One-Pot Stereoselective Synthesis of Dimethyl-(Z)-2- (ethanimidoylsulfanyl)-2-butenedioate from Dimethyl Acetylendicarboxylate and Thioacetamide
Corresponding Author(s) : HAMID ARJMANDFAR
h110arj@yahoo.com
Asian Journal of Chemistry,
Vol. 19 No. 2 (2007): Vol 19 Issue 2
Abstract
Thioacetamide reacts with dimethyl acetylenedicarboxylate in acetone to form dimethyl-(Z)-2-(ethanimidoylsulfanyl)-2-butenedioate. Dipotassium hydrogen phosphate powder was found to catalyze the reaction in solvent-free conditions at 90ºC in 1 h.
Keywords
Acetylenic ester
Michael addition
Dipotassium hydrogen phosphate
Solvent-free conditions
Catalyst
(1)
ARJMANDFAR, H.; NAMJOU, N.; RAMAZANI, A. One-Pot Stereoselective Synthesis of Dimethyl-(Z)-2- (ethanimidoylsulfanyl)-2-Butenedioate from Dimethyl Acetylendicarboxylate and Thioacetamide. ajc 2010, 19, 1565-1566.
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