ZSM-5-SO3H: An Efficient Catalyst for Acylation of Sulfonamides Amines, Alcohols, and Phenols under Solvent-Free Conditions.

ISRN Organic Chemistry Pub Date : 2013-12-08 eCollection Date: 2013-01-01 DOI:10.1155/2013/951749
Ahmad Reza Massah, Roozbeh Javad Kalbasi, Mahdiehsadat Khalifesoltani, Fariba Moshtagh Kordesofla
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引用次数: 5

Abstract

Sulfonamides amines, alcohols, and phenols were efficiently acylated with carboxylic acid anhydrides and chlorides using ZSM-5-SO3H as catalyst under mild and solvent-free conditions. Also, direct esterification of alcohols with carboxylic acids occurred readily in the presence of this catalyst. Different types of amides and esters were obtained in moderate to high yields and purity after a simple workup. No chromatographic separation is needed for isolation of the acylated product. The catalyst was recovered and reused for up to four times without a noticeable decrease in catalytic activity.

ZSM-5-SO3H:无溶剂条件下磺胺类、胺类、醇类和酚类酰化的高效催化剂。
在温和无溶剂条件下,以ZSM-5-SO3H为催化剂,磺胺类、胺类、醇类和酚类与羧酸酸酐和氯化物进行了高效的酰化反应。此外,在这种催化剂的存在下,醇与羧酸的直接酯化反应很容易发生。经过简单的加工,获得了中高收率和纯度的不同类型的酰胺和酯。不需要色谱分离分离的酰化产物。催化剂被回收并重复使用了四次,催化活性没有明显下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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