Synthesis of Aryl Ethers from Aromatic Carboxylic Acids

被引:8
|
作者
Bhadra, Sukalyan [1 ]
Dzik, Wojciech I. [1 ]
Goossen, Lukas J. [1 ]
机构
[1] Tech Univ Kaiserslautern, Dept Chem, D-67663 Kaiserslautern, Germany
来源
SYNTHESIS-STUTTGART | 2013年 / 45卷 / 17期
关键词
aryl ethers; C-C activation; C-H activation; C-O bond formation; decarboxylative coupling; HYDROXYLATION;
D O I
10.1055/s-0033-1339470
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A silver/copper bimetallic catalyst system promotes the decarboxylative Chan-Evans-Lam alkoxylation of ortho-substituted aromatic carboxylate salts with tetraalkyl orthosilicates or triaryl borates. Non-ortho-substituted carboxylates are alkoxylated via an ortho-C-H-alkoxylation with concomitant cleavage of the carboxylate directing group via protodecarboxylation. This way, meta-substituted carboxylates are converted into para-substituted alkoxyarenes and vice versa. The combined processes provide a convenient synthetic entry to the important class of aromatic ethers from widely available carboxylic acids.
引用
收藏
页码:2387 / 2390
页数:4
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