{"title":"以苯和水(绿色化学的概念)为溶剂合成迪希夫碱的比较研究","authors":"G. Chawla, Muhamad Thufail","doi":"10.18231/j.ijpca.2020.007","DOIUrl":null,"url":null,"abstract":"Di-Schiff’s bases are normally synthesized from aldehyde and diamine using organic solvents under conditions that remove water azeotropically. Here is a report for the preparation of di-Schiff’s base using both the conventional method and pure water without a catalyst and results were compared. It was observed that yields are better and reaction time is comparatively less when water is used as a solvent.\n\nKeywords: Benzene, Water, Green chemistry.","PeriodicalId":14317,"journal":{"name":"International Journal of Pharmaceutical Chemistry","volume":"82 1","pages":"51-53"},"PeriodicalIF":0.0000,"publicationDate":"2020-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Syntheses of di-Schiff’s bases: A comparative study using benzene and water (concept of green chemistry) as solvents\",\"authors\":\"G. Chawla, Muhamad Thufail\",\"doi\":\"10.18231/j.ijpca.2020.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Di-Schiff’s bases are normally synthesized from aldehyde and diamine using organic solvents under conditions that remove water azeotropically. Here is a report for the preparation of di-Schiff’s base using both the conventional method and pure water without a catalyst and results were compared. It was observed that yields are better and reaction time is comparatively less when water is used as a solvent.\\n\\nKeywords: Benzene, Water, Green chemistry.\",\"PeriodicalId\":14317,\"journal\":{\"name\":\"International Journal of Pharmaceutical Chemistry\",\"volume\":\"82 1\",\"pages\":\"51-53\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Pharmaceutical Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18231/j.ijpca.2020.007\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Pharmaceutical Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18231/j.ijpca.2020.007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Syntheses of di-Schiff’s bases: A comparative study using benzene and water (concept of green chemistry) as solvents
Di-Schiff’s bases are normally synthesized from aldehyde and diamine using organic solvents under conditions that remove water azeotropically. Here is a report for the preparation of di-Schiff’s base using both the conventional method and pure water without a catalyst and results were compared. It was observed that yields are better and reaction time is comparatively less when water is used as a solvent.
Keywords: Benzene, Water, Green chemistry.
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