In a procedure of extreme simplicity and rapidity a mixture of an arom
atic primary amine, copper (I) cyanide and an alkyl nitrite in dimethy
l sulphoxide yielded fair to moderate yields of the corresponding nitr
iles. Side processes observed were reduction (NH2 --> H), nitration (N
H2 --> NO2) and hydroxylation (NH2 --> OH). In the case of polyhaloani
lines halogen dance products could be detected. Copyright (C) 1996 Els
evier Science Ltd