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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411108Generated: November 4, 2026

Hydrogen Peroxide → 5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1411108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactant5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 19754692—
SolventWaterHCID 962—
Product5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acidHCID 1975469349%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a 500 ml flask, 6.0 g (31 mmol) of 5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehyde were added to 30 ml of toluene. A solution of 2.4 g (62 mmol) of sodium hydroxide in 6 ml of water was added to the reaction mixture, followed by 103 ml of a 30% solution of hydrogen peroxide in water, whilst keeping the temperature below 37° C. After the end of the addition, the reaction mixture was stirred at 50° C. for 7 hours. Once the reaction mixture was back to room temperature, the two phases were separated and the organic phase was extracted with 100 ml of water. The combined aqueous phases were acidified to pH 2 with aqueous hydrochloric acid. The resulting white precipitate was filtered, washed two times with 20 ml of water, and dried to yield 3.2 g of 5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921575B2
Source datasetuspto-grants-2014_12
ORD IDord-3e4505d38beb4318991a4feff39ac728
Source noteuspto-grants-2014_12