A General Palladium-Catalyzed Hiyama Cross-Coupling Reaction of Aryl and Heteroaryl Chlorides

被引:34
|
作者
Yuen, On Ying [1 ,2 ,3 ]
So, Chau Ming [1 ,2 ,3 ]
Man, Ho Wing [1 ,2 ]
Kwong, Fuk Yee [1 ,2 ,3 ]
机构
[1] Hong Kong Polytech Univ, State Key Lab Chirosci, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, Hong Kong, Peoples R China
[3] Hong Kong Polytech Univ, Shenzhen Res Inst SZRI, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
aryl chlorides; aryl(alkoxy)silane; cross-coupling reaction; palladium; phosphine ligand; EFFICIENT LIGAND; ORGANOTIN REAGENTS; VINYL CHLORIDES; ORGANIC HALIDES; BOND FORMATION; BROMIDES; SILOXANE; SUZUKI; ARYLTRIALKOXYSILANES; DERIVATIVES;
D O I
10.1002/chem.201600420
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A general palladium-catalyzed Hiyama cross-coupling reaction of aryl and heteroaryl chlorides with aryl and heteroaryl trialkoxysilanes by a Pd(OAc)(2)/L2 catalytic system is presented. A newly developed water addition protocol can dramatically improve the product yields. The conjugation of the Pd/L2 system and the water addition protocol can efficiently catalyze a broad range of electron-rich, -neutral, -deficient, and sterically hindered aryl chlorides and heteroaryl chlorides with excellent yields within three hours and the catalyst loading can be down to 0.05mol% Pd for the first time. Hiyama coupling of heteroaryl chlorides with heteroaryl silanes is also reported for the first time. The reaction can be easily scaled up 200times (100mmol) without any degasification and purification of reactants; this facilitates the practical application in routine synthesis.
引用
收藏
页码:6471 / 6476
页数:6
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