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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571843Generated: October 31, 2026

Methanol → 1-[3-(Difluoromethoxy)phenyl]-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/571843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantEthyl 1-[3-(difluoromethoxy)phenyl]-1H-pyrazole-4-carboxylateHCID 71086782—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
Product1-[3-(Difluoromethoxy)phenyl]-1H-pyrazole-4-carboxylic acidHCID 7108673778%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl 1-(3-(difluoromethoxy)phenyl)-1H-pyrazole-4-carboxylate (5 g, 17.7 mmol) in a mixture of THF (100 ml), methanol (50 ml) and water (50 ml) lithium hydroxide hydrate (2.23 g, 53.1 mmol) was added. The solution was heated to 80° C. for 2 h. Most of the organic solvent was removed under reduced pressure. Sodium bicarbonate solution was added and the organic layer was separated. The aqueous layer was made acidic by addition of 25% aq. hydrochloric acid (until acidic pH) and the mixture was extracted two times with ethyl acetate. The organic layers were combined, dried (MgSO4) and evaporated to yield a solid. The solid was stirred in a mixture of heptane and ethyl acetate for 2 h, filtered off and dried to yield 1-(3-(difluoromethoxy)phenyl)-1H-pyrazole-4-carboxylic acid as an off-white solid (3.5 g, 78%) which was used for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-eed8a6ed67854b86a8a8675c854a21b9
Source noteuspto-grants-2015_05