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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644838Generated: October 30, 2026

Hydrochloric Acid → 3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole

https://huagongshe.com/reaction/644838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-HCID 319771—
ReactantBenzene, 1-chloro-2,3-difluoro-5-(trifluoromethyl)-HCID 2736496—
SolventDimethylformamideHCID 6228—
Product3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazoleHCID 1786242833.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

Potassium carbonate (1.66 g, 12 mmol) was added to a solution of 3-hydroxy-5-methylpyrazole (2.45 g, 25.0 mmol) and 3-chloro-4,5-difluorobenzotrifluoride (2.5 g, 25.0 mmol) in DMF (40 ml), and the mixture was stirred under heating at 70° C. for 4 hours. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid (100 ml) and extracted with ethyl acetate (50 ml×3). An organic layer was washed with water, dried over anhydrous magnesium sulfate and filtered to remove a desiccant, and the solvent was distilled off from the filtrate under reduced pressure. The resultant crude product was purified with a silica gel column (ethyl acetate/hexane=1/5), to give a white solid of 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole (2.29 g, yield: 33.8%). mp: 171-174° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.27 (s, 3H), 5.71 (s, 1H), 7.37 (dd, JHF=1.8 and 9.4 Hz, 1H), 7.54 (s, 1H), 8.85-9.55 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-bbe9b8563ab547a88383120e0eba40e2
Source noteuspto-grants-2010_04