2-芳基-1-羟基-4-甲基-1H-咪唑-5-羧酸乙酯与苄基卤化物的烷基化反应

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC
P. A. Nikitina, I. A. Os’kina, E. B. Nikolaenkova, E. A. Kulikova, V. S. Miroshnikov, V. P. Perevalov, A. Ya. Tikhonov
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引用次数: 0

摘要

摘要 2-芳基-1-羟基-4-甲基-1H-咪唑-5-羧酸乙酯与取代的苄基卤化物进行烷基化反应,可选择性地生成 O-烷氧基衍生物。无环起始化合物通过缩合反应得到 N-烷基化产物(1-烷基咪唑 3-氧化物)。在咪唑环 2 位上存在 2-羟基苯基取代基时,咪唑氮上的羟基取代基会发生选择性单烷基化反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alkylation of Ethyl 2-Aryl-1-hydroxy-4-methyl-1H-imidazole-5-carboxylates with Benzyl Halides

Alkylation of Ethyl 2-Aryl-1-hydroxy-4-methyl-1H-imidazole-5-carboxylates with Benzyl Halides

Abstract

The alkylation of ethyl 2-aryl-1-hydroxy-4-methyl-1H-imidazole-5-carboxylates with substituted benzyl halides resulted in the selective formation of O-alkoxy derivatives. N-Alkylation products (1-alkylimidazole 3-oxides) were obtained by the condensation reaction from acyclic starting compounds. In the presence of the 2-hydroxyphenyl substituent in the 2-position of the imidazole ring, selective monoalkylation involving the hydroxyl substituent on the imidazole nitrogen takes place.

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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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