Accelerating Effect of DMAP on CuI Catalyzed Buchwald-Hartwig C-N Coupling: Mechanistic Insight to the Reaction Pathway

被引:10
|
作者
Roy, Subhasish [1 ]
Dutta, Mintu Maan [1 ]
Sarma, Manas Jyoti [1 ]
Phukan, Prodeep [1 ]
机构
[1] Gauhati Univ, Dept Chem, Gauhati 781014, Assam, India
来源
CHEMISTRYSELECT | 2019年 / 4卷 / 45期
关键词
Amine; Aryl halide; Buchwlad-Hartwig coupling; CuI; DMAP; BARBIER-TYPE ALLYLATION; EFFICIENT COPPER CATALYST; ARYL HALIDES; HIGHLY EFFICIENT; BOND FORMATION; AROMATIC AMINATION; REUSABLE CATALYST; ROOM-TEMPERATURE; AMINO-ACIDS; ARYLATION;
D O I
10.1002/slct.201903896
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient methodology has been developed for C-N cross-coupling reaction between aryl halide and amine using a catalytic system comprised of CuI and N,N-dimethyl amino pyridine (DMAP). Coupling reactions were carried out in DMSO at 120 degrees C in presence of 5 mol% CuI, 20 mol% DMAP and 2.5 equivalent of KOH. Addition of DMAP was found to be beneficial in accelerating the rate of reaction significantly. Both aryl iodides and aryl bromides could be successfully coupled with different primary and secondary amines to furnish the desired cross-coupling product in high yield. A copper complex [Cu(DMAP)(4)I]I made by combining CuI and DMAP was found to produce superior result for the Buchwlad-Hartwig cross coupling reaction. The use of 2 mol% of the copper complex is sufficient to produce high yield of the product.
引用
收藏
页码:13094 / 13098
页数:5
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