A convenient preparation of arylthioynamines.

T Nakai, K Tanaka, H Setoi, N Ishikawa

文献索引：Nakai,T. et al. Bulletin of the Chemical Society of Japan, 1977 , vol. 50, p. 3069 - 3070

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被引用次数: 31

摘要

(2, 2, 2-Trifluoroethylthio) benzenes prepared from sodium thiolates and 2, 2, 2-trifluoroethyl p-toluenesulfonate reacted with 3 equiv of lithium dialkylamides in diethyl ether to give arylthioynamines in good yields. The present procedure gives good results with aliphatic sulflde.