HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531047Generated: October 30, 2026
Potassium Phosphate, Tribasic → 4'-Fluoro-3-methoxy-[1,1'-biphenyl]-4-carbaldehyde
https://huagongshe.com/reaction/531047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | 4-Bromo-2-methoxybenzaldehyde | HCID 11053041 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4'-Fluoro-3-methoxy-[1,1'-biphenyl]-4-carbaldehyde | HCID 22566727 | 59.8% |
Reaction Steps
Palladium acetate (2.61 g) was added to a mixture of 4-bromo-2-methoxybenzaldehyde (25.0 g), tripotassium phosphate (74.0 g), (4-fluorophenyl)boronic acid (24.4 g), tricyclohexylphosphine (20% toluene solution, 41.3 mL), toluene (250 mL), and water (125 mL), and the resultant mixture was stirred at 90° C. for 3 hours in an argon atmosphere. The reaction mixture was allowed to cool to room temperature, and then, the organic layer was separated. The aqueous layer was subjected to extraction with ethyl acetate. Combined organic layers were washed with water and saturated saline in this order and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was crystallized from methanol (150 mL) to obtain the title compound (16.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353108B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-9a78c1f836294f7d85f24f5a351b8ce9 |
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| Source note | uspto-grants-2016_05 |
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