REDUCTIVE ELECTROCHEMICAL SILYLATION OF UNSATURATED NITROGEN FUNCTIONALITIES - A SIMPLE AND EFFICIENT SYNTHESIS OF PRECURSORS OF BIS(TRIMETHYLSILYL)METHYLAMINE

Citation
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
Citations number
38
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
13
Issue
9
Year of publication
1994
Pages
3711 - 3714
Database
ISI
SICI code
0276-7333(1994)13:9<3711:RESOUN>2.0.ZU;2-8
Abstract
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.