{"title":"微波辅助离子液体催化无溶剂条件下1,2-二取代苯并咪唑的合成","authors":"D. Duc, L. Giang","doi":"10.25073/2588-1140/vnunst.5407","DOIUrl":null,"url":null,"abstract":"An efficient method for the synthesis of 1,2-disubstituted benzimidazoles has been developed from 1,2‐diaminobenzenes and aldehydes using 1-butyl-3-methylimidazolium ([Bmim]BF4) as a catalyst under solvent-free conditions. Various products were obtained in good to excellent yields under microwave irradiation. The synthesis features some advantages such as short reaction time, environmentally benign conditions, simple work-up procedure, and high efficiency.","PeriodicalId":23524,"journal":{"name":"VNU Journal of Science: Natural Sciences and Technology","volume":"38 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Microwave-Assisted, Ionic Liquid-Catalyzed Synthesis of 1,2-Disubstituted Benzimidazoles under Solvent-Free Conditions\",\"authors\":\"D. Duc, L. Giang\",\"doi\":\"10.25073/2588-1140/vnunst.5407\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An efficient method for the synthesis of 1,2-disubstituted benzimidazoles has been developed from 1,2‐diaminobenzenes and aldehydes using 1-butyl-3-methylimidazolium ([Bmim]BF4) as a catalyst under solvent-free conditions. Various products were obtained in good to excellent yields under microwave irradiation. The synthesis features some advantages such as short reaction time, environmentally benign conditions, simple work-up procedure, and high efficiency.\",\"PeriodicalId\":23524,\"journal\":{\"name\":\"VNU Journal of Science: Natural Sciences and Technology\",\"volume\":\"38 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-07-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"VNU Journal of Science: Natural Sciences and Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25073/2588-1140/vnunst.5407\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"VNU Journal of Science: Natural Sciences and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25073/2588-1140/vnunst.5407","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Microwave-Assisted, Ionic Liquid-Catalyzed Synthesis of 1,2-Disubstituted Benzimidazoles under Solvent-Free Conditions
An efficient method for the synthesis of 1,2-disubstituted benzimidazoles has been developed from 1,2‐diaminobenzenes and aldehydes using 1-butyl-3-methylimidazolium ([Bmim]BF4) as a catalyst under solvent-free conditions. Various products were obtained in good to excellent yields under microwave irradiation. The synthesis features some advantages such as short reaction time, environmentally benign conditions, simple work-up procedure, and high efficiency.