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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399937Generated: November 3, 2026

Pyrazole → 2-Chloro-4-methylsulfonyl-3-(pyrazol-1-yl)benzoic Acid

https://huagongshe.com/reaction/399937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-3-fluoro-4-methylsulfonylbenzoic acidHCID 15451759—
SolventDimethylformamideHCID 6228—
Product2-Chloro-4-methylsulfonyl-3-(pyrazol-1-yl)benzoic AcidHCID 15451767—

Reaction Conditions

Temperature50 °C

Reaction Steps

Pyrazole (210 mg, 3.09 mmol) was added to 190 mg (4.75 mmol) of 60 percent oil dispersed sodium hydride suspended in 7 mL of dry dimethylformamide. After the gas evolution had subsided, 500 mg (1.98 mmol) of 2-chloro-3-fluoro-4-methylsulfonylbenzoic acid was added and the mixture was stirred at 50° C. overnight. The mixture was then concentrated by evaporation under reduced pressure and the residue was partitioned between ethyl acetate and 1N aqueous hydrochloric acid. The aqueous phase was extracted with ethyl acetate. The organic phases were combined and extracted with dilute aqueous sodium bicarbonate solution. The aqueous extract was acidified with 1N aqueous hydrochloric acid and extracted with dichloromethane. The organic extract was concentrated by evaporation under reduced pressure. The crystalline residue obtained was purified by rinsing with ethyl acetate to obtain 540 mg (91 percent of theory) of the title compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05824802
Source datasetuspto-grants-1998_10
ORD IDord-18a733613b2f4c5b8318fa7bdbf90ed9
Source noteuspto-grants-1998_10