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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Yadav, Vasanti G | - |
| dc.contributor.author | Chandalia, S B | - |
| dc.date.accessioned | 2013-04-07T05:28:19Z | - |
| dc.date.available | 2013-04-07T05:28:19Z | - |
| dc.date.issued | 1999-01 | - |
| dc.identifier.issn | 0975-0991 (Online); 0971-457X (Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16837 | - |
| dc.description | 19-23 | en_US |
| dc.description.abstract | Methyl, ethyl and isopropyl esters of 4-methoxy cinnamic acid could be synthesized by Claisen condensation of anisaldehyde with the respective alkyl acetate at a temperature of 0- 5°C using stoichiometric amount of sodium and a few drops of methanol, the latter being used as an initiator. The yield of the ester of cinnamic acid was about 77%. When the reaction was extended to the synthesis of 2-ethylhexyl ester of cinnamic acid, the reaction rates were rather very poor and it was necessary to carry out the reaction at the temperature of 28°C which resulted in the extensive hydrolysis of the starting acetate and the product ester. In the case of 2-ethyl hexyl ester, therefore, it may be desirable to resort to the synthesis of ethyl/methyl-ester of the cinnamic acid by Claisen condensation followed by transesterification of the ethyl/methyl ester.Thus, transesterification of ethyl 4-methoxy cinnamate with excess of 2-ethyl hexanol and p-toluenesulfonic acid as catalyst at 150°C gave a yield of 93% in 6 h. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJCT Vol.06(1) [January 1999] | en_US |
| dc.title | An efficient method for synthesis of 2-ethyl hexyl-4-methoxy cinnamate: A raw material for cosmetic industry | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJCT Vol.06(1) [January 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCT 6(1) 19-23.pdf | 1.14 MB | Adobe PDF | View/Open |
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