One-pot synthesis of imines from benzyl alcohol and amines on Au/ZrO2 catalyst

被引:20
|
作者
Cui, Wenjing [1 ]
Zhu, Huaiyong [2 ]
Jia, Meilin [3 ]
Ao, Wulan [3 ]
Zhang, Yulin [3 ]
Zhaorigetu, Bao [3 ]
机构
[1] Inner Mongolia Univ Technol, Coll Chem Engn, Hohhot 010051, Peoples R China
[2] Queensland Univ Technol, Sch Chem Phys & Mech Engn, Brisbane, Qld 4001, Australia
[3] Inner Mongolia Normal Univ, Coll Chem & Environm Sci, Inner Mongolia Key Lab Green Catalysis, Hohhot 010022, Peoples R China
基金
中国国家自然科学基金;
关键词
Imines; Catalytic synthesis; Gold nanoparticles; Benzyl alcohol; Amine; N-ALKYLATION; SECONDARY-AMINES; SUPPORTED GOLD; SELECTIVE OXIDATION; AEROBIC OXIDATION; EFFICIENT; NITROARENES; ALDEHYDES; AMINATION;
D O I
10.1007/s11144-013-0576-z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Imines were synthesized from benzyl alcohol and amines by using catalysts of gold nanoparticles supported on ZrO2 (Au/ZrO2). The effects of reaction time, temperature, gold loadings and base were investigated. High yields were achieved under moderate conditions (60 A degrees C) in the presence of KOCH3. For instance, the yield of N-benzylidenebenzylamine produced from benzyl alcohol and benzylamine on 3 wt% Au/ZrO2 is 87 %. The synthesis of imine involves two reaction steps: selective oxidation of benzyl alcohol to benzaldehyde and the coupling reaction of amines with benzaldehyde. In the first step, the base promotes the selective oxidation. The reactions of benzyl alcohol with three different amines, aniline, n-butylamine and benzylamine, were conducted to produce corresponding imines. The results show that the amine with stronger nucleophilicity has better ability to react with benzaldehyde in the second step, resulting in higher yield of the corresponding imine. We proposed a tentative mechanism for the synthesis process.
引用
收藏
页码:551 / 562
页数:12
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