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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499994Generated: October 29, 2026

Sodium Hydroxide → 3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole

https://huagongshe.com/reaction/499994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylateHCID 57548572—
SolventEthanolHCID 702—
Product3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazoleHCID 1786242888.2%

Reaction Steps

To an ethanol (10 mL) solution of methyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylate (0.53 g, 1.5 mmol) was added 5% sodium hydroxide (8 mL), and the mixture was refluxed under heating for 2 hours. After completion of the reaction, the solvent was distilled off the reaction mixture, and then water was added, followed by extraction with ethyl acetate. The organic layers combined were washed with water, and dried over anhydrous magnesium sulfate and the solvent was distilled off. The resultant residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:5) to give a white solid of 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole (0.39 g, yield: 88.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767827B2
Source datasetuspto-grants-2010_08
ORD IDord-168435d52cd24c1d876f2a0a3608e765
Source noteuspto-grants-2010_08