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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842890Generated: November 2, 2026

4,4,4-Trifluoro-3-oxobutanenitrile → HCID 70816398, compound

https://huagongshe.com/reaction/1842890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,4-Trifluoro-3-oxobutanenitrileHCID 13843540—
ReactantHCID 86672143HCID 86672143—
SolventEthanolHCID 702—
ProductHCID 70816398HCID 7081639824.1%

Reaction Steps

To a stirred solution of 4,4,4-trifluoro-3-oxobutanenitrile (1.64 g, 11.96 mmol, 1.0 eq) in ethanol (15 mL) was added (3-chloro-2-methoxyphenyl)hydrazine (2.5 g, 11.96 mmol, 1.0 eq) and the mixture was refluxed for 3 h. Ethanol was evaporated, the mixture diluted with water and extracted with ethyl acetate (300 mL×2), dried (Na2SO4), evaporated again under vacuum. The crude product was purified by CC using EtOAc/PE (1:4) as eluent to get 1-(3-chloro-2-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-5-amine (0.84 g, 24%, yellow oil; TLC system: EtOAc/PE (2:3), Rf: 0.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946204B2
Source datasetuspto-grants-2015_02
ORD IDord-ca68d1725d5c4a96a18a31cfb6dc4343
Source noteuspto-grants-2015_02