Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843020Generated: November 3, 2026

Hydrazine, dihydrochloride → 3-(Trifluoromethyl)pyrazole

https://huagongshe.com/reaction/1843020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, dihydrochlorideHCID 17548—
Reactant(3E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-oneHCID 5709222—
ReactantEthyl acetate hexaneHCID 21226206—
SolventEthanolHCID 702—
Product3-(Trifluoromethyl)pyrazoleHCID 1807034—

Reaction Steps

Hydrazine dihydrochloride (225 g, 2.14 mol) in ethanol (1400 mL) was stirred well. TEA (185.4 mL, 1.34 mol) was added drop wise for 45 min at ambient temperature. Then (E)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one (225 g, crude) was added drop wise at room temperature and the overall reaction mixture was refluxed overnight. Progress of the reaction was monitored by TLC (20% ethyl acetate/hexane, Rf˜0.4). On completion of the reaction, ethanol was distilled off completely, residue was taken in ice water (500 mL) and the product extracted with ethyl acetate (2×400 mL). Combined extract was washed with ice water (300 mL), dried over sodium sulfate and concentrated under reduced pressure to yield 3-(trifluoromethyl)-1H-pyrazole as a off white solid (175 g, crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946204B2
Source datasetuspto-grants-2015_02
ORD IDord-39c58c780c7c49e0bbd205b45820b6aa
Source noteuspto-grants-2015_02