{"title":"Metal-Free Photooxidation of Toluene Derivatives into the Corresponding Carboxylic Acids and Aldehydes by a HBr/NaOCl·5H2O System","authors":"Masayuki Kirihara, Takuma Kawai, Atsuhito Kitajima, Sho Yamahara, Nena Mori, Yoshikazu Kimura","doi":"10.1002/slct.202403692","DOIUrl":null,"url":null,"abstract":"<p>Photobromination of toluene derivatives using blue LED (454 nm) or UV LEDs (365, 385, 395 nm) with aqueous HBr and NaOCl·5H<sub>2</sub>O in trifluoromethyl benzene afforded the corresponding benzoic acids derivatives. The intermediates were (dibromomethyl)benzene derivatives, isolated in a nitrogen atmosphere. The dibromomethyl benzene derivatives afforded the corresponding aldehydes. After the reaction with HBr, the aqueous layer could be recovered and reused.</p>","PeriodicalId":146,"journal":{"name":"ChemistrySelect","volume":"9 43","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2024-11-11","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.202403692","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
Photobromination of toluene derivatives using blue LED (454 nm) or UV LEDs (365, 385, 395 nm) with aqueous HBr and NaOCl·5H2O in trifluoromethyl benzene afforded the corresponding benzoic acids derivatives. The intermediates were (dibromomethyl)benzene derivatives, isolated in a nitrogen atmosphere. The dibromomethyl benzene derivatives afforded the corresponding aldehydes. After the reaction with HBr, the aqueous layer could be recovered and reused.
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.