Efficient and recyclable Cu2(BPDC)2(DABCO)-catalyzed direct amination of activated sp3 C-H bonds by N-H heterocycles

被引:24
|
作者
Thanh Truong [1 ]
Nguyen, Khoa D. [1 ]
Doan, Son H. [1 ]
Phan, Nam T. S. [1 ]
机构
[1] HCMC Univ Technol, VNU HCM, Dept Chem Engn, 268 Ly Thuong Kiet,Dist 10, Ho Chi Minh City, Vietnam
关键词
Metal-organic framework; Cross-coupling; Azoles; Amides; C-N bond activation; Heterogeneous catalyst; METAL-ORGANIC FRAMEWORKS; HETEROGENEOUS CATALYST; COUPLING REACTIONS; ARYLBORONIC ACIDS; LIGAND-FREE; PALLADIUM; CU-2(BPDC)(2)(BPY); ALKYLATION; ARYLATION; AMINES;
D O I
10.1016/j.apcata.2015.10.042
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
A metal-organic framework Cu-2(BPDC)(2)(DABCO) was successfully synthesized and employed as an efficient heterogeneous catalyst for the direct C-N cross-coupling reaction via sp(3) C-N bond activation between N-H heterocycles and amides. Kinetic investigation was thoroughly conducted. The optimal conditions involve the use of Cu-2(BPDC)(2)(DABCO) catalyst (3%), di-tert-butyl peroxide oxidant (2 equivalents) in chlorobenzene solvent at 120 degrees C in 2 h. The Cu-2(BPDC)(2)(DABCO) offered higher catalytic activity than that of other Cu-MOFs such as Cu-2(BPDC)(2)(BPY), Cu-3(BTC)(2) and Cu-2(BDC)(2)(DABCO), and that of several common copper salts such as CuCl, CuBr, CuI, Cu(NO3)(2), and CuSO4. To investigate the mechanism, catalyst poisoning experiments and reactions with added radical scavengers were conducted. Furthermore, the catalyst could be recovered and reused several times without much decline in the reaction yield. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 33
页数:7
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