{"title":"Polynaphthoquinone mediated metal-free direct <i>N</i>-alkylation of (hetero)aryl amines using alcohols.","authors":"Uttam Kumar Panigrahi, Vengadesh Kumara Mangalam Ramakrishnan","doi":"10.1039/d5ob00163c","DOIUrl":null,"url":null,"abstract":"<p><p>Herein, we present polynaphthoquinone as an effective metal-free catalyst for the direct <i>N</i>-alkylation of aryl and heteroaryl amines using alcohols. Our experiments reveal that the optimal reaction conditions consist of 1.0 mmol of alcohol, 1.5 mmol of aniline, 0.8 equivalents of <i>t</i>-BuOK, and 30 wt% polynaphthoquinone catalyst in toluene at 135 °C under an inert atmosphere for 24 hours. Control experiments confirm that without a catalyst or base, the reaction fails to progress. Additionally, the reused catalyst in subsequent reactions yields good to excellent results. This methodology has also been extended to the dehydrogenative synthesis of quinolines and indoles.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5ob00163c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Herein, we present polynaphthoquinone as an effective metal-free catalyst for the direct N-alkylation of aryl and heteroaryl amines using alcohols. Our experiments reveal that the optimal reaction conditions consist of 1.0 mmol of alcohol, 1.5 mmol of aniline, 0.8 equivalents of t-BuOK, and 30 wt% polynaphthoquinone catalyst in toluene at 135 °C under an inert atmosphere for 24 hours. Control experiments confirm that without a catalyst or base, the reaction fails to progress. Additionally, the reused catalyst in subsequent reactions yields good to excellent results. This methodology has also been extended to the dehydrogenative synthesis of quinolines and indoles.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.