{"title":"磷钨酸促进的酰肼与查尔酮缩合反应的研究 Study on the Condensation Reaction of Hydrazide with Benzylideneacetophenone Catalyzed by Phosphotungstic Acid","authors":"吴阳, 邢雪建, 邢刘桩, 侯亚东, 杨敬辉, 惠永海","doi":"10.12677/JOCR.2016.44013","DOIUrl":null,"url":null,"abstract":"本文以杂多酸–磷钨酸为催化剂,对酰肼与查尔酮的缩合反应进行了研究。经过一系列反应条件的筛选,确立了最佳反应条件,并对底物的普适性进行了考察,得到了一系列高产率的酰腙类目标产物,最高产率达到99%。本反应操作简单,条件温和,为查尔酮酰腙合成提供了一种新的方法。 The condensation of hydrazide with benzylideneacetophenone was studied by using phospho-tungstic acid as catalyst. After a series of reaction conditions, the optimal reaction conditions were established, and the universality of the substrate was investigated. A series of acylhydrazones were obtained with the high yields, up to 99%. The reaction was simple and mild, which provided a new method for the synthesis of chalcone hydrazone.","PeriodicalId":16596,"journal":{"name":"Journal of Organic Chemistry Research","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"磷钨酸促进的酰肼与查尔酮缩合反应的研究 Study on the Condensation Reaction of Hydrazide with Benzylideneacetophenone Catalyzed by Phosphotungstic Acid\",\"authors\":\"吴阳, 邢雪建, 邢刘桩, 侯亚东, 杨敬辉, 惠永海\",\"doi\":\"10.12677/JOCR.2016.44013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"本文以杂多酸–磷钨酸为催化剂,对酰肼与查尔酮的缩合反应进行了研究。经过一系列反应条件的筛选,确立了最佳反应条件,并对底物的普适性进行了考察,得到了一系列高产率的酰腙类目标产物,最高产率达到99%。本反应操作简单,条件温和,为查尔酮酰腙合成提供了一种新的方法。 The condensation of hydrazide with benzylideneacetophenone was studied by using phospho-tungstic acid as catalyst. After a series of reaction conditions, the optimal reaction conditions were established, and the universality of the substrate was investigated. A series of acylhydrazones were obtained with the high yields, up to 99%. The reaction was simple and mild, which provided a new method for the synthesis of chalcone hydrazone.\",\"PeriodicalId\":16596,\"journal\":{\"name\":\"Journal of Organic Chemistry Research\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-12-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organic Chemistry Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12677/JOCR.2016.44013\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12677/JOCR.2016.44013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
本文以杂多酸–磷钨酸为催化剂,对酰肼与查尔酮的缩合反应进行了研究。经过一系列反应条件的筛选,确立了最佳反应条件,并对底物的普适性进行了考察,得到了一系列高产率的酰腙类目标产物,最高产率达到99%。本反应操作简单,条件温和,为查尔酮酰腙合成提供了一种新的方法。 The condensation of hydrazide with benzylideneacetophenone was studied by using phospho-tungstic acid as catalyst. After a series of reaction conditions, the optimal reaction conditions were established, and the universality of the substrate was investigated. A series of acylhydrazones were obtained with the high yields, up to 99%. The reaction was simple and mild, which provided a new method for the synthesis of chalcone hydrazone.
磷钨酸促进的酰肼与查尔酮缩合反应的研究 Study on the Condensation Reaction of Hydrazide with Benzylideneacetophenone Catalyzed by Phosphotungstic Acid
本文以杂多酸–磷钨酸为催化剂,对酰肼与查尔酮的缩合反应进行了研究。经过一系列反应条件的筛选,确立了最佳反应条件,并对底物的普适性进行了考察,得到了一系列高产率的酰腙类目标产物,最高产率达到99%。本反应操作简单,条件温和,为查尔酮酰腙合成提供了一种新的方法。 The condensation of hydrazide with benzylideneacetophenone was studied by using phospho-tungstic acid as catalyst. After a series of reaction conditions, the optimal reaction conditions were established, and the universality of the substrate was investigated. A series of acylhydrazones were obtained with the high yields, up to 99%. The reaction was simple and mild, which provided a new method for the synthesis of chalcone hydrazone.