Insertion of dimethylsilylene into OH and NH single bonds

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Abstract

Dimethylsilylene, generated by photolysis of dodecamethylcyclohexasilane, inserts efficiently into OH single bonds of alcohols to yield alkoxydimethylsilanes. Use of ethanol-O-d1 yields ethoxydimethylsilane-Si-d1. Dimethylsilylene also inserts into OH single bonds of water or D2O to yield respectively tetramethyldisiloxane or tetramethyldisiloxane-Si2-d2. Dimethylsilylene also inserts into NH bonds of primary and secondary amines to yield aminodimethylsilanes. This reaction provides an efficient route to difunctional silanes. © 1980.

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Yang Gu, T. yin, & Weber, W. P. (1980). Insertion of dimethylsilylene into OH and NH single bonds. Journal of Organometallic Chemistry, 184(1), 7–11. https://doi.org/10.1016/S0022-328X(00)94358-4

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