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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528539Generated: October 26, 2026

Ethyl bromoacetate → ethyl 5-chloro-3-(trifluoromethyl)-1H-pyrazole-1-acetate

https://huagongshe.com/reaction/1528539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant5-chloro-3-(trifluoromethyl)-1H-pyrazoleHCID 178506197—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productethyl 5-chloro-3-(trifluoromethyl)-1H-pyrazole-1-acetateHCID 66016896—

Reaction Steps

To a suspension of 5-chloro-3-(trifluoromethyl)-1H-pyrazole (i.e. the product of Example 10, Step C) (2.1 g, 12.3 mmol) and potassium carbonate (3.6 g, 26.0 mmol) in 20 mL of N,N-dimethylformamide was added ethyl bromoacetate (2.1 mL, 18.8 mmol), and the resulting mixture was stirred at room temperature for 12 h. The resulting mixture was diluted with ethyl acetate, washed with water, and dried (MgSO4). The reaction mixture was concentrated in vacuo and further purified by medium-pressure liquid chromatography using 0-50% of ethyl acetate in hexanes as eluant to give 940 mg of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090604B2
Source datasetuspto-grants-2015_07
ORD IDord-3304b6db463448279e2b037570ef28aa
Source noteuspto-grants-2015_07