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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497215Generated: October 26, 2026

1-(4-Bromophenyl)-4,4,4-trifluorobutane-1,3-dione → 5-(4-bromophenyl)-1-[3-fluoro-4-(methylsulfonyl)phenyl]-3-(trifluoromethyl)-1H-pyrazole

https://huagongshe.com/reaction/497215

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 2771477—
Reactant[3-Fluoro-4-(methylsulfonyl)phenyl]hydrazine hydrochlorideHCID 22316658—
SolventEthanolHCID 702—
Product5-(4-bromophenyl)-1-[3-fluoro-4-(methylsulfonyl)phenyl]-3-(trifluoromethyl)-1H-pyrazoleHCID 2231671886.6%

Reaction Steps

[3-fluoro-4-(methylsulfonyl)phenyl]hydrazine hydrochloride (0.354 g, 1.47 mmol) was added to a solution of 4,4,4-Trifluoro-1-(4-bromophenyl)butane-1,3-dione (0.395 g. 1.34 mmol) in EtOH (20 mL). The mixture was heated at reflux temperature for 17 hours and cooled down to room temperature. The reaction mixture was concentrated in vacuo, and the residue was taken up in ethyl acetate, washed with water and brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by flash chromatography eluting with hexane/ethyl acetate (3/1). The resulting solid was recrystallized from ethyl acetate/hexane to give the subtitle compound (0.537 g, 86.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949536B2
Source datasetuspto-grants-2005_09
ORD IDord-81ba5977e8a44ff98d038b27a65b7390
Source noteuspto-grants-2005_09