Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16837
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dc.contributor.authorYadav, Vasanti G-
dc.contributor.authorChandalia, S B-
dc.date.accessioned2013-04-07T05:28:19Z-
dc.date.available2013-04-07T05:28:19Z-
dc.date.issued1999-01-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/16837-
dc.description19-23en_US
dc.description.abstractMethyl, 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.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJCT Vol.06(1) [January 1999]en_US
dc.titleAn efficient method for synthesis of 2-ethyl hexyl-4-methoxy cinnamate: A raw material for cosmetic industryen_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.06(1) [January 1999]

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