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Potassium carbonate: a highly efficient catalyst for the acylation of alcohols, phenols and thiols under mild conditions | ||
| Iranian chemical communication | ||
| مقاله 5، دوره 2، Issue 1, pp. 1-81, Serial No. 2، فروردین 2014، صفحه 39-47 اصل مقاله (239.19 K) | ||
| نوع مقاله: Original Research Article | ||
| نویسندگان | ||
| Mostafa Kazemi* 1؛ Homa Kohzadi2؛ Zahra Noori2 | ||
| 1methodology | ||
| 2chemistry | ||
| چکیده | ||
| A general, mild and efficient protocol has been developed for the synthesis of esters and thioesters. The process has been taking place using tetra n-butylammonium iodide (TBAI) as a phase-transfer catalyst and in the presence of potassium carbonate (K2CO3). A wide range of esters and thioesters was prepared in high yields and suitable times by the treatment of alcohols, phenols and thiols with acetic anhydride. Acylation reactions of a number of alcohols, phenols and thiols with acetic anhydride demonstrated that Potassium carbonate is a convenient and efficient catalyst for the synthesis of esters and thioesters. This is a mild, general and practical procedure for the synthesis of esters and thioesters in high yields and suitable times. | ||
| کلیدواژهها | ||
| acylation؛ esters؛ thioesters؛ tetra n-butylammonium iodide؛ potassium carbonate؛ acetic anhydride | ||
| اصل مقاله | ||
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| مراجع | ||
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[1] J. Ko, J. Ham, I.Yang, J. Chin, S.J. Nam, H. Kang, Tetrahedron Lett., 2006, 47, 7101–7106.
[2] J.L.Yu, H. Wang, K.F. Zou, J.R .Zhang, X. Gao, D.W. Z.T. Li. Zhang, Tetrahedron, 2013, 69,310–315.
[3] A. Vakalopoulos, X. Kavazoudi, J. Schoof, Tetrahedron Lett., 2006,47, 8607–8610.
[4] A.B. Naidu, G. Sekar, Tetrahedron Lett., 2008, 49, 3147–3151.
[5] A. Kamal, M. N. A. Khan, K. S. Reddy, Y.V.V. Srikanth, T. Krishnaji, Tetrahedron,2007,48, 3813–3818.
[6] C. Peppe, L.B.D. Castro, J. Can, Chem., 2009, 87, 678-683.
[7] M.M. Lakouraj, B. Movassagh, Z. Fadaei, Monat. Chem., 2002, 133, 1085-1088.
[8] D.S. Kanta, Tetrahedron Lett., 2004, 45, 2919–2922.
[9] A. Orita, C. Tanahashi, A. Kakuda , J OteraAngewChemInt Ed., 2000, 39, 2877-2879.
[10] S.V. Pansare, M.G. Malusara, A.N. Rai, Synth Commun ., 2000, 30, 2587-2592.
[11] B.C. Ranu, P. Dutta, A. Sarkar, J Chem Soc Perkin Trans., 2000, 1, 2223-2225.
[12] S.T.A. Shah, K.M. Khan, H. Hussain, M.U. Anwar, M. Fecker,Tetrahedron,2005, 61, 6652-6656.
[13] S.T.A. Shah, K.M. Khan, A.M. Heinrich, W. Voelter, Tetrahedron Lett., 2002, 43, 8281-8283.
[14] S.G. Lee, J.H. Park, J MolCatal A. Chem., 2003,194, 49-52.
[15] M. Kazemi, Z. Noori, H. Kohzadi, M. Sayadi, A. Kazemi, Iranian Chemical Communication, 2013, 1, 20-25.
[16] S.T. Kadam, H. Lee, S.S. Kim, Bull. Korean Chem. Soc.,2009,30, 1071–1076.
[17] P.R. Gustavo, O. Danirel, C. Bennardi, A. Juan, T.B. Auyinograciel, J.T. Horacio, E-journal of chemistery., 2008, 5, 541-547.
[18] G. Rina, Tetrahedron, 2005, 46, 147–151.
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