Maryam Nabi , Kirti Sharma , Raj S. Wandre , Amol B. Gade
{"title":"温和水性胶束条件下的一锅模拟-贝克曼重排","authors":"Maryam Nabi , Kirti Sharma , Raj S. Wandre , Amol B. Gade","doi":"10.1039/d5gc00958h","DOIUrl":null,"url":null,"abstract":"<div><div>A sustainable and eco-friendly approach to the Beckmann rearrangement has been developed, leveraging nanomicelles to facilitate the reaction in water under mild conditions. This process efficiently transforms functionalized ketones into corresponding amides in a one-pot sequence, achieving high yields of up to 96%. It is more appealing compared to traditional methods, which require significant amounts of organic solvents. The scalability and robustness of this procedure demonstrate its potential for the synthesis of valuable compounds such as paracetamol and ε-caprolactam.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 18","pages":"Pages 5332-5339"},"PeriodicalIF":9.3000,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"One-pot oximation-Beckmann rearrangement under mild, aqueous micellar conditions†\",\"authors\":\"Maryam Nabi , Kirti Sharma , Raj S. Wandre , Amol B. Gade\",\"doi\":\"10.1039/d5gc00958h\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A sustainable and eco-friendly approach to the Beckmann rearrangement has been developed, leveraging nanomicelles to facilitate the reaction in water under mild conditions. This process efficiently transforms functionalized ketones into corresponding amides in a one-pot sequence, achieving high yields of up to 96%. It is more appealing compared to traditional methods, which require significant amounts of organic solvents. The scalability and robustness of this procedure demonstrate its potential for the synthesis of valuable compounds such as paracetamol and ε-caprolactam.</div></div>\",\"PeriodicalId\":78,\"journal\":{\"name\":\"Green Chemistry\",\"volume\":\"27 18\",\"pages\":\"Pages 5332-5339\"},\"PeriodicalIF\":9.3000,\"publicationDate\":\"2025-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1463926225002912\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926225002912","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
One-pot oximation-Beckmann rearrangement under mild, aqueous micellar conditions†
A sustainable and eco-friendly approach to the Beckmann rearrangement has been developed, leveraging nanomicelles to facilitate the reaction in water under mild conditions. This process efficiently transforms functionalized ketones into corresponding amides in a one-pot sequence, achieving high yields of up to 96%. It is more appealing compared to traditional methods, which require significant amounts of organic solvents. The scalability and robustness of this procedure demonstrate its potential for the synthesis of valuable compounds such as paracetamol and ε-caprolactam.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.