{"title":"离子液体1-丁基-3-甲基咪唑溴([Bmim][Br])作为交叉苯甲酸缩合绿色反应的溶剂和催化剂","authors":"Baramee Phungpis, Kanokkan Worawut, Potchanee Keawkumsan","doi":"10.55164/ajstr.v24i2.242509","DOIUrl":null,"url":null,"abstract":"Cross benzoin condensation using room temperature ionic liquids, namely 1-butyl-3-methylimidazolium bromide ([Bmim][Br]), acted as catalyzed and a solvent under NaOH base condition to afford desired cross-benzoin products 4a-i in satistactory yields (60-70%.) Homo-benzoin condensation 5a-d and 6a also were occurred as side reactions in 9-18% yields.","PeriodicalId":426475,"journal":{"name":"ASEAN Journal of Scientific and Technological Reports","volume":"5 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Ionic Liquid 1-Butyl-3-methylimidazolium Bromide ([Bmim][Br]) Acted as Both Solvent and Catalyst for a Green Reaction of Cross Benzoin Condensation\",\"authors\":\"Baramee Phungpis, Kanokkan Worawut, Potchanee Keawkumsan\",\"doi\":\"10.55164/ajstr.v24i2.242509\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Cross benzoin condensation using room temperature ionic liquids, namely 1-butyl-3-methylimidazolium bromide ([Bmim][Br]), acted as catalyzed and a solvent under NaOH base condition to afford desired cross-benzoin products 4a-i in satistactory yields (60-70%.) Homo-benzoin condensation 5a-d and 6a also were occurred as side reactions in 9-18% yields.\",\"PeriodicalId\":426475,\"journal\":{\"name\":\"ASEAN Journal of Scientific and Technological Reports\",\"volume\":\"5 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-08-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ASEAN Journal of Scientific and Technological Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.55164/ajstr.v24i2.242509\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ASEAN Journal of Scientific and Technological Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55164/ajstr.v24i2.242509","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Ionic Liquid 1-Butyl-3-methylimidazolium Bromide ([Bmim][Br]) Acted as Both Solvent and Catalyst for a Green Reaction of Cross Benzoin Condensation
Cross benzoin condensation using room temperature ionic liquids, namely 1-butyl-3-methylimidazolium bromide ([Bmim][Br]), acted as catalyzed and a solvent under NaOH base condition to afford desired cross-benzoin products 4a-i in satistactory yields (60-70%.) Homo-benzoin condensation 5a-d and 6a also were occurred as side reactions in 9-18% yields.