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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Furan-2-boronic acid | HCID 2734357 | — |
| Reactant | 1-(4-Bromophenyl)-4,4,4-trifluorobutane-1,3-dione | HCID 2771477 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4,4,4-Trifluoro-1-[4-(2-furyl)phenyl]butane-1,3-dione | HCID 12114160 | 61.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608095B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-be658cb2eabf477eae42fa8bc565ba85 |
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| Source note | uspto-grants-2003_08 |
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