112082-01-6Relevant articles and documents
GENERATION AND REACTIONS OF CARBANIONS FROM DIALKYLAMINO(METHYLTHIO)ACETONITRILES
Jonczyk, Andrzej,Owczarczyk, Zbyslaw,Makosza, Mieczyslaw,Winiarski, Jerzy
, p. 303 - 310 (2007/10/02)
Dialkylamino(methylthio)acetonitriles 1 have been prepared by two independent pathways.The carbanions generated from 1 in various base/solvent systems reacted with alkyl halides or electrophilic alkenes to give unstable products 2 and 5 respectively.These products were transformed into amides 3 or acids 4 and 6.On the other hand, carbanions from 1 with ethyl maleinate or ω-nitrostyrene afforded products of aliphatic vicarious nucleophilic substitution 7, while with 1-nitronaphthalene, the product of aromatic vicarious nucleophilic substitution 8.