58861-72-6Relevant articles and documents
One-Step Conversion of Methyl Ketones to Acyl Chlorides
Zaragoza, Florencio
, p. 10370 - 10374 (2015/11/03)
Treatment of aromatic and heteroaromatic methyl ketones with sulfur monochloride and catalytic amounts of pyridine in refluxing chlorobenzene leads to the formation of acyl chlorides. Both electron-rich and electron-poor aryl methyl ketones can be used as starting materials. The resulting C1-byproduct depends on the precise reaction conditions chosen.
α-Oxo- and α-Thioxothioamides from Methyl Ketones
Adiwidjaja, Gunadi,Guenther, Horst,Voss, Juergen
, p. 1116 - 1132 (2007/10/02)
Mixtures of α-(chloro)sulfenyl chlorides 5 and trisulfides 6 are obtained from the reaction of thionyl chloride with methyl ketones in the presence of pyridine.From these mixtures as well as from the pure trisulfides 6, with amines the α-oxothioamides 1-4
Phenyl sulfonyl, benzylthiochloromethanes
-
, (2008/06/13)
Alpha,alpha-dichloro-methane-sulfenyl chlorides and alpha-chloromethylbenzyl sulfides useful as herbicides and chemical intermediates for herbicides and their method of manufacture.