{"title":"苯三甲基三溴化铵对某些半合成和天然酚的溴化作用","authors":"E. V. Buravlev","doi":"10.1007/s11172-024-4490-5","DOIUrl":null,"url":null,"abstract":"<div><p>It was shown that benzyltrimethylammonium tribromide is a convenient reagent for the synthesis of bromo derivatives of 2-isobornylphenols and natural phenolic compounds, <i>viz.</i>, thymol and carvacrol. The use of this reagent allows synthesizing mono- and dihalogenated products bearing the substituents at the <i>ortho</i>- and/or <i>para</i>-positions.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"73 12","pages":"3799 - 3802"},"PeriodicalIF":1.7000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Benzyltrimethylammonium tribromide in bromination of some semisynthetic and natural phenols\",\"authors\":\"E. V. Buravlev\",\"doi\":\"10.1007/s11172-024-4490-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>It was shown that benzyltrimethylammonium tribromide is a convenient reagent for the synthesis of bromo derivatives of 2-isobornylphenols and natural phenolic compounds, <i>viz.</i>, thymol and carvacrol. The use of this reagent allows synthesizing mono- and dihalogenated products bearing the substituents at the <i>ortho</i>- and/or <i>para</i>-positions.</p></div>\",\"PeriodicalId\":756,\"journal\":{\"name\":\"Russian Chemical Bulletin\",\"volume\":\"73 12\",\"pages\":\"3799 - 3802\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Chemical Bulletin\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11172-024-4490-5\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Chemical Bulletin","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11172-024-4490-5","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Benzyltrimethylammonium tribromide in bromination of some semisynthetic and natural phenols
It was shown that benzyltrimethylammonium tribromide is a convenient reagent for the synthesis of bromo derivatives of 2-isobornylphenols and natural phenolic compounds, viz., thymol and carvacrol. The use of this reagent allows synthesizing mono- and dihalogenated products bearing the substituents at the ortho- and/or para-positions.
期刊介绍:
Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections:
General and Inorganic Chemistry;
Physical Chemistry;
Organic Chemistry;
Organometallic Chemistry;
Chemistry of Natural Compounds and Bioorganic Chemistry.