REDUCTIVE ELECTROCHEMICAL SILYLATION OF UNSATURATED NITROGEN FUNCTIONALITIES - A SIMPLE AND EFFICIENT SYNTHESIS OF PRECURSORS OF BIS(TRIMETHYLSILYL)METHYLAMINE
S. Grelier et al., REDUCTIVE ELECTROCHEMICAL SILYLATION OF UNSATURATED NITROGEN FUNCTIONALITIES - A SIMPLE AND EFFICIENT SYNTHESIS OF PRECURSORS OF BIS(TRIMETHYLSILYL)METHYLAMINE, Organometallics, 13(9), 1994, pp. 3711-3714
Synthesis of the title compound, 1, via the electroreductive silylatio
n of a series of unsaturated nitrogen derivatives, i.e., trialkylsilyl
cyanides, dimethylcyanamide, tert-butyl isocyanide bis(trimethylsilyl
)carbodiimide, and trimethylsilyl isocyanate, is described in this pap
er. This process involves the use of an undivided cell, a sacrificial
anode, and a constant current density. It gives yields comparable with
those obtained in the previously described chemical route and appears
to be safer and more economical.