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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396765Generated: October 26, 2026

Sodium Bicarbonate → 4,4,4-Trifluoro-1-[4-(2-furyl)phenyl]butane-1,3-dione

https://huagongshe.com/reaction/396765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantFuran-2-boronic acidHCID 2734357—
Reactant1-(4-Bromophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 2771477—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4,4,4-Trifluoro-1-[4-(2-furyl)phenyl]butane-1,3-dioneHCID 1211416061.2%

Reaction Steps

To a stirred solution of 4,4,4-trifluoro-1-(4-bromophenyl)butane-1,3-dione (1 g, 3.39 mmol, prepared according to the method of J. Med. Chem., 1997, 40, 1347) in DME (40 mL) was added furan-2-boronic acid (0.455 g, 4.07 mmol), bis(triphenylphosphine) palladium(II)chloride (0.271 g, 0.386 mmol) and saturated NaHCO3 solution (12 mL) at room temperature under nitrogen. The mixture was heated at reflux temperature for 5 hours, and cooled down to room temperature. The reaction mixture was filtered through celite, the filtrate was poured into water and the whole was extracted with ethyl acetate (30 mL×3). The organic layer was washed with brine, dried over sodium sulfate, and concentrated in vacuo . The residue was purified by flash chromatography eluting with hexane/ethyl acetate (3/1) to give the subtitle compound (0.586 g, 61.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608095B2
Source datasetuspto-grants-2003_08
ORD IDord-be658cb2eabf477eae42fa8bc565ba85
Source noteuspto-grants-2003_08