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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710338Generated: November 1, 2026

Hydrochloric Acid → 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1710338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
ReactantEthyl 5-chloro-1-phenyl-1H-pyrazole-4-carboxylateHCID 13608341—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 714712591%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester (Intermediate 1; 7.3 g, 29.1 mmol) in tetrahydrofuran (70 mL) was added a solution of lithium hydroxide in water (7.3 g, 305 mmol) in water (70 mL). Methanol (˜10 mL) was added dropwise to the reaction mixture until only one layer was visible. The reaction mixture was stirred at 70° C. for 1 hour (reaction progress monitored by TLC). The reaction mixture was acidified to pH 3 with 1N hydrochloric acid and washed with dichloromethane (3×200 mL). The organic layer was dried over magnesium sulfate and evaporated to give 5-chloro-1-phenyl-1H-pyrazole-4-carboxylic acid (5.8 g, 91%), which HPLC analysis indicated was 85% pure. This material was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790711B2
Source datasetuspto-grants-2010_09
ORD IDord-779eb53f8c4a4c94b31b981fb1fb4b7d
Source noteuspto-grants-2010_09