Synthesis and Nitration of 7-Hydroxy-4-Methyl Coumarin via Pechmann Condensation Using Eco-Friendly Medias

Fadia Al Haj Hussien, Mohammad Keshe, Khaled Alzobar, Joumaa Merza, Ayman Karam
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引用次数: 13

Abstract

A nitro coumarin derivatives has been synthesized via nitration of 7-hydroxy-4-methyl coumarin wich was synthesized via Pechmann condensation resorcinol with a β-ketoester using Amberlyst-15 as a green and efficient catalyst and by caring out the reaction of resorcinol and ethyl acetoacetate (with 1: 1 mol ratio) in the presence of 0.2 g of Amberlyst-15 at 110°C under solvent-free conditions. These nitro coumarin derivatives have biological activity and momentousness in the industrial fields. The purified products were measured the melting points and characterized by spectral methods: FT-IR, 1H-NMR , 13C-NMR.
生态介质下7-羟基-4-甲基香豆素的Pechmann缩合合成及硝化研究
以邻苯二酚和β-酮酯为绿色高效催化剂,在0.2 g邻苯二酚-15的存在下,在110℃无溶剂条件下,间苯二酚与乙酰乙酸乙酯(1:1摩尔比)反应,7-羟基-4-甲基香豆素经硝化反应合成了一种硝基香豆素衍生物。这些硝基香豆素衍生物具有生物活性和重要的工业应用价值。用FT-IR、1H-NMR、13C-NMR对纯化产物进行了熔点测定和表征。
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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