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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238680Generated: October 29, 2026

Potassium Carbonate → ethyl 5-bromo-3-(trifluoromethyl)-1H-pyrazole-1-acetate

https://huagongshe.com/reaction/238680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl iodoacetateHCID 12183—
ReactantHCID 178506065HCID 178506065—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productethyl 5-bromo-3-(trifluoromethyl)-1H-pyrazole-1-acetateHCID 68745175—

Reaction Conditions

Temperature95 °C

Reaction Steps

A suspension of 5-bromo-3-(trifluoromethyl)-1H-pyrazole (i.e. the product of Example 11, Step B) (2.73 g, 12.7 mmol) and potassium carbonate (2.0 g, 14.5 mmol) in N,N-dimethylformamide (20 mL) was treated with ethyl iodoacetate (3.0 ml, 25.3 mmol), and the resulting mixture was stirred at 95° C. for 3 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 2.84 g of the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642634B2
Source datasetuspto-grants-2014_02
ORD IDord-5c45e7e55ad94074b5e0d074123548b0
Source noteuspto-grants-2014_02