A New Strategy for the Synthesis of Organosilicon Compounds of Cyclopropane Derivatives.

The one-pot reaction of tetra-substituted cyclopropyl benzyl bromide with tris(trimethylsilyl)methyllithium (TsiLi) and carbon disulfide resulted in 3-(4-((((trimethylsilyl)ethynyl)thio)methyl)phenyl)cyclopropane-1,1,2,2-tetracarbonitrile (3) and 3-(4-((trimethylsilyl)methyl)phenyl)cyclopropane-1,2-dicarbonitrile (4) in excellent yield. The reaction in the absence of carbon disulfide yielded 3-(4-(2,2,2-tris(trimethylsilyl)ethyl)phenyl)cyclopropane-1,1,2,2-tetracarbonitrile (5) in excellent yield at 0°C to room temperature. All structures were characterised by IR, 1H NMR, and 13C NMR spectroscopies. The reaction mechanisms are discussed. A new strategy to synthesise new cyclopropane compounds with organosilicon functional groups at different temperatures and under different conditions leads to various new compounds. A discussion about the different reaction mechanisms and obtained products (characterised by IR, 1H NMR, and 13C NMR spectroscopies) is given. [ABSTRACT FROM AUTHOR]