Abstract

Abstract Reactions of tert-butyl (chloro) dimethylsilane with primary and secondary amines or their lithium salts produce compounds having the general formula t-BuMe2SiNRR1. These compounds are distillable liquids that show high stabilities toward hydrolysis. Their chemical reactivities are generally lower than their trimethylsilyl analogs. tert-Butyldimethylsilyl (trimethylsilyl)-benzylamine, C6H5CH2N(SiMe2 t-Bu)SiMe3, is readily made by lithiation and subsequent silylation of C6H5CH2NHSiMe2 t-Bu but cannot be prepared with similar ease from trimethylsilylbenzylamine.

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