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    The document describes a study examining the use of 3-nitrobenzeneboronic acid (1) as a novel, mild, and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions. The researchers found that various alcohols and phenols could be efficiently acetylated with acetic anhydride in good to excellent yields at room temperature using just 2.5 mol% of catalyst 1. The reactions proceeded cleanly and selectively even for sensitive functional groups. Comparative studies showed catalyst 1 performed the acetylations more selectively and at lower catalyst loadings than other catalysts such as indium triflate and lithium perchlorate.

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    The document describes a study examining the use of 3-nitrobenzeneboronic acid (1) as a novel, mild, and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions. The researchers found that various alcohols and phenols could be efficiently acetylated with acetic anhydride in good to excellent yields at room temperature using just 2.5 mol% of catalyst 1. The reactions proceeded cleanly and selectively even for sensitive functional groups. Comparative studies showed catalyst 1 performed the acetylations more selectively and at lower catalyst loadings than other catalysts such as indium triflate and lithium perchlorate.

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    The document describes a study examining the use of 3-nitrobenzeneboronic acid (1) as a novel, mild, and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions. The researchers found that various alcohols and phenols could be efficiently acetylated with acetic anhydride in good to excellent yields at room temperature using just 2.5 mol% of catalyst 1. The reactions proceeded cleanly and selectively even for sensitive functional groups. Comparative studies showed catalyst 1 performed the acetylations more selectively and at lower catalyst loadings than other catalysts such as indium triflate and lithium perchlorate.

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    1 s2.0 S0040403906014444 Main PDF

    Uploaded by

    Prasanth Bitla
    The document describes a study examining the use of 3-nitrobenzeneboronic acid (1) as a novel, mild, and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions. The researchers found that various alcohols and phenols could be efficiently acetylated with acetic anhydride in good to excellent yields at room temperature using just 2.5 mol% of catalyst 1. The reactions proceeded cleanly and selectively even for sensitive functional groups. Comparative studies showed catalyst 1 performed the acetylations more selectively and at lower catalyst loadings than other catalysts such as indium triflate and lithium perchlorate.

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    of 3

    Tetrahedron Letters 47 (2006) 72637265

    A novel 3-nitrobenzeneboronic acid as an extremely mild and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions
    R. H. Tale* and R. N. Adude
    School of Chemical Sciences, S.R.T.M. University, Nanded 431606, Maharashtra, India
    Received 20 March 2006; revised 27 June 2006; accepted 10 July 2006 Available online 17 August 2006

    AbstractA novel 3-nitrobenzeneboronic acid is found to catalyse eciently the acetylation of a wide range of alcohols as well as phenols with acetic anhydride in good to excellent yields at room temperature under solvent-free conditions. The reactions are clean and the catalyst is mild such that highly sensitive functional groups including oximes are stable to the reaction conditions. 2006 Elsevier Ltd. All rights reserved.

    With increasing environmental concerns and the regulatory constraints faced in the chemical and pharmaceutical industries, the development of environmentally benign organic reactions has become a crucial and demanding area in modern organic chemical research.1 According to Wender, the ideal synthesis is one in which the target components are readily obtained in one step and in quantitative yields from readily available starting materials in an environmentally acceptable process.2 Acetylation of alcohols is an important and common transformation in organic synthesis.3 In general, acetyl chloride or acetic anhydride, in the presence of a tertiary amine such as triethylamine or pyridine, is used for the acetylation of alcohols.4 For practical reasons, the latter is usually preferred. The use of 4(dimethylamino)pyridine (DMAP)5 as a co-catalyst accelerates the acetylation process. However, to overcome the problems associated with these basic catalysts, the use of Bu3P for acetylation of base sensitive alcohols was reported by Vedjes et al.6 In addition, protic and Lewis acids, and on some occasions, solid acids have also been reported to be eective for catalysing the acetylation of alcohols.7 In view of the synthetic importance of this reaction, a plethora of catalysts for acetylation have been introKeywords: 3-Nitrobenzeneboronic acid; Solvent-free reaction; Acetylation; Deoximation. * Corresponding author. Fax: +91 2462 29245; e-mail: rkht2002@ yahoo.com 0040-4039/$ - see front matter 2006 Elsevier Ltd. All rights reserved. doi:10.1016/j.tetlet.2006.07.046

    duced including simple metal salts such as COCl2,8 ZnCl2,9 TiCl4AgClO4,10 Me3SiCl,11 LiClO412 and MgClO413 as well as metal triates such as Sc(OTf)3,14 Me3SiOTf,15 In(OTf)3,16 Cu(OTf)317 and Bi(OTf)3.18 Recently, perchlorates were reported to catalyse the acetylation of alcohols, however, perchlorates, particularly of lithium, are reported to be explosive and moisture sensitive. Very recently, molecular iodine catalysed acetylation of alcohols was reported.19 Although a large number of methods for acetylation are available, the practical applicability of most of these methods suers from limitations such as the use of, (1) expensive, moisture sensitive and toxic catalysts, (2) long reaction times and (3) a lack of generality. In view of the modern demands of organic synthesis,1 there is still the need to develop an ecient, mild and environmentally benign protocol for the acetylation of alcohols. In recent years, we have been engaged in evaluating the catalytic potential of arylboronic acids, particularly those with electron withdrawing substituents, in organic synthesis.20 We reported that 3-nitrobenzeneboronic acid 1 eciently catalysed the selective transesterication of b-ketoesters under mild conditions.21 We reasoned that, catalyst 1, might also activate anhydrides for acetylation of alcohols. Herein, we report that various alcohols can be acetylated with acetic anhydride eciently, in good to excellent yields, in the presence of 1 (2.5 mol %) at room temperature under solvent-free conditions (Scheme 1).

    7264
    B(OH)2 O2N

    R. H. Tale, R. N. Adude / Tetrahedron Letters 47 (2006) 72637265

    R-OH

    (2.5mol%) R-OAc

    Ac2O (3-10 equiv.), R.T.

    Scheme 1.

    Table 1. Acetylation of n-decanol with acetic anhydride catalysed by 1a Entry 1 2 3 4 5


    a b

    Catalyst (mol %) 1.0 1.5 2.0 2.5 2.5

    Time (h) 10 10 10 10 7

    Yieldb (%) 42 56 78 90 95c

    All the products gave satisfactory spectral data (IR, 1H NMR). Isolated yield. c 0.2 equiv of MgSO4 was added.

    In order to establish the best reaction conditions, we performed an optimisation study using n-decanol as the model substrate in the presence of varying amounts of catalyst 1, might also activate anhydrides for acetylation of alcohols. As shown in Table 1, 2.5 mol % of catalyst was found to be eective for acetylation of n-decanol in 95% yield within 7 h. A threefold excess of acetic anhydride was eective for the reaction to proceed at a reasonable rate. To explore the generality and scope of the method, other alcohols and phenols were acetylated with acetic anhydride using our optimised reaction conditions. The results are collected in Table 2. Structurally diverse alcohols such as primary, secondary, allylic and propargylic alcohols underwent smooth acetylation in good to excellent yields and, in some cases, in quantitative yields. Notably, hindered tertiary alcohols such as 1-methylcyclohexanol and adamantanol (entries 5 and 6) were acetylated cleanly and eciently under the present reaction conditions in high

    Table 2. Acetylation of alcohols and phenols catalysed by 3-nitrobenzeneboronic acid 1a Entry 1 2 3 4 5


    OH OAc

    Substrate n-C10H21OH n-C8H17OH Benzyl alcohol 4-Nitrobenzyl alcohol

    Product n-C10H21OAc n-C8H17OAc Benzyl acetate 4-Nitrobenzyl acetate

    Time (h) 7 6 10 12 14

    Yieldb (%) 95 90 90 94 86

    OH

    16
    OAc

    89

    7
    Me

    OH Me OH OH Ph OAc

    OAc

    14

    97

    8 9 10

    Ph

    OAc

    11 14 12

    95 91 >99c

    Ph2CHOH
    O Ph OH

    Ph2CHOAc2
    O Ph Ph OAc

    11

    Ph

    17

    >99c

    12 13

    Cholesterol
    OH O

    Cholesterol acetate
    OAc O OH O2N
    HON OH OAc

    15 10

    >99d 92

    14

    O2N
    HON

    OAc

    90

    15
    a

    12

    95d

    All the reactions were performed using 3 equiv of acetic anhydride unless otherwise stated. Isolated yields. c To solubilise solid alcohol, 5 equiv of acetic anhydride was added. d The reactions were performed using 10 equiv of acetic anhydride.
    b

    R. H. Tale, R. N. Adude / Tetrahedron Letters 47 (2006) 72637265 Table 3. Selective acetylation of 4-hydroxyacetophenone oxime using various catalystsa Entry 1 Catalyst Time (h) Selectivityb (%) 95

    7265

    B(OH)2

    12

    NO2
    2 3
    a

    in Table 2. After completion, the reaction was quenched with water (20 cm3). The mixture was extracted with ethyl acetate (2 30 cm3) and the combined organic layer was washed with saturated NaHCO3 (2 20 cm3) and brine (20 cm3). Evaporation of the solvent followed by purication by column chromatography (silica gel, eluent, ethyl acetatehexane 1:9) gave the pure acetate.

    In(OTf)3c LiClO4

    0.1 22

    0 82

    All reactions were performed using 5 equiv of acetic anhydride in the presence of 2.5 mol % of the catalyst at room temperature. b Isolated yield of 4-acetyloxyacetophenone oxime. c 4-Acetyloxyacetophenone was obtained as the only product within 5 min.

    Acknowledgement The authors are grateful to the University Grants Commission (UGC), India, for nancial support.

    yields. Moreover, acid sensitive alcohols such as furfuryl alcohol (entry 13) were acetylated in excellent yields without giving any side products. The reaction can also be applied to the acetylation of phenols. The extremely mild behaviour of catalyst 1 was evident from the fact that the acetylation of 4-hydroxyacetophenone oxime (entry 15) was achieved in high yield with no deprotection observed at all. To expand the scope of the present reaction further, we performed a comparative study in which the selective acetylation of 4-hydroxyacetophenone oxime using our catalyst was compared with In(OTf)3 and LiClO4 under solvent-free conditions. The results are collected in Table 3. Indium triate catalysed the acetylation (Table 3, entry 2) extremely fast and the reaction was complete within 5 min, but only with concomitant deprotection of the oxime to give the corresponding 4-acetyloxyacetophenone as the only product. However, acetylation using LiClO4 (Table 3, entry 3) gave comparable selectivity, however, the reaction took longer to reach completion. Although the rate of acetylation with 1 is less than those catalysed by expensive metal triates, it is faster than those involving catalysts (1020 mol %) such as LiClO4, and NBS, and gives comparable yields of products despite using only 2.5 mol % of the catalyst. Unfortunately, all attempts to acetylate diols by this method proved fruitless. The probable reason for this failure is that the catalyst might be trapped by the diol as boronic acids react readily with diols to form 1,3,2dioxaborolanes. Arylboronic acids are usually crystalline solids, stable to air and moisture. Such evidence as exists, indicates that they are of relatively low toxicity [benzeneboronic acid, LD50, oral rat = 740 mg/kg] and have low environmental impact. Moreover, a small amount of boronic acid 1 (2.5 mol %) is eective as a catalyst for the acetylation of alcohols and phenols. General procedure for the acetylation of alcohols and phenols: A mixture of the alcohol or phenol (2 mmol), acetic anhydride (310 mmol) and catalyst 1 (0.025 mmol) was stirred at room temperature for the time indicated

    References and notes


    1. Anastas, P.; Williamson, T. Green Chemistry, Frontiers in Benign Chemical Synthesis and Procedures; Oxford Science Publications: Oxford, 1998. 2. Wender, P. A.; Handy, S. L.; Wright, D. L. Chem. Ind. (London) 1997, 765. 3. Green, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 3rd ed.; John Wiley and Sons: New York, 1999, p 150. 4. Larock, R. C. Comprehensive Organic Transformations; VCH: New York, 1989, p 980. 5. Steglich, W.; Hoe, G. Angew. Chem., Int. Ed. Engl. 1969, 8, 981. 6. Vedjes, E.; Bennett, N. S.; Conn, L. M.; Diver, S. T.; Gingras, M.; Lin, S.; Oliver, P. A.; Peterson, M. J. J. Org. Chem. 1993, 58, 7286. 7. Iqbal, J.; Srivastava, R. R. J. Org. Chem. 1992, 57, 2001. 8. (a) Backer, R. H.; Bordwell, F. G. Org. Synth. 1955, 3, 141; (b) Miyashita, M.; Shiina, I.; Miyoshi, S.; Mukaiyama, T. Bull. Chem. Soc. Jpn. 1993, 66, 1516. 9. Kumareswaran, R.; Gupta, A.; Vankar, Y. D. Synth. Commun. 1997, 27, 277. 10. Nakae, Y.; Kusaki, I.; Sato, T. Synlett 2001, 1584. 11. Bartoli, G.; Bosco, M.; Dalpozzo, R.; Marcantoni, E.; Massaccesi, M.; Rinaldi, S.; Sambri, L. Synlett 2003, 39. 12. Ono, F.; Negoro, R.; Sato, T. Synlett 2001. 13. Ishihara, K.; Kubota, M.; Kurihara, H.; Yamamoto, H. J. Org. Chem. 1996, 61, 4560. 14. Procopiou, P. A.; Baugh, S. P. D.; Flack, S. S.; Inglis, G. G. A. J. Org. Chem. 1998, 63, 2342. 15. Chauhan, K. K.; Frost, C. G.; Love, I.; Waite, D. Synlett 1999, 1743. 16. Chandra, K. L.; Saravanan, P.; Singh, R. K.; Singh, V. K. Tetrahedron 2002, 58, 1369. 17. (a) Orita, A.; Tanahashi, C.; Kakuda, A.; Otera, J. Angew. Chem., Int. Ed. 2000, 39, 2877; (b) Orita, A.; Tanahashi, C.; Kakuda, A.; Otera, J. J. Org. Chem. 2001, 66, 8926. 18. (a) Schumacher, J. C. PerchloratesTheir Properties, Manufacture and Use. In ACS Monograph Series; Reinhold: New York, 1996; (b) Long, J. Chem. Health Saf. 2002, 9, 12. 19. Phukan, P. Tetrahedron Lett. 2004, 45, 4785. 20. (a) Tale, R. H.; Patil, K. M. Tetrahedron Lett. 2002, 43, 9715; (b) Tale, R. H.; Patil, K. M.; Dapurkar, S. E. Tetrahedron Lett. 2003, 44, 3427; (c) Sagar, A. D.; Tale, R. H.; Adude, R. N. Tetrahedron Lett. 2003, 44, 7140. 21. Tale, R. H.; Sagar, A. D.; Adude, R. N.; Santan, H. D. Synlett 2006, 417.

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