Development of boronic acid catalysts for direct amidation of aromatic carboxylic acids using fluorescence-based screening

被引:1
|
作者
Ryoo, Jeong Yup [1 ]
Han, Min Su [1 ]
机构
[1] Gwangju Inst Sci & Technol GIST, Dept Chem, 123 Cheomdangwagi Ro, Gwangju 61005, South Korea
基金
新加坡国家研究基金会;
关键词
DIRECT AMIDE FORMATION; COUPLING REAGENT; AMINES; TRANSAMIDATION; HYDROCHLORIDE; OPTIMIZATION; AMINATION; EFFICIENT; PRESSURE; ASSAY;
D O I
10.1039/d4ob00576g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Direct amidation of carboxylic acids with amines holds significant importance; therefore, catalytic processes involving boronic acids have undergone extensive investigation. However, studies focused on the amidation of aromatic carboxylic acids remain limited. In this study, we introduce a fluorescence-based screening methodology employing an anthracene derivative probe, facilitating the rapid evaluation of various amidation catalysts. Using this approach, boronic acids were evaluated for their catalytic potential. Our findings reveal that 2-hydroxyphenylboronic acid (C7), previously deemed inefficient for aliphatic acids, effectively catalyzes the amidation of aromatic acids. The catalysts identified through this method consistently achieved high yields, reaching up to 98% across a broad spectrum of substrates. Boronic acid catalysts for direct amidation were rapidly evaluated using fluorescence-based screening, achieving yields up to 98% with the most effective catalyst among them.
引用
收藏
页码:6103 / 6107
页数:5
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