Cu-catalyzed Goldberg and Ullmann reactions of aryl halides using chelating N- and O-based ligands

被引:52
作者
Altman, Ryan A. [1 ]
Buchwald, Stephen L. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
关键词
D O I
10.1038/nprot.2007.364
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The following protocol can be applied in the selective cross-coupling reaction of an amine with an aryl iodide or bromide using a copper (Cu)-based catalyst to provide the corresponding N-aryl amine. The general procedure described in this text includes a detailed description of an appropriate reaction setup, two methods for assaying the crude reaction mixture (gas chromatography and thin layer chromatography) and a procedure for the isolation, purification and characterization of the anticipated product. Manipulation of the reagents can be done in the air, without the use of a glovebox; however, the cross-coupling reactions must be performed in a sealed reactor under an inert atmosphere. Three C-N bond-forming reactions are included in the protocol as representative examples of this procedure. Although the reactions can proceed in <1 h, the protocols, including workup, generally take 6-30 h to complete.
引用
收藏
页码:2474 / 2479
页数:6
相关论文
共 22 条
[21]   Total synthesis of reblastatin [J].
Wrona, IE ;
Gabarda, AE ;
Evano, G ;
Panek, JS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (43) :15026-15027
[22]   Copper-catalyzed domino halide exchange-cyanation of aryl bromides [J].
Zanon, J ;
Klapars, A ;
Buchwald, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (10) :2890-2891