Electrochemical C-H trifluoromethylation of 4-phenylthiazol-2-amines
Yesilyurt, Isa, Dagalan, Ziya, Anil, Baris, Kocak, Ramazan, Bayrakceken Nisanci, Fatma, Nisanci, Bilal
Herein, we report a new methodology for the electrochemical oxidative C-H trifluoromethylation of 4-phenylthiazol-2-amines in an undivided cell using a glassy carbon electrode (GCE) and sodium trifluoromethanesulfinate (CF3SO2Na; Langlois' reagent) as the CF3 radical source. Using this tert-butyl hydroperoxide (TBHP)-mediated and transition metal-free effective approach, trifluo-romethylated 4-phenylthiazol-2-amines were synthesized in high yields (up to 97%).
- Journal
- ORGANIC & BIOMOLECULAR CHEMISTRY
- Year
- 2026
- Volume
- 24
- Issue
- 7
- Pages
- 1434-1439
- ISSN
- 1477-0520
- eISSN
- 1477-0539
- DOI
- 10.1039/d5ob01958c
- WoS UID
- WOS:001675299400001