Facile and Efficient Synthesis of Ethyl 3-oxo-3-(pyridin-4-yl)-2-((pyridin-4-yl)methylene)propanoate
Corresponding Author(s) : Ramazan Erenler
rerenler@gop.edu.tr
Asian Journal of Chemistry,
Vol. 23 No. 8 (2011): Vol 23 Issue 8
Abstract
The refluxing of ethyl isonicotinate with sodium ethoxide and ethyl acetate yielded the ethyl-3- oxo-3-(pyridin-4-yl)propanoate which was in equilibrium with enol form. The desired product, ethyl 3-oxo-3-(pyridin-4-yl)-2-((pyridin-4-yl)methylene)propanoate was synthesized by the treatment of ethyl-3-oxo-3-(pyridin-4-yl)propanoate and its enolic form with the isonicotinaldehyde under the reflux in neat condition.
Keywords
Pyridine derivatives
Ethyl-3-oxo-3-(pyridin-4-yl)-2-((pyridin-4-yl)methylene)- propanoate
Erenler, R. (2011). Facile and Efficient Synthesis of Ethyl 3-oxo-3-(pyridin-4-yl)-2-((pyridin-4-yl)methylene)propanoate. Asian Journal of Chemistry, 23(8), 3763–3764. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/10719
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