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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043745Generated: October 29, 2026

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

https://huagongshe.com/reaction/2043745

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 6601689629.8%

Reaction Steps

A suspension of 5-chloro-3-trifluoromethyl-1H-pyrazole (2.1 g, 12.3 mmol) (i.e. the product of Example 13, Step C), potassium carbonate (3.6 g, 26 mmol) in N,N-dimethylformamide (20 mL) was treated with ethyl bromoacetate (2.1 mL, 18.8 mmol) and the reaction mixture was stirred at ambient temperature for 12 h. The reaction mixture was diluted with ethyl acetate, washed with water, and dried over MgSO4. The reaction mixture was filtered and concentrated under reduced pressure. The crude product was purified by silica gel chromatography using 0-50% ethyl acetate in hexanes as eluant to give 940 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586611B2
Source datasetuspto-grants-2013_11
ORD IDord-0ed21987bd8b4357ab718ce75638c089
Source noteuspto-grants-2013_11