Synthesis of aryl esters using carboxylic acids, triarylphosphites, and N-iodosuccinimide†

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Sandhya Acharya, Dhiraj K. Jha, Marc Torres, Samantha Chapa, Anshuman Ravi, Rishi Mathew and John C.-G. Zhao
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引用次数: 0

Abstract

The direct synthesis of aryl esters from carboxylic acids has been achieved by using triarylphosphites and N-iodosuccinimide in chlorobenzene under neutral reaction conditions. This straight-forward green esterification method provides the desired aryl esters in good to high yields (42 to 99% yield) and a wide range of aromatic and aliphatic carboxylic acids can serve as substrates in this esterification reaction. For more acidic acids, the addition of DBU enhances the reaction yields. A radical mechanism, supported by the results of a radical trapping experiment and 31P NMR studies, was proposed to explain the reaction outcome.

Abstract Image

羧酸、三芳基亚磷酸酯和n -碘丁二酰亚胺†合成芳基酯
以三芳基亚磷酸酯和n -碘丁二酰亚胺为原料,在中性条件下以氯苯为原料,由羧酸直接合成芳基酯。这种直接的绿色酯化方法提供了所需的芳基酯,收率高(42 - 99%),各种芳香族和脂肪族羧酸可以作为酯化反应的底物。对于酸性较强的酸,加入DBU可提高反应收率。通过自由基捕获实验和31P核磁共振研究,提出了一种自由基机制来解释反应结果。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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