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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477598Generated: October 29, 2026

Sodium Iodide → Ethyl 2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)acetate

https://huagongshe.com/reaction/1477598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-(Trifluoromethyl)pyrazoleHCID 1807034—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductEthyl 2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)acetateHCID 2064143—

Reaction Steps

To a chloroform solution (2 mL) of 3-(trifluoromethyl)-1H-pyrazole (68 mg, 0.50 mmol), potassium carbonate (104 mg, 0.75 mmol) and ethyl bromoacetate (100 mg, 0.60 mmol) were added and the resultant mixture was stirred at 70° C. for 2 hours. To the reaction solution, adequate amount of sodium iodide was added and the resultant mixture was further stirred for 1 day. To the reaction solution, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (147 mg, 0.77 mmol), 1-hydroxybenzotriazole (catalytic amount) and ethanol (500 μL) were added and the resultant mixture was stirred for 2 hours. After completion of the reaction, water was added to the reaction solution and extraction with chloroform from the resultant mixture was performed. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain a crude product of the title compound. The crude product was used in the next reaction as it was.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-c0ab7cc382e44ff9a758c647329e5b2b
Source noteuspto-grants-2016_08