Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043754Generated: October 31, 2026

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

https://huagongshe.com/reaction/2043754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant5-ethyl-3-(trifluoromethyl)-1H-pyrazoleHCID 23006209—
SolventDimethylformamideHCID 6228—
Productethyl 5-ethyl-3-(trifluoromethyl)-1H-pyrazole-1-acetateHCID 6746424463%

Reaction Steps

To a solution of 5-ethyl-3-(trifluoromethyl)-1H-pyrazole (1.39 g, 8.5 mmol) (i.e. the product of Example 16, Step A) in N,N-dimethylformamide (10 mL) was added potassium carbonate (2.3 g) and ethyl bromoacetate (1.4 mL, 12.6 mmol). The reaction mixture was stirred at room temperature overnight. The resulting solids were filtered off and the filtrate was diluted with ethyl acetate, washed with water and dried over MgSO4. The resulting solution was concentrated under reduced pressure to give 1.34 g of the title compound. This compound was of sufficient purity to use in subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586611B2
Source datasetuspto-grants-2013_11
ORD IDord-9080a836df1240f8a3ceff46ce2c9b6b
Source noteuspto-grants-2013_11