Sandhya Acharya, Dhiraj K. Jha, Marc Torres, Samantha Chapa, Anshuman Ravi, Rishi Mathew and John C.-G. Zhao
{"title":"Synthesis of aryl esters using carboxylic acids, triarylphosphites, and N-iodosuccinimide†","authors":"Sandhya Acharya, Dhiraj K. Jha, Marc Torres, Samantha Chapa, Anshuman Ravi, Rishi Mathew and John C.-G. Zhao","doi":"10.1039/D4NJ04215H","DOIUrl":null,"url":null,"abstract":"<p >The direct synthesis of aryl esters from carboxylic acids has been achieved by using triarylphosphites and <em>N</em>-iodosuccinimide in chlorobenzene under neutral reaction conditions. This straight-forward green esterification method provides the desired aryl esters in good to high yields (42 to 99% yield) and a wide range of aromatic and aliphatic carboxylic acids can serve as substrates in this esterification reaction. For more acidic acids, the addition of DBU enhances the reaction yields. A radical mechanism, supported by the results of a radical trapping experiment and <small><sup>31</sup></small>P NMR studies, was proposed to explain the reaction outcome.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 4","pages":" 1208-1213"},"PeriodicalIF":2.7000,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04215h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The direct synthesis of aryl esters from carboxylic acids has been achieved by using triarylphosphites and N-iodosuccinimide in chlorobenzene under neutral reaction conditions. This straight-forward green esterification method provides the desired aryl esters in good to high yields (42 to 99% yield) and a wide range of aromatic and aliphatic carboxylic acids can serve as substrates in this esterification reaction. For more acidic acids, the addition of DBU enhances the reaction yields. A radical mechanism, supported by the results of a radical trapping experiment and 31P NMR studies, was proposed to explain the reaction outcome.