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无催化剂和添加剂条件下氟化乙酸对吲哚的 Friedel-Crafts 氟乙酰化反应合成氟甲基吲哚-3-基酮。

Friedel-Crafts Fluoroacetylation of Indoles with Fluorinated Acetic Acids for the Synthesis of Fluoromethyl Indol-3-yl Ketones under Catalyst- and Additive-Free Conditions.

机构信息

Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, Department of Chemistry & Materials Science, Northwest University , Xi'an 710127, People's Republic of China.

出版信息

J Org Chem. 2016 May 20;81(10):4226-34. doi: 10.1021/acs.joc.6b00580. Epub 2016 May 4.

Abstract

A simple and efficient protocol for the fluoroacetylation of indoles is reported. The reaction uses fluorinated acetic acids as the fluoroacetylation reagents to synthesize diverse fluoromethyl indol-3-yl ketones in good yields under catalyst- and additive-free conditions. In addition, the only byproduct is water in this transformation. The synthetic utility of this reaction was also demonstrated by the concise synthesis of α-(trifluoromethyl)(indol-3-yl)methanol and indole-3-carboxylic acid.

摘要

报道了一种吲哚氟乙酰化的简单高效方法。该反应以氟化乙酸作为氟乙酰化试剂,在无催化剂和添加剂的条件下,以良好的收率合成了多种氟甲基吲哚-3-基酮。此外,该转化的唯一副产物是水。该反应的合成实用性还通过α-(三氟甲基)(吲哚-3-基)甲醇和吲哚-3-羧酸的简洁合发展现出来。

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