An efficient and rapid microwave-assisted synthesis of 1-acetyl-1H-indol-3-YL acetates
Data(s) |
28/12/2015
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Resumo |
An efficient and rapid synthesis of 1-acetyl-1H-indol-3-yl acetate 1 and its derivatives 7 via the microwave-assisted cyclisation and decarboxylation of 2-[(carboxymethyl)amino]benzoic acids 5 is described. The latter were left to react with acetic anhydride using triethylamine as the base and were subjected to microwave irradiation for 1 minute, at 80 °C with initial power of 300 W. The target 1-acetyl-1H-indol-3-yl acetate 1 and derivatives 7 were isolated in 34-71% yield. In particular, synthesis of 1-acetyl-6-(trifluoromethyl)-1H-indol-3-yl acetate 7f and 1-acetyl-3-methyl-1H-indol-3-yl acetate 7h is reported for the first time. |
Formato |
text |
Identificador |
http://centaur.reading.ac.uk/51462/3/Helen%20Osborn%20Current%20Microwave%20Chemistry.pdf Osborn, H. M. <http://centaur.reading.ac.uk/view/creators/90000179.html>, Brazier, J. A. <http://centaur.reading.ac.uk/view/creators/90001010.html>, Bovill, R. and Parshotam, J. P. (2015) An efficient and rapid microwave-assisted synthesis of 1-acetyl-1H-indol-3-YL acetates. Current Microwave Chemistry, 3. ISSN 2213-3364 doi: 10.2174/2213335603666160108001556 <http://dx.doi.org/10.2174/2213335603666160108001556> (In Press) |
Idioma(s) |
en |
Publicador |
Bentham |
Relação |
http://centaur.reading.ac.uk/51462/ creatorInternal Osborn, Helen M. creatorInternal Brazier, John A. 10.2174/2213335603666160108001556 |
Tipo |
Article PeerReviewed |