硫脲/NCBSI/HCl 系统:通过可回收的 N-氯-N-(苯磺酰基)苯磺酰胺 (NCBSI) 将烷基卤伸缩为烷基磺酰氯

IF 2 Q2 CHEMISTRY, ORGANIC
SynOpen Pub Date : 2024-07-16 DOI:10.1055/a-2360-9229
Shweta Gaikwad, G. Chaturbhuj
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引用次数: 0

摘要

本文介绍了一种便捷高效的方法,通过 N-氯-N-(苯磺酰基)苯磺酰胺(NCBSI)介导的从烷基氯化物中获得的 S-烷基异硫鎓盐的氧化氯磺化反应,合成多种烷基磺酰氯。通过使用廉价的硫脲轻松生成 S-烷基异硫鎓盐,以烷基卤化物为原料合成结构多样的烷基磺酰氯,中等至优良收率可达 98%。温和的反应条件和广泛的底物范围使该方法有利于烷基磺酰氯的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Thiourea/NCBSI/HCl System: Telescoping alkyl halide to alkyl sulfonyl chloride by recyclable N-chloro-N-(phenylsulfonyl)benzene sulfonamide (NCBSI)

Thiourea/NCBSI/HCl System: Telescoping alkyl halide to alkyl sulfonyl chloride by recyclable N-chloro-N-(phenylsulfonyl)benzene sulfonamide (NCBSI)
A convenient and efficient method to synthesize diverse alkyl sulfonyl chlorides through N-chloro-N-(phenylsulfonyl)benzene sulfonamide (NCBSI)-mediated oxidative chlorosulfonation of S-alkyl isothiouronium salts obtained from alkyl chlorides is presented. Synthesizing structurally diverse alkyl sulfonyl chloride in moderate to excellent yields up to 98% from alkyl halide via easy formation of S-alkyl isothiouronium salts using inexpensive thiourea. The mild reaction conditions and broad substrate scope make this method beneficial and advantageous to alkylsulfonyl chloride syntheses.
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来源期刊
SynOpen
SynOpen CHEMISTRY, ORGANIC-
CiteScore
2.30
自引率
4.00%
发文量
35
审稿时长
6 weeks
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