氯氧铋作为醛酮缩合反应的高效非均相催化剂

N. Oanh, Nguyen Vinh Huu, L. Nong
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引用次数: 0

摘要

醛醇反应是现代合成有机化学的基石,其中β-羟基酮是由烯醇或烯酸酯与羰基化合物反应形成的。苯扎拉丙酮是苯扎拉丙酮合酶结构的基本组成部分之一,在构建多种药用上至关重要的苯丁烷类化合物中起着重要作用,如大黄和姜辣素中的抗炎苷林德莱因。非过渡金属材料以其相对稳定、耐空气和湿气、毒性低等显著的化学和物理性质,受到了世界各国研究团体的广泛关注,成为生物硅等有机反应的潜在催化剂。采用溶剂热法合成了BiOCl材料。通过x射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、扫描电镜(SEM)和氮吸附-脱附等温线等现代分析方法确定了材料的结构特征。成功地将BiOCl材料用作苯甲醛与丙酮缩醛反应的催化剂。该反应在温和条件下进行,催化剂用量为10 mol%,碱用量为2等量的Cs2CO3,无副产物,反应时间短,产率高。在120℃下反应24 h,苯甲丙酮的产率达到85%左右。反应后的BiOCl材料可以回收并多次重复使用,催化活性没有明显降低。版权所有©2023作者,BCREC集团出版。这是一篇基于CC BY-SA许可(https://creativecommons.org/licenses/by-sa/4.0)的开放获取文章。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bismuth Oxychloride as an Efficient Heterogeneous Catalyst for Aldol Condensation Reaction between Aldehydes and Ketones
The aldol reaction is a cornerstone of modern synthetic organic chemistry in which the β-hydroxyketone was formed by the reaction of an enol or an enolate and a carbonyl compound. Benzalacetone is one of the fundamental building blocks of benzalacetone synthase structure that play an important role for construction of a variety of medicinally crucial phenylbutanoids, such as anti-inflammatory glucoside lindleyin in rhubarb and gingerol. The non-transition metal material attracted much attention from research groups on the world, such a potential catalyst as BiOCl for organic reaction due to its remarkably chemical and physical properties as relative stability, resistance of air and moisture, low toxicity. The BiOCl material was synthesized by the solvothermal method. The structure features of material were defined by modern analytic methods such as X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FT-IR), Scaning Electron Microscope (SEM), and Nitrogen Adsorption-Desorption Isotherms. The BiOCl material was successfully utilized as a catalyst for the aldol condensation reaction of benzaldehyde and acetone. The reaction was performed in the mild condition with the presence of 10 mol% catalyst and 2 equivalent of Cs2CO3 as base without by-product in very short reaction times and good yields. The benzalacetone product obtained around 85% yield at 120 °C for 24 h. The BiOCl material after reaction was recovered and reused many times without significant reducing of catalytic activity. Copyright © 2023 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 
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