Satheeshkumar Rajendran, Nitin Bharat Charbe, Nikhil D. Amnerkar, Arul Murugesan, Saurabh C. Khadse, Sushesh Srivatsa Palakurthi, Sai Raghuveer Chava, Kolandaivel Prabha, Roberto Acevedo
{"title":"Comprehensive Impact of Eaton's Reagent in Organic Synthesis: An Overview","authors":"Satheeshkumar Rajendran, Nitin Bharat Charbe, Nikhil D. Amnerkar, Arul Murugesan, Saurabh C. Khadse, Sushesh Srivatsa Palakurthi, Sai Raghuveer Chava, Kolandaivel Prabha, Roberto Acevedo","doi":"10.1002/slct.202502756","DOIUrl":null,"url":null,"abstract":"<p>Eaton's reagent is a unique mixture of phosphorus pentoxide and methanesulfonic acid and has emerged as a versatile and potent catalyst in modern synthetic chemistry. This review provides a comprehensive overview of Eaton's reagent, detailing its preparation, mechanistic pathways, and diverse applications in organic synthesis. Since its introduction, Eaton's reagent has become invaluable, promoting a wide range of transformations, including Friedel–Crafts reactions, cyclodehydration, Beckmann rearrangement, aminolysis, and multi-component reactions. The reagent's distinct advantages over traditional catalysts, such as higher reactivity, milder reaction conditions, and improved yields, make it particularly effective for synthesizing heterocyclic compounds, pharmaceuticals, natural products, polymers, and advanced materials. Eaton's reagent has also been shown to facilitate solvent-free and eco-friendly synthetic methodologies, aligning with the increasing demand for sustainable chemical processes. This review consolidates recent advancements and applications of Eaton's reagent, underscoring its critical role in advancing synthetic methodologies and providing a foundation for future research to explore innovative reactions, mechanisms, and broader applications in organic synthesis.</p>","PeriodicalId":146,"journal":{"name":"ChemistrySelect","volume":"10 28","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistrySelect","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/slct.202502756","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Eaton's reagent is a unique mixture of phosphorus pentoxide and methanesulfonic acid and has emerged as a versatile and potent catalyst in modern synthetic chemistry. This review provides a comprehensive overview of Eaton's reagent, detailing its preparation, mechanistic pathways, and diverse applications in organic synthesis. Since its introduction, Eaton's reagent has become invaluable, promoting a wide range of transformations, including Friedel–Crafts reactions, cyclodehydration, Beckmann rearrangement, aminolysis, and multi-component reactions. The reagent's distinct advantages over traditional catalysts, such as higher reactivity, milder reaction conditions, and improved yields, make it particularly effective for synthesizing heterocyclic compounds, pharmaceuticals, natural products, polymers, and advanced materials. Eaton's reagent has also been shown to facilitate solvent-free and eco-friendly synthetic methodologies, aligning with the increasing demand for sustainable chemical processes. This review consolidates recent advancements and applications of Eaton's reagent, underscoring its critical role in advancing synthetic methodologies and providing a foundation for future research to explore innovative reactions, mechanisms, and broader applications in organic synthesis.
期刊介绍:
ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.