Reactions of primary amines with organolithium compounds
HG Richey Jr, WF Erickson
Index: Richey, Herman G.; Erickson, Wayne F. Journal of Organic Chemistry, 1983 , vol. 48, # 23 p. 4349 - 4357
Full Text: HTML
Citation Number: 13
Abstract
Primary amines react under mild conditions with an excess of an organolithium compound to form imines and a-substituted primary amines. Frequently, N-alkylimines that result from the condensation of these products are also isolated. For example, reactions of PhCHzNHz with RLi (R= n-Bu) in refluxing hexane furnish (after hydrolysis) PhCHRNH2, PhRC= O, PhRC= NCHRPh, and R2C= 0. The organic group of the primary amine can be a primary, ...
Related Articles:
[Yamazaki Bulletin of the Chemical Society of Japan, 1990 , vol. 63, # 1 p. 301 - 303]
[Pinter, Aron; Haberhauer, Gebhard; Hyla-Kryspin, Isabella; Grimme, Stefan Chemical Communications, 2007 , # 36 p. 3711 - 3713]
[Medina, Florian; Michon, Christophe; Agbossou-Niedercorn, Francine European Journal of Organic Chemistry, 2012 , # 31 p. 6218 - 6227]
[Solladie, Guy; Saint Clair, Jean-Francois; Philippe, Michel; Semeria, Didier; Maignan, Jean Tetrahedron Asymmetry, 1996 , vol. 7, # 8 p. 2359 - 2364]
[Journal of the Chemical Society, Chemical Communications, , # 16 p. 1607 - 1608]