THIELE ACETYLATION OF QUINONES .2. P-BENZOQUINONES WITH HALOGEN SUBSTITUENTS

被引：15

作者：

BLATCHLY, JM

MCOMIE, JFW

SEARLE, JB

机构：

[1] Charterhouse, Godalming, Surrey

[2] School of Chemistry, The University

来源：

JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC | 1969年 / 10期

关键词：

D O I：

10.1039/j39690001350

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Thiele acetylation of all mono-, di-, and tri-bromo-p-benzoquinones, and of iodo- and 2,6-di-iodo-p-benzoquinone is described. Contrary to a previous report, 2,6-dichloro-p-benzoquinone readily undergoes Thiele acetylation. The assignments of orientation of some previously reported dibromotrimethoxy- benzenes have been shown to be erroneous.

引用

页码：1350 / &