A Simple and Efficient Two-Step Synthesis of 1,2,3-Triiodoarenes via Consecutive C-H Iodination/ipso-Iododecarboxylation Strategy: A Potential Application towards ortho-Diiodoarenes by Regioselective Metal-Iodine Exchange Reaction

被引:19
作者
Al-Zoubi, Raed M. [1 ]
Al-Mughaid, Hussein [1 ]
McDonald, Robert [2 ]
机构
[1] Jordan Univ Sci & Technol, Dept Chem, Irbid 22110, Jordan
[2] Univ Alberta, Dept Chem, Gunning Lemieux Chem Ctr, Edmonton, AB T6G 2G2, Canada
关键词
RADICAL DECARBOXYLATIVE BROMINATION; ALIPHATIC CARBOXYLIC-ACIDS; STEREOSELECTIVE-SYNTHESIS; HUNSDIECKER REACTION; CONVENIENT SYNTHESIS; AROMATIC IODIDES; IMAGING AGENTS; ALKYL-HALIDES; BENZOIC-ACIDS; HALOGENATION;
D O I
10.1071/CH14386
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A general, robust, and efficient method for the conversion of benzoic acids to 1,2,3-triiodoarenes and 1,2,3-trihaloarenes via a two-step synthesis is reported. Commercially available benzoic acids were used that can allow the reactions to be performed on multi-gram scales with good-to-excellent yields. This report discloses a practical method for the synthesis of 1,2,3-triiodoarenes and 1,2,3-trihaloarenes that is general in scope, scalable, and easy to workup and purify. A potential application of the target compounds as precursors for novel regioselective metal-iodine exchange reaction of 1,2,3-triiodoarenes was also demonstrated. It provided ortho-diiodoaryl derivatives in a high regioselective fashion that are useful intermediates in synthesis and indeed are hard to synthesize by any other means.
引用
收藏
页码:912 / 918
页数:7
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