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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593373Generated: October 26, 2026

Methanol → 4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/593373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
Reactant4-Chloro-1-difluoromethyl-1H-pyrazole-3-carboxylic acid methyl esterHCID 57475883—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-1-(difluoromethyl)-1H-pyrazole-3-carboxylic acidHCID 57475856108.6%

Reaction Steps

A solution of 4-chloro-1-difluoromethyl-1H-pyrazole-3-carboxylic acid methyl ester (540 mg, 2.6 mmol) in tetrahydrofuran (18 ml) was treated at room temperature with a solution of lithium hydroxide (135 mg, 5.6 mmol) in a 1:1-mixture of water and methanol (12 ml). After 1 hour the reaction was complete, and the solvents were evaporated at reduced pressure. The residue was dissolved in water (10 ml) and acidified with hydrochloric acid (2M). Extraction with ethyl acetate, drying of the organic layer over sodium sulphate, and evaporation at reduced pressure yielded a white solid (555 mg) which was triturated with pentane (10 ml). The solid material was filtered, washed with pentane and dried. After drying at reduced pressure the 4-chloro-1-difluoromethyl-1H-pyrazole-3-carboxylic acid was obtained as a white solid (477 mg, 95%); (calculated) C5H3ClF2N2O2 [196.540]; (found) [M'H]−=195.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242943B2
Source datasetuspto-grants-2016_01
ORD IDord-645ac7c264b54906ba68a5c0c7d24142
Source noteuspto-grants-2016_01