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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644842Generated: October 30, 2026

Hydrochloric Acid → 3-(3-Chloro-5-trifluoromethylpyridin-2-yloxy)-5-methylpyrazole

https://huagongshe.com/reaction/644842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
Reactant3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-HCID 319771—
SolventDimethylformamideHCID 6228—
Product3-(3-Chloro-5-trifluoromethylpyridin-2-yloxy)-5-methylpyrazoleHCID 1786245776%

Reaction Conditions

Temperature60 °C

Reaction Steps

Potassium carbonate (7.60 g, 55.0 mmol) was added to a solution of 3-hydroxy-5-methylpyrazole (4.90 g, 50.0 mmol) and 2,3-dichloro-5-trifluoromethylpyridine (10.8 g, 50.0 mmol) in DMF (50 ml) at room temperature, and the mixture was stirred under heating at 60° 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 (30 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=1/2), to give a white solid of 3-(3-chloro-5-trifluoromethylpyridin-2-yloxy)-5-methylpyrazole (10.5 g, yield: 76.0%). mp: 93-95° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.32 (s, 3H), 5.90 (s, 1H), 7.98 (d, J=2.0 Hz, 1H), 8.33 (m, 1H), 10.80-11.60 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-e41bc377a4604567a4756ce158f3ef90
Source noteuspto-grants-2010_04