A new synthetic route for the preparation of β-acyloxy mercaptans via the addition of thioacids to epoxides

被引：9
|
作者：
Abbasi, Mohammad [1 ]
机构：
[1] Persian Gulf Univ, Coll Agr & Nat Resources, Dept Fisheries & Aquaculture, Bushehr 75169, Iran
来源：
TETRAHEDRON LETTERS | 2012年 / 53卷 / 21期
关键词：
Thioacid; Epoxide; Silica gel; Et3N; beta-Acyloxy mercaptan; THIOLS; INHIBITORS;
D O I：
10.1016/j.tetlet.2012.03.045
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A new synthetic route for the preparation of S-benzylated beta-acyloxy mercaptans starting from the one-pot reaction of thioacids and epoxides using a silica gel/Et3N combined catalyst is described. The thiol functionality in the crude product is then protected via benzylation and the corresponding thioethers are isolated after chromatography. (C) 2012 Published by Elsevier Ltd.
引用
收藏
页码：2608 / 2610
页数：3
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