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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181571Generated: November 2, 2026

Hydrochloric Acid → HCID 22480374, compound

https://huagongshe.com/reaction/1181571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedioneHCID 67594—
ReactantBenzylhydrazine dihydrochlorideHCID 146540—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductHCID 22480374HCID 22480374105.1%

Reaction Steps

To a solution of 50 g (0.240 mol) 4,4,4-trifluoro-1-(2-furyl)-1,3-butanedione in 24 ml (0.024 mol) 1M solution of hydrogen chloride in ethanol and further 520 ml EtOH was added. 50 g (0.248 mol) benzylhydrazine dihydrochloride in small portion at room temperature. The reaction mixture was then heated under reflux for 7 h. After cooling to room temperature the reaction mixture was neutralized with saturated NaHCO3, the EtOH was distilled off and the residual oil/water mixture was extracted with 300 ml dichloromethane. The organic phase was washed twice with 100 ml water and dried over Na2SO4 and concentrated in vacuo to give 73.7 g 1-benzyl-5-furan-2-yl-3-trifluoromethyl-1H-pyrazole as a brown oil which was used crude for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285569B2
Source datasetuspto-grants-2007_10
ORD IDord-e02d8de21729451080a51b6c23d17456
Source noteuspto-grants-2007_10