W. Dolling et al., CYCLOCONDENSATION OF O-ETHYL-S-SUBSTITUTED DITHIOCARBONATES TO NEW 4-ALKYLTHIO-1,3-DITHIOL-2-THIONES USING CARBON-DISULFIDE, Phosphorus, sulfur and silicon and the related elements, 83(1-4), 1993, pp. 223-231
lkylthio-5-(p-nitro-phenyl)-1,3-dithiole-2-thiones 4a-e, 4-alkylthio-5
-(p-, bzw. o-cyano-phenyl)-1,3-dithiole-2-thiones 4f, 4g, 4-alkylthio-
5-pivaloyl-1,3-dithiole-2-thiones 4h-j und 5-methylthio-2-thioxo-1,3-d
ithiole-4-carboxylic acid N-methyl-p-chlor- bzw. -p-methoxy-anilides 4
k, 4l are obtained by reaction of the O-ethyl-S-substituted dithiocarb
onates 3 with carbon disulfide/potassium tert. butoxyde in dry DMF and
alkylation reagent. Treatment of 1,3-dithiole-2-thiones 4a-c with mer
curic acetate give 1,3-dithiole-2-ones 5a-c. Carbonyl stretching frequ
encies of 2-oxo-substituted five-membered heterocycles I are discussed
.