4.5 Article

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

Journal

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
Volume 14, Issue -, Pages 389-396

Publisher

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.14.27

Keywords

anodic cyclization; diastereoselective fluorination; electrosynthesis; fluorobenzothiophenone; selective fluorination

Funding

  1. Grants-in-Aid for Scientific Research [17H03095] Funding Source: KAKEN

Ask authors/readers for more resources

We herein report that the regioselective anodic fluorination of S-alkyl benzothioate and its derivatives in various aprotic solvents using Et3N center dot nHF (n = 3-5) and Et4NF center dot nHF (n = 3-5) as supporting electrolyte and a fluorine source successfully provided the corresponding alpha-fluorinated products in moderate yields. Dichloromethane containing Et4NF center dot 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available