Cu-Mediated Direct Aryl CH Halogenation: a Strategy to Control Mono- and Di-Selectivity
作者:Zhi-Jun Du、Lian-Xun Gao、Ying-Jie Lin、Fu-She Han
DOI:10.1002/cctc.201300734
日期:2014.1
A protocol for the copper‐mediated directarylCHhalogenation is presented. Highly selective mono‐ and di‐halogenations are achieved by using acyl hypohalites, generated in situ from the readily available carboxylic acid and N‐halosuccinimides (NXS; X=Br and Cl) as powerful halogenating reagents. The correct choice of carboxylic acid additives and solvents is essential for both high yield and selectivity
提出了铜介导的直接芳基CH卤化的方案。通过使用酰基次卤酸盐来实现高度选择性的单卤化和二卤化,酰基次卤酸盐是由现成的羧酸和N-卤代琥珀酰亚胺(NXS; X = Br和Cl)原位生成的,作为强力卤化试剂。正确选择羧酸添加剂和溶剂对于高收率和选择性都至关重要。因此,使用廉价的铜催化剂和从容易负担得起且易于处理的羧酸和NXS(X = Br和Cl)原位生成酰基次卤酸盐卤化试剂的新策略为实际应用提供了优势。
Cu-catalyzed direct ortho-chlorination/-oxygenation of aryls: Switching of oxidant, control the diversity of products
Highly regioselective copper catalyzed ortho-chlorination of aryl pyridines was achieved with TBHP as oxidant and 1,2-dichloroethane as chlorinating agent for the first time. Switching the oxidant from TBHP to benzoylperoxide under identical reaction conditions effects ortho-oxygenation.
AbstractA chemoselective, palladium‐catalyzed, ligand‐directed ortho‐CH chlorination and acylation process has been developed, exhibiting high regioselectivity for 2‐arylpyridines bearing a meta‐substituent. Worthy of note is the fact that arylmethyl chlorides as new, readily available, and inexpensive reagents can selectively be utilized as chlorine or acyl sources.magnified image