Abstract
The oxides of ethylene and propene, and epichlorohydrin, react with thionylanilines (ArN=S=O) in the presence of tetraethylammonium bromide catalyst at 95°–100° C to give N-arylalkeneamidosulfites, whose structures are confirmed by retrosynthesis from the corresponding N-phenylamino alcohols, and thionyl chloride, as well as by their IR spectra.
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