{"title":"PVP-I催化α-(三氟甲基)-苯乙烯与硫醇的羟基硫化:获得三氟甲基叔醇","authors":"Qian-Ding Zeng, Xinxin Yuan, Jian Wang, Hongmiao Yao, Bu-Bing Zeng, Jiangmeng Ren, Wu-Lin Yang","doi":"10.1002/slct.202405351","DOIUrl":null,"url":null,"abstract":"<p>An efficient method for the synthesis of <i>β</i>-hydroxy-<i>β</i>-CF<sub>3</sub>-thioether has been developed, utilizing povidone-iodine (PVP-I) as a recyclable catalyst and air as the oxidant. The reaction proceeded smoothly at room temperature, yielding the desired <i>β</i>-hydroxy-<i>β</i>-CF<sub>3</sub>-thioether in moderate to good yields. This method can be scaled up to gram-scale without losing any reaction efficiency. The catalyst was also recyclable up to 8 repetitions. The reaction mechanism was investigated and plausible reaction pathway was proposed.</p>","PeriodicalId":146,"journal":{"name":"ChemistrySelect","volume":"10 6","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PVP-I Catalyzed Hydroxysulfurization of α-(Trifluoromethyl)-Styrenes with Thiols: Access to Trifluoromethyl Tertiary Alcohol\",\"authors\":\"Qian-Ding Zeng, Xinxin Yuan, Jian Wang, Hongmiao Yao, Bu-Bing Zeng, Jiangmeng Ren, Wu-Lin Yang\",\"doi\":\"10.1002/slct.202405351\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>An efficient method for the synthesis of <i>β</i>-hydroxy-<i>β</i>-CF<sub>3</sub>-thioether has been developed, utilizing povidone-iodine (PVP-I) as a recyclable catalyst and air as the oxidant. The reaction proceeded smoothly at room temperature, yielding the desired <i>β</i>-hydroxy-<i>β</i>-CF<sub>3</sub>-thioether in moderate to good yields. This method can be scaled up to gram-scale without losing any reaction efficiency. The catalyst was also recyclable up to 8 repetitions. The reaction mechanism was investigated and plausible reaction pathway was proposed.</p>\",\"PeriodicalId\":146,\"journal\":{\"name\":\"ChemistrySelect\",\"volume\":\"10 6\",\"pages\":\"\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-02-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemistrySelect\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/slct.202405351\",\"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":"ChemistrySelect","FirstCategoryId":"92","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/slct.202405351","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
PVP-I Catalyzed Hydroxysulfurization of α-(Trifluoromethyl)-Styrenes with Thiols: Access to Trifluoromethyl Tertiary Alcohol
An efficient method for the synthesis of β-hydroxy-β-CF3-thioether has been developed, utilizing povidone-iodine (PVP-I) as a recyclable catalyst and air as the oxidant. The reaction proceeded smoothly at room temperature, yielding the desired β-hydroxy-β-CF3-thioether in moderate to good yields. This method can be scaled up to gram-scale without losing any reaction efficiency. The catalyst was also recyclable up to 8 repetitions. The reaction mechanism was investigated and plausible reaction pathway was proposed.
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.