Chem. J. Chinese Universities ›› 2001, Vol. 22 ›› Issue (S1): 89.

• Articles • Previous Articles     Next Articles

Studies on the Reduction of Aromatic Oximes Using Borohydride Exchange Resin-Nickel Boride (cat.)

CHENG Jun-Ran, WEN Jia, LI Yang-Zhou, GUO Xiang-Yun, HUANG Run-Qiu   

  1. State Key Laboratory of Elemento-Organic Chemistry, Institute of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China
  • Received:2001-07-17 Online:2001-12-31 Published:2001-12-31

Abstract:

Aromatic oximes were reduced with borohydride exchange resin (BER)-nickel acetate in methanol as efficient reducing system, the catalyst nickel boride(Ni2B) was formed in situ.The products of reduction of aromatic ketoximes were the corresponding α-substituted benzylamines, and the products of reduction of aromatic aldoximes were symmetric dibenzyl secondary amines, which was different to the result of reference.Their structures were confirmed by 1HNMR,MS and elemental analysis.

Key words: Aromatic aldoximes(ketoximes), Borohydride exchange resin(BER), Nickel boride, Reduction

CLC Number: 

TrendMD: