Bulletin of the Chemical Society of Japan p. 287 - 289 (1994)
Update date:2022-09-26
Topics:
Kunai, Atsutaka
Ueda, Takafumi
Toyoda, Eiji
Ishikawa, Mitsuo
Electrolytic reduction of dichloromethylphenyl-, dichlorodiphenyl-, dichloro-o-tolyl-, and dichlorodi-p-tolylsilanes in the presence of 2,3-dimethylbutadiene afforded 1-methyl-1-phenyl-, 1,1-diphenyl-, 1,1-di-o-tolyl-, and 1,1-di-p-tolyl-3,4-dimethyl-1-silacyclopent-3-ene, respectively, while the similar reaction of chloromethyldiphenylsilane with 2,3-dimethylbutadiene afforded 1-(methyldiphenylsilyl)- and 1,4-bis(methyldiphenylsilyl)-2,3-dimethyl-2-butene.A reaction mechanism leading to these products has been discussed.
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