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Two-step Continuous-flow Synthesis of 1,2-dimethyl-3-methylsulfanylbenzene via Diazotization and Methanethiolation
Current Organic Chemistry ( IF 1.7 ) Pub Date : 2024-01-26 , DOI: 10.2174/0113852728277310240103111746
lixia Li 1 , Qi Zhang 1 , Ce Bian 1 , Wei Wei 1 , Wenxuan Sun 1 , Lu Ji 1 , Hande Wang 1 , Chuan Zhou 1 , Ke Wang 1 , Dangsheng Gong 1 , Dongmao Yan 1
Affiliation  

1,2-Dimethyl-3-methylsulfanylbenzene is the key intermediate of topramezone. This work designed a two-step continuous-flow device to synthesize 1,2-dimethyl-3- methylsulfanylbenzene via diazotization and methanethiolation. The results showed that compared with the batch process, the continuous-flow method greatly shortened the residence time to 1 minute, avoided the accumulation of large amounts of diazonium salts to reduce decomposition and increased the product yield to 91.7%. At the same time, the continuous- flow process improved the safety and efficiency of the reactions, saved reaction time and had good prospects for industrial application.

中文翻译:

重氮化和甲硫基化两步连续流合成1,2-二甲基-3-甲硫基苯

1,2-二甲基-3-甲硫基苯是topramezone的关键中间体。本工作设计了一种两步连续流装置,通过重氮化和甲硫基化合成1,2-二甲基-3-甲硫基苯。结果表明,与间歇法相比,连续流法大大缩短了停留时间至1分钟,避免了大量重氮盐的积累,减少了分解,产品收率提高至91.7%。同时,连续流工艺提高了反应的安全性和效率,节省了反应时间,具有良好的工业应用前景。
更新日期:2024-01-26
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