{"title":"Solvent-free zinc-mediated Béchamp reduction using mechanochemistry†","authors":"Koji Kubota, Asahi Nagao and Hajime Ito","doi":"10.1039/D4MR00138A","DOIUrl":null,"url":null,"abstract":"<p >In this study, we report the first mechanochemical protocol for highly efficient solvent-free Béchamp reduction using inexpensive Zn metal as a reductant in combination with NH<small><sub>4</sub></small>Cl. This reaction is considerably faster than previous solution-based reactions. Herein, a variety of nitroarenes were chemoselectively reduced to the corresponding primary aromatic amines in good yields within 30 min. Notably, the present solvent-free protocol does not require an organic solvent or air-sensitive and/or expensive reagents, and all synthetic operations can be performed under ambient conditions, greatly enhancing its practical utility. Furthermore, the feasibility of the gram-scale reaction as well as the synthesis of an important intermediate of the muscle relaxant tizanidine were demonstrated.</p>","PeriodicalId":101140,"journal":{"name":"RSC Mechanochemistry","volume":" 3","pages":" 389-393"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/mr/d4mr00138a?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Mechanochemistry","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/mr/d4mr00138a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, we report the first mechanochemical protocol for highly efficient solvent-free Béchamp reduction using inexpensive Zn metal as a reductant in combination with NH4Cl. This reaction is considerably faster than previous solution-based reactions. Herein, a variety of nitroarenes were chemoselectively reduced to the corresponding primary aromatic amines in good yields within 30 min. Notably, the present solvent-free protocol does not require an organic solvent or air-sensitive and/or expensive reagents, and all synthetic operations can be performed under ambient conditions, greatly enhancing its practical utility. Furthermore, the feasibility of the gram-scale reaction as well as the synthesis of an important intermediate of the muscle relaxant tizanidine were demonstrated.