylcinnamic acid, 2 6 7
3-Acetoxy-bisnorcholenic acid, 141
iV-Acetyl-D-tyrosine, 2 6 4
N-Acetyl-DL-tyrosine, 2 6 3 Benzaldehyde, 3 4 6
Adenosine diphosphate, 3 0 2 Benzoquinone, 6 3
Adenosine monophosphate, 3 0 2 Benzyl alcohol, 201
Adenosine triphosphate, 3 0 2 Betulin, 2 1 4
Adhumulone, 6 9 Bovin ^-globulin, 3 3 0
α-Alanine, 2 7 9 , 2 8 1 Bovin serum albumin, 3 3 0
ß-Alanine, 2 7 9 Brucine, 241
DL-Alanine Butyric acid, 4 2
Allobetulin, 215
Allobetulin acetate, 2 1 6
Allocholanic acid, 142 Caffeine, 2 3 1 , 2 4 9
Allose, 8 8 Campestanol, 166
ot-Aminobutyric acid, 2 7 9 Campesterol, 166
ß-Aminobutyric acid, 2 7 9 Camphene, 194
7-Aminobutyric acid, 2 7 9 Camphor, 195
2-Amino-4-hydroxypteridine, 3 4 2 Capric acid, 3 9
2-Amino-4-hydroxy-6-methylpteridine, 342 Caproic acid, 3 9 , 4 2
2-Amino-4-hydroxy-7-methylpteridine, 342 Caprylic acid, 3 9 , 4 2
2-Amino-4-hydroxy-6,7-dimethylpteridine, 342 Capsanthin, 111
Amylopectin, 9 7 Carbobenzoxydiglycine, 2 8 4
Amylose, 9 7 Carbobenzoxydigly-OEt, 2 8 4
Androstan-17-one, 163 Carbobenzoxy-DL-alanine, 2 8 4
Androstan-3,17-dione, 163 Carbobenzoxy-DL-dialanine, 2 8 4
Androstane, 163 Carbobenzoxy-DL-phenylalanine, 2 8 4
Anthocyanins, 2 0 Carbobenzoxyglycine, 2 8 4
Arabinose, 8 8 Carbobenzoxytetraglycine, 2 8 4
Arachin, 3 2 7 Carbobenzoxytriglycine, 2 8 4
Arginine, 2 7 6 Carbobenzoxytrigly-OEt, 2 8 4
Asparagine, 2 7 6 Carotene, α, β , 7- 119
Aspartic acid, 2 7 4 , 2 7 9 , 281 Carotene, β- 125
Atropine, 2 4 9 Carvacrol, 182
357
358 Index of Chemical Compounds
Carvone, 1 8 2 , 189 trans-Furan linalool oxide, 201

Carvoxime, 182 Furfural, 3 4 6
Castor oil, 3 2 , 3 3
Cellobiose, 8 8
Cellulose, 103 Galactose, 8 8
Cerin, 2 1 8 Geraniol, 201
Chitin, 8 2 Glucosamine hydrochloride, 8 2
Chlorophyll, 316 Glucose, 1 3 , 8 5 , 8 8 , 8 9 , 9 1
Cholestane, 163 Glutamic acid, 2 7 9
Cholestanol, 1 6 3 , 166 Glutamine, 2 6 0 , 2 7 4
Cholestan-3-one, 163 Glycine, 2 7 9 , 2 8 1 , 2 8 3
Cholestanyl acetate, 163 Glycosides, 2 0 3
Cholestanyl methyl ether, 163 Glycylglycine, 2 8 3
4
A -Cholesten-3-one, 1 5 2 , 163 Guanosine diphosphate, 3 0 2
5
A -Cholesten-3-one, 163 Guanosine monophosphate, 3 0 2
Cholesterol, 151, 160, 1 6 3 , 166 Guanosine triphosphate, 3 0 2
Cholesteryl acetate, 151 Gulose, 8 8
Chondrillasterol, 143
ot-Chymotrypsin, 3 3 0
Cinchonidine, 2 4 8 Hecogenin, 146
Cinchonine, 2 4 8 Hecogenone, 147
Citraurin, 119 Hematinic acid, 3 1 4
Citronellol, 201 Hemin, 313
Cocaine, 2 4 8 Hemoglobin, 3 3 0
Codeine, 2 4 9 , 2 5 1 /î-Heptaldehyde, 3 3
Cohumulone, 6 9 Heptan-2-one, 3 4 6
Conarachin, 3 2 7 Hesperidin, 9 , 10, 11, 12
Coprostane, 163 Hesperitin, 12, 13
Coprostanol, 166 Hexanol, 3 4 6
Corn oil, 3 9 Histidine, 2 7 7
Cryptoxanthin, 119 Homatropine, 2 4 9
Cyanoethylphosphate, 2 9 5 Hotrienol, 201
Cytidine diphosphate, 3 0 2 Humulone, 6 9
Cytidine triphosphate, 3 0 2 Hydrastine, 2 4 9
Cytochrome C , 3 3 0 Hydroquinone, 6 3
Hydroxyproline, 2 7 7
4-Hydroxy-2,5,6-triaminopyrimidine, 3 3 8
5 a , 6 ß - D i b r o m o c h o l e s t a n - 3 - o n e , 151
Digitonin, 160
2,4-Dihydroxypteridine, 3 4 2 Inosine diphosphate, 3 0 2
3,7-Dimethyl-octa-1 -en-3,7-diol, 2 0 4 Inosine monophosphate, 3 0 2
3,7-Dimethyl-octa-l,5-diene-3,7-diol, 2 0 4 Inosine triphosphate, 3 0 2
Drosopterin, 3 3 7 Isoborneol, 194
Isobornyl acetate, 194
Isodrosopterin, 3 3 6
Elaidic acid, 3 9 , 4 0 Isofucosterol, 143
Ergosterol, 1 4 3 , 1 5 5 , 157, 166 Isoleucine, 2 7 4 , 2 7 9 , 281
Essential oils, 199 Isosepiapterin, 3 3 6
Ethylbenzoquinone, 6 5 Isoxanthopterin, 3 4 2
Friedelin, 2 1 9
Fructose, 91
c/s-Furan linalool oxide, 201 2-Keto-bisnorcholanic acid, 142
Index of Chemical Compounds 359
Lactose, 88, 91 Myristicin, 28

Lauric acid, 39, 40
Leucine, 279
Limonene, 162, 196, 346 Narcotine, 249, 251
Limonin, 220 Naringin, 15, 16, 17,220
Linalool, 201, 346 Naringin dihydrochalcone, 17, 18
Linoleic acid, 39, 4 0 , 42 Neodrosopterin, 337
Linolenic acid, 39, 40 Neohesperidin, 9
Linseed oil, 39 Nerol, 201
Lupulone, 69 Nomilin, 220
Lutein, 119 Norleucine, 279
Luteoxanthin, 119 Norvaline, 279
Lycopene, 114
Lysine, 277
Lysozyme, 328, 330 Oleic acid, 39, 40, 42
bromide, 325 Olive oil, 39
carbonate, 325 Ornithine, 279
chloride, 325 Ovalbumin, 330
Ovomucoid, 330
Oxyallobetulin, 216
Macroglobulins, 330 Oxyallobetulin acetate, 216
Maltose, 8 5 , 8 8 3-Oxy-bisnorcholanic acid, 142
Mannoheptulose, 81
Mannoheptulose hexacetate, 81
Mannose, 88 Palmitic acid, 39, 40, 42
Melibiose, 85 Papaverine, 249, 251
Mescaline, 246 Pelargonaldehyde, 35
Mesoporphyrin, 302 Pelargonie acid, 39, 40
Menth-l-ene-9-ol, 201 Pentylfuran, 346
2-Methoxy-2-isobutylpyrazine, 340 Pepsin, 330
Methyl a-arabinoside, 88 Perseitol, 81
Methyl ß-arabinoside, 88 ß-Phenylalanine, 267, 274, 279, 283
Methyl benzoquinone, 65 Phenylethyl alcohol, 201
Methyl elaidate, 39 Phloracetophenone
Methylethylmaleimide, 314 Phytofluene, 119
Methyl a-glucoside, 88 Pilocarpine, 289
Methyl ß-glucoside, 88 Pinene, α-and β-, 194
6-Methylisoxanthopterin, 342 Piperic acid, 237
Methyl a-mannoside, 88 Piperine, 234
Methyl ß-mannoside, 88 Poriferasterol, 143
Methyl oleate, 35, 45 Porphyrins, 319
Methyl salicylate, 346 Proline, 274, 279
Methyl semiazelaaldehyde, 36 Protoporphyrin, 313
Methyl stéarate, 45
Methyl-3,4,5-trimethoxybenzoate, 246
7-Methylxanthopterin, 342 Quinidine, 248
Methyl a-xyloside, 88 Quinine, 248
Methyl ß-xyloside, 88
Monoterpenes, 206
Morphine, 249, 251 Rafiinose, 88, 91
Myoglobin, 330 Ribonuclease, 299, 330
Myristic acid, 28, 39, 40, 42 Ribose, 88
360 Index of Chemical Compounds
Rhamnose, 13, 88, 89 Tridecylic acid, 39, 40

Rhein, 59 3,4,5-Trimethoxybenzoic acid, 244
Ricinoleic acid, 31 3,4,5-Trimethoxybenzyl alcohol, 245
sRNA, 292 3,4,5-Trimethoxybenzyl chloride, 245
Rockogenin, 148 3,4,5-Trimethoxyphenyl acetonitrile, 246
Trimyristin, 27
Tritylthymidine, 295
Scopolamine, 249 Trypsin, 330
Sepiapterin, 336 Tryptophan, 274
Serine, 279 Turpentine oil, 274
Sesame oil, 51 Tyrosine, 263, 274, 277, 279, 281
Sesamin, 52
Sesamolin, 52
ß-Sitostanol, 166 Undecenoic acid, 33
ß-Sitosterol, 163, 166 Urea, 36, 39
ß-Sitosteryl, acetate, 163 Uridine 2',3'-cyclic phosphate, 297
Soybean oil, 39 Uridine diphosphate, 297, 302
Starch, 99 Uridine monophosphate, 297, 302
Stearic acid, 40, 42 Uridine 2'-phosphate, 298
Stigmastane, 163 Uridine triphosphate, 302
Stigmasterol, 137, 138, 141, 163, 163
Stigmasteryl acetate, 141
Strychnine, 240, 249 Valine, 274, 277
Sucrose, 8 5 , 8 8 , 8 9 , 9 1 Violaxanthin, 119
Vitamin D 2, 147
Vitamin D „ 157
Tachysterol, 157
Talose, 88
Thebaine, 249,251 Xylose, 85, 88, 89
Threonine, 277, 279
Thymidine 3-phosphate, 295
Thyroglobulin, 330 Zeaxanthin, 119
Tigogenin, 148

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NATURAL PRODUCTS

ACADEMIC PRESS, INC.

Academic Press, Inc.

United Kingdom Edition published by

Library of Congress Cataloging-in-Publication Data

Ikan, Raphael, date

PRINTED IN THE UNITED STATES OF AMERICA

The syllabus of the practical course in organic chemistry at most universities

Each section of these chapters includes a general introduction and methods of

The flavonoid compounds can be regarded as C 6 - C 3 - C 6 compounds, in which

Flavonoid compounds and the related coumarins usually occur in plants

By spectroscopic measurement it is now possible to determine the

Flavanones may be converted into flavonols and flavones.

Consequently, the carbonyl group of flavone does not react normally

Isoflavones are degraded by alkali as follows:

some of them are potent fish poisons.

The natural anthocyanidins may be classified into three groups: pelargonidin,

Various anthocyanins can be distinguished by partition between two immisci-

Leucoanthocyanidins are flavan-3,4-diols. These colorless substances give red

Flavan-3,4-diols are sometimes obtained by reduction of flavonols of

Biosynthetically, the flavonoid compounds are formed by the combina-

B. Isolation of Hesperidin from Orange Peel

b. Purification of hesperidin with formamide

d. Ferric chloride test

e. Magnesium-hydrochloric acid reduction test

C. Acidic Degradation of Hesperidin

Color with Reagent

Glucose 0.29 brown blue

D. Isolation of Naringin from Grapefruit Peel

E. Synthesis of Naringin Dihydrochalcone—

The relative bitterness of these flavonoids compared to quinine is shown

Alkaline cleavage of ring C of naringin yields the corresponding chal-

Compound Taste Molarity of Iso-Sweet Solution Molarity Weight

0.0045% solution of NDHC is compared with a 5 % solution of sucrose. The

F. Color Changes of Anthocyanins at Various pH Values

b. A similar procedure is adopted for pelargonium and roses.

Test 0ΛΝ 0Λ5Μ 0.15M 0.15M

1 9.5 0.5 — — 2.1

6. Robinson, G. M., and Robinson, R . (1931). Biochem. J. 25, 1687.

1. Name the main groups of flavonoids.

I. Agrawal, P. K. (1989). "Carbon-13 NMR of Flavonoids:' Elsevier,

1. Fats and Oils

A Number of the Natural Fatty Acids

Although most naturally occurring fatty acids are straight-chain

Chlorine and iodine, or iodine chloride may be added in a similar

Ozone adds to the double bonds of unsaturated acids, forming an

Β. Isolation of Trimyristin and Myristicin from Nutmeg

Nutmeg oil is used mainly in food flavoring, and to a lesser extent in

d. Infrared spectrum (IR) (in CS 2)

f. Thin-layer chromatography of nutmeg constituents

h. Preparation of dibromo myristicin

i. IR spectrum of myristic acid (in CS 2)

1. de Stevens, G . , and Nord, F. F . (1955). Natural phenylpropane derivatives. In "Modern

C. Preparation of Azelaic Acid from Castor Oil

D. Formation of n-Heptaldehyde and Undecenoic Acid

E. Ozonization of Methyl Oleate

followed by catalytic hydrogénation in methanol (5). Recent studies of the

12 g has been introduced, the temperature being maintained at 30 to 35°C by

F. Preparation of Urea Inclusion Compounds