苯扎唑IV.1,3-Dihydro-2H-benzimidazol-2-ones 与氯磺酸的反应

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC
Yu. R. Takhirov, D. A. Dushamov, R. Sh. Kuryazov, R. M. Usmonov
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引用次数: 0

摘要

1,3-二氢-2H-苯并咪唑-2-酮在 50-60°C 下与氯磺酸反应,生成 5-氯磺酰基-1,3-二氢-2H-苯并咪唑-2-酮,而不考虑反应物的比例(1:1 至 1:5)。5-氯-1,3-二氢-2H-苯并咪唑-2-酮未能在 50-60°C 下与氯磺酸反应,而在 110-120°C 下得到相应的 5-氯-6-氯磺酰基衍生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Benzazoles: IV. Reaction of 1,3-Dihydro-2H-benzimidazol-2-ones with Chlorosulfonic Acid

Benzazoles: IV. Reaction of 1,3-Dihydro-2H-benzimidazol-2-ones with Chlorosulfonic Acid

1,3-Dihydro-2H-benzimidazol-2-ones reacted with chlorosulfonic acid at 50–60°C to give 5-chloro­sulfonyl-1,3-dihydro-2H-benzimidazol-2-ones regardless of the reactant ratio (1:1 to 1:5). 5-Chloro-1,3-dihy­dro-2H-benzimidazol-2-ones failed to react with chlorosulfonic acid at 50–60°C, and the corresponding 5-chloro-6-chlorosulfonyl derivatives were obtained at 110–120°C.

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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
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