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The selective electrochemical fluorination of S-alkyl benzothioate and its derivatives

We herein report that the regioselective anodic fluorination of S-alkyl benzothioate and its derivatives in various aprotic solvents using Et(3)N·nHF (n = 3–5) and Et(4)NF·nHF (n = 3–5) as supporting electrolyte and a fluorine source successfully provided the corresponding α-fluorinated products in...

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Detalles Bibliográficos
Autores principales: Kuribayashi, Shunsuke, Kurioka, Tomoyuki, Inagi, Shinsuke, Lu, Ho-Jung, Uang, Biing-Jiun, Fuchigami, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827776/
https://www.ncbi.nlm.nih.gov/pubmed/29520303
http://dx.doi.org/10.3762/bjoc.14.27
Descripción
Sumario:We herein report that the regioselective anodic fluorination of S-alkyl benzothioate and its derivatives in various aprotic solvents using Et(3)N·nHF (n = 3–5) and Et(4)NF·nHF (n = 3–5) as supporting electrolyte and a fluorine source successfully provided the corresponding α-fluorinated products in moderate yields. Dichloromethane containing Et(4)NF·4HF was found to be the most suitable combination as electrolytic solvent and supporting salt as well as fluorine source for the anodic fluorination. The electrochemical fluorination of cyclic benzothioates such as benzothiophenone was also achieved.