High-pressure alkylation of bis (benzylidene) phenylenediamines

NE Agafonov, AV Dudin, AA Preobrazhenskii…

Index: Agafonov; Dudin; Preobrazhenskii; Zhulin Russian Chemical Bulletin, 2003 , vol. 52, # 1 p. 273 - 275

Full Text: HTML

Citation Number: 2

Abstract

Abstract The reactions of alkyl chlorides with bisanils (obtained from o-, m-, and p- phenylenediamines) under high pressure (10 kbar) were studied. Depending on the structure of the starting diamines and the solvent nature, hydrolysis of the reaction mixtures gave pure N-monoalkyl-or N, N"-dialkylphenylenediamines in high yields. The effect of the phase transition of the solvent on the direction of alkylation is discussed.

Related Articles:

Trifunctional N, N, O-terdentate amido/pyridyl carboxylate ligated Pd (II) complexes for Heck and Suzuki reactions

[Li, Fuwei; Hor, T. S. Andy Advanced Synthesis and Catalysis, 2008 , vol. 350, # 14-15 p. 2391 - 2400]

More Articles...