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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722008Generated: October 29, 2026

Water → 1-(4-Carboxy-3-chlorophenyl)-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/722008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium PermanganateHCID 516875—
Reactant2-Chloro-4-(3-methyl-1H-pyrazol-1-yl)benzoic acidHCID 10847454—
Product1-(4-Carboxy-3-chlorophenyl)-1H-pyrazole-3-carboxylic acidHCID 2188234416%

Reaction Steps

A vigorously stirred solution of 2-chloro-4-(3-methyl-1 H-pyrazol-1-yl)benzoic acid (7.08 g, 30.0 mmol) and 1 N potassium hydroxide (30 mL, 30.0 mmol) in water (200 mL) was heated to between 60–65° C. and treated gradually over ninety minutes with several aliquots of solid potassium permanganate (Total: 49.78 g, 315 mmol, 5.25 equivalents). The mixture was heated for an additional 2.5 hours (4 hours total). After cooling to room temperature, the mixture was filtered and evaporated to a residue. The residue was dissolved in 2 N hydrochloric acid and extracted with ethyl acetate (3×). The combined organic phase was washed with water, dried over anhydrous sodium sulfate, filtered, and the solvent removed in vacuo to yield, after crystallization from a mixture of ethyl acetate-diethyl ether-hexane, the title compound (1.27 g, 4.8 mmol, 16%) as a homogeneous solid, m.p. 260–263° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138393B2
Source datasetuspto-grants-2006_11
ORD IDord-aeea68427383430c858e8417ccf3e86b
Source noteuspto-grants-2006_11