Alkaline cleavage of certain phenyl- and chlorine-substituted (halomethyl)disilanes
作者:Kohei Tamao、Makoto Kumada
DOI:10.1016/s0022-328x(00)87518-x
日期:1971.8
The action of sodiumethoxide in ethanol on a number of(halomethyl)disilanes containing phenyl groups or chloride atoms on silicon has been studied. The reaction proceeds in three directions: intramolecular rearrangement involving migration of a silyl group from silicon to carbon, cleavage of the siliconsilicon bond with concomitant reduction of the halomethyl group to methyl, without evolution of