{"title":"铁酸锌作为可重复使用的绿色催化剂合成喹啉衍生物","authors":"Ganesh Baburao Pund, Sambhaji Tukaram Dhumal, Madhav Janardan Hebade, Mazahar Farooqui, Bhagwansing Shivsing Dobhal","doi":"10.1007/s12039-022-02074-w","DOIUrl":null,"url":null,"abstract":"<div><p>A convenient method for synthesis of quinoxaline has been accomplished by cyclo condensation of substituted phenacyl bromides with <i>o</i>-phenylenediamines in ZnFe<sub>2</sub>O<sub>4</sub> 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.</p><h3>Graphical abstract</h3><p>In the present protocol, the synthesis of quinoxaline derivatives is described using various substituted phenacyl bromides and <i>o</i>-phenylenediamines as starting materials in ZnFe<sub>2</sub>O<sub>4</sub> as a bimetallic and eco-friendly catalyst at room temperature. Here, Dimethylformamide is used as a solvent with high yields.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":50242,"journal":{"name":"Journal of Chemical Sciences","volume":"134 3","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2022-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Zinc ferrite as reusable and green catalyst for synthesis of quinoxaline derivatives\",\"authors\":\"Ganesh Baburao Pund, Sambhaji Tukaram Dhumal, Madhav Janardan Hebade, Mazahar Farooqui, Bhagwansing Shivsing Dobhal\",\"doi\":\"10.1007/s12039-022-02074-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A convenient method for synthesis of quinoxaline has been accomplished by cyclo condensation of substituted phenacyl bromides with <i>o</i>-phenylenediamines in ZnFe<sub>2</sub>O<sub>4</sub> 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.</p><h3>Graphical abstract</h3><p>In the present protocol, the synthesis of quinoxaline derivatives is described using various substituted phenacyl bromides and <i>o</i>-phenylenediamines as starting materials in ZnFe<sub>2</sub>O<sub>4</sub> as a bimetallic and eco-friendly catalyst at room temperature. Here, Dimethylformamide is used as a solvent with high yields.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":50242,\"journal\":{\"name\":\"Journal of Chemical Sciences\",\"volume\":\"134 3\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2022-08-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Sciences\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12039-022-02074-w\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-022-02074-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Chemistry","Score":null,"Total":0}
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.
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.