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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396775Generated: 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/396775

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 numberUS06608095B2
Source datasetuspto-grants-2003_08
ORD IDord-52d886c3c79848138fc2c244c12c65ba
Source noteuspto-grants-2003_08