Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589295Generated: October 30, 2026

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

https://huagongshe.com/reaction/589295

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 to are added to 30 ml of toluene. A solution of 2.4 g (62 mmol) of sodium hydroxide in 6 ml of water is 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 is stirred at 50° C. for 7 hours. Once the reaction mixture is back to room temperature, the two phases are separated and the organic phase is extracted with 100 ml of water. The combined aqueous phases are acidified to pH 2 with aqueous hydrochloric acid. The resulting white precipitate is filtered, washed twice 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. 1H NMR (400 MHz, DMSO-d6) δ ppm: 3.78 (s, 3H); 7.12 (t, 1H, JHF=53.60 Hz) 13.19 (s, 1H); IR (KBr): 1688 cm−1 (C═O); 2200-3200 cm−1 broad (hydrogen bond).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09232799B2
Source datasetuspto-grants-2016_01
ORD IDord-d996dedd16e644d78e6836f20d42b5d1
Source noteuspto-grants-2016_01