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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738366Generated: October 27, 2026

Hydrochloric Acid → 2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoic acid

https://huagongshe.com/reaction/1738366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
Reactant2-Chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzaldehydeHCID 11809922—
ReactantSodium ChloriteHCID 23668197—
ReactantSodium Phosphate, Monobasic, DihydrateHCID 23673460—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoic acidHCID 15671959—

Reaction Steps

A solution of 2.8 g (18 mmol) of sodium dihydrogen phosphate dihydrate in 28 ml of water was added at 10-15° C. to a solution of 24 g (71 mmol) of 2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzaldehyde in 130 ml of acetonitrile. Then, 6.8 ml of 30% strength aqueous hydrogen peroxide solution and (in the course of one hour) 9.8 g (108 mmol) of sodium chlorite were added in succession. After the mixture had been stirred for a further hour, it was heated to room temperature. After it had been stirred for a further 16 hours, it was acidified using dilute hydrochloric acid. The aqueous solution was then extracted twice using ethyl acetate, whereupon the combined organic phases were washed in succession with concentrated aqueous thiosulfate solution, water and saturated sodium chloride solution, dried over magnesium sulfate and finally concentrated. Yield: 23 g; m.p.: 137-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962694
Source datasetuspto-grants-1999_10
ORD IDord-7b832928780c4aa4812d0e862d3871fa
Source noteuspto-grants-1999_10