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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402759Generated: October 25, 2026

Phenylhydrazine hydrochloride → ethyl 1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/402759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazine hydrochlorideHCID 60962—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantEthyl 2,4,5-trifluorobenzoylacetateHCID 2758933—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Productethyl 1-phenyl-5-(2,4,5-trifluorophenyl)-1H-pyrazole-4-carboxylateHCID 86685264—

Reaction Steps

A solution of ethyl 3-oxo-3-(2,4,5-trifluorophenyl)propanoate (0.326 g, 1.32 mmol) and N,N-dimethyformamide dimethyl acetal in ethanol (5 mL) was heated in a 90° C. oil bath for 3 hours. Upon removal of the volatiles, the residue was dissolved in EtOH (3 mL) and phenylhydrazine hydrochloride salt (191 mg, 1.324 mmol) was added. The mixture was then heated at reflux for 6 hours. The reaction was cooled and diluted with EtOAc and the organic layer was washed with NaHCO3 and brine. The organic phase was dried with Na2SO4, filtered and concentrated to afford the title compound as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742110B2
Source datasetuspto-grants-2014_06
ORD IDord-2c3f4e2ed52c445c8ea94ce06b9794be
Source noteuspto-grants-2014_06