铁酸锌作为可重复使用的绿色催化剂合成喹啉衍生物

IF 1.7 4区 化学 Q3 Chemistry
Ganesh Baburao Pund, Sambhaji Tukaram Dhumal, Madhav Janardan Hebade, Mazahar Farooqui, Bhagwansing Shivsing Dobhal
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引用次数: 2

摘要

以双金属环保催化剂ZnFe2O4为催化剂,采用邻苯二胺与取代苯酰溴进行环缩合反应,制备了一种简便的合成喹诺啉的方法。当前方案的辅助优点包括反应时间短,反应条件温和,催化剂可重复使用,环境温度,底物范围广,处理程序简单,收率高,无需色谱分离。同样地,我们观察到,在这些反应条件下,与已知的合成喹诺啉的方法相比,我们很容易实现上述所有的好处。因此,该方法也将为工业规模合成喹诺啉类衍生物提供新的途径。在本方案中,以各种取代的苯酰溴和邻苯二胺为原料,以ZnFe2O4为双金属环保催化剂,在室温下合成了喹啉衍生物。在这里,二甲基甲酰胺被用作溶剂,收率高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Zinc ferrite as reusable and green catalyst for synthesis of quinoxaline derivatives

Zinc ferrite as reusable and green catalyst for synthesis of quinoxaline derivatives

A convenient method for synthesis of quinoxaline has been accomplished by cyclo condensation of substituted phenacyl bromides with o-phenylenediamines in ZnFe2O4 as a bimetallic and eco-friendly catalyst. The auxiliary benefits of the current protocol include short reaction time, mild reaction conditions, reusability of catalyst, ambient temperature, a wide substrate scope, a simple work-up procedure, good yields, and no chromatographic separation. Similarly, it was observed that under these reaction conditions, we had achieved all the above-mentioned benefits easily as compared to already known methods for the synthesis of quinoxalines. Therefore, this methodological approach will generate new pathways to synthesize the derivatives of quinoxalines on the industrial scale too.

Graphical abstract

In the present protocol, the synthesis of quinoxaline derivatives is described using various substituted phenacyl bromides and o-phenylenediamines as starting materials in ZnFe2O4 as a bimetallic and eco-friendly catalyst at room temperature. Here, Dimethylformamide is used as a solvent with high yields.

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来源期刊
Journal of Chemical Sciences
Journal of Chemical Sciences Chemistry-General Chemistry
CiteScore
2.90
自引率
5.90%
发文量
107
审稿时长
12 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
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