The Reaction of Grignard Reagents with Bunte Salts: A Thiol-Free Synthesis of Sulfides

被引:138
作者
Reeves, Jonathan T. [1 ]
Camara, Kaddy [1 ]
Han, Zhengxu S. [1 ]
Xu, Yibo [1 ]
Lee, Heewon [1 ]
Busacca, Carl A. [1 ]
Senanayake, Chris H. [1 ]
机构
[1] Boehringer Ingelheim Pharmaceut Inc, Ridgefield, CT 06877 USA
关键词
SULFUR BOND FORMATION; CATALYZED SYNTHESIS; AQUEOUS-MEDIA; ARYL; TRISULPHIDES; ACETYLENES; CHEMISTRY; INDIUM; ACID;
D O I
10.1021/ol500067f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
S-Alkyl, S-aryl, and S-vinyl thiosulfate sodium salts (Bunte salts) react with Grignard reagents to give sulfides in good yields. The S-alkyl Bunte salts are prepared from odorless sodium thiosulfate by an S(N)2 reaction with alkyl halides. A Cu-catalyzed coupling of sodium thiosulfate with aryl and vinyl halides was developed to access S-aryl and S-vinyl Bunte salts. The reaction is amenable to a broad structural array of Bunte salts and Grignard reagents. Importantly, this route to sulfides avoids the use of malodorous thiol starting materials or byproducts.
引用
收藏
页码:1196 / 1199
页数:4
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