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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096010Generated: October 30, 2026

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

https://huagongshe.com/reaction/2096010

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 under reduced pressure 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 numberUS08449898B2
Source datasetuspto-grants-2013_05
ORD IDord-46d1652ec4044d4ea42e3bd940041b51
Source noteuspto-grants-2013_05