879630-45-2Relevant articles and documents
Synthesis and characterization of amine-alkylcyanoboranes
Mills, Wyatt J.,Sutton, Christopher H.,Libby, Eduardo,Todd, Lee J.
, p. 302 - 308 (2008/10/08)
Synthetic methods for the conversion of alkyltrihydroborates to amine-alkylcyanoboranes have been developed. The most efficient of these is cyanation of the alkyltrihydroborates with mercuric cyanide to give the corresponding alkylcyanodihydroborates. These stable salts, when treated with 1 equiv of HCl in diethyl ether, followed by addition of an amine, produce the amine-alkylcyanoboranes (amine = Me3N, py, TMED, quinuclidine; alkyl = methyl, benzyl, sec-butyl, isobutyl) in moderate yield. The new amine-alkylcyanoboranes are thermally, oxidatively, and hydrolytically stable and can be purified by using standard chromatographic methods.