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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375653Generated: October 28, 2026

Methanol → 4-(4-Fluoro-phenyl)-3-(4-methanesulfonyl-phenyl)-5-trifluoromethyl-1H-pyrazole

https://huagongshe.com/reaction/375653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-(4-fluorophenyl)-3-[4-(methylthio)phenyl]-5-(trifluoromethyl)-1H-pyrazoleHCID 15380221—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
Product4-(4-Fluoro-phenyl)-3-(4-methanesulfonyl-phenyl)-5-trifluoromethyl-1H-pyrazoleHCID 1538022291%

Reaction Steps

To a solution of the pyrazole from Step 2 (4.0 g, 11.4 mmol) in 150 mL methanol was added a solution of Oxone® (14.0 g, 22.7 mmol) in 50 mL water. After 1 hour the solids were filtered off, washed with ethyl acetate and the filtrate concentrated in vacuo. This mixture was partitioned between ethyl acetate and water, and the organic layer washed with brine, dried over MgSO4 and reconcentrated in vacuo. Recrystallization from chloroform gave 4-(4-fluorophenyl)-3-[4-(methylsulfonyl)phenyl]-5-(trifluoromethyl)-1H-pyrazole (3.98 g, 91%) as a pale yellow solid: mp 219°-220° C. Elemental analysis for C17H12N2F4SO2Calc'd.: C, 53.12, H, 3.15, N, 7.29, S, 8.34. Found: C, 52.85, H, 3.12, N, 7.21, S, 8.61

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486534
Source datasetuspto-grants-1996_01
ORD IDord-8aa20b5e63724886b8c425bcc35f595d
Source noteuspto-grants-1996_01