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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238674Generated: October 26, 2026

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

https://huagongshe.com/reaction/238674

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 numberUS08642634B2
Source datasetuspto-grants-2014_02
ORD IDord-be079ffc1c7142658e3b6a85428947e1
Source noteuspto-grants-2014_02