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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710614Generated: November 2, 2026

Ethyl bromoacetate → (4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acid

https://huagongshe.com/reaction/710614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazoleHCID 1206965—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acidHCID 187685384.1%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of 4-chloro-5-methyl-3-(trifluoromethyl)pyrazole (15 g, 81.3 mmol) in DMF (82 mL) was added ethyl 2-bromoacetate (13.6 g, 81.3 mmol) and potassium carbonate (12.4 g, 89.4 mmol). The mixture was heated at 55° C. for 10 hours with stirring. After cooling to room temperature, the reaction mixture was diluted with water (100 mL) and extracted with ethyl acetate (3×150 mL). The combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (SiO2, 0-30% ethyl acetate in hexanes) to afford the desired product (18.5 g, 68.4 mmol, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181241B2
Source datasetuspto-grants-2015_11
ORD IDord-f4dba391d020462b9fe73839d26908f6
Source noteuspto-grants-2015_11