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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1998 Volume 8, Issue 5, Pages 185–186 (Mi mendc4718)

This article is cited in 2 papers

Reaction of thioacetic acid with ethenyl- and ethynyl chlorides

S. G. Dyachkovaa, E. A. Beskrylayaa, A. I. Albanova, L. M. Sinegovskayaa, A. G. Malkinaa, T. A. Skotheimb, B. A. Trofimova

a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b Moltech Corporation, Tucson, Arizona, USA

Abstract: Thioacetic acid (TAA) has been subjected to dichlorovinylation with trichloroethene (TCE) under free-radical conditions to form 1-acetylthio-2,2-dichloroethene 1 (yield 70%) which reacts with TAA at room temperature under phase-transfer catalysis conditions to afford a mixture of E- and Z-isomers of 1,2-bis(acetylthio)-2-chloroethene 2 (total yield 71%); ethylthio(chloro)ethyne with sodium thioacetate gives acetylthio(ethylthio)ethyne 3.

Language: English

DOI: 10.1070/MC1998v008n05ABEH000992



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