A new direct synthesis of cinnamic acids from aromatic aldehydes and aliphatic carboxylic acids in the presence of sodium borohydride
Cinnamic acids have been prepared in 59–86% yields by a new direct synthesis from aromatic aldehydes and aliphatic carboxylic acids in the presence of sodium borohydride and N-methyl-2-pyrrolidinone (NMP) as solvent, at reflux (185–190°C), for 9–12 hours. Without sodium borohydride, this reaction is...
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Published in: | Tetrahedron letters Vol. 44; no. 17; pp. 3579 - 3580 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier Ltd
21-04-2003
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Online Access: | Get full text |
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Summary: | Cinnamic acids have been prepared in 59–86% yields by a new direct synthesis from aromatic aldehydes and aliphatic carboxylic acids in the presence of sodium borohydride and
N-methyl-2-pyrrolidinone (NMP) as solvent, at reflux (185–190°C), for 9–12 hours. Without sodium borohydride, this reaction is not possible.
A novel approach for synthesis of cinnamic acids in the presence of sodium borohydride, as a very effective alternative to the classical Perkin synthesis is reported. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/S0040-4039(03)00529-X |