HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404381Generated: October 27, 2026
Potassium Phosphate, Tribasic → 2'-Fluoro-2-formyl-5'-methoxy-biphenyl-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/404381
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Fluoro-5-methoxyphenylboronic acid | HCID 4157211 | — |
| Reactant | Methyl 3-formyl-4-(trifluoromethylsulfonyloxy)benzoate | HCID 57467631 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 2'-Fluoro-2-formyl-5'-methoxy-biphenyl-4-carboxylic acid methyl ester | HCID 57467630 | 100.6% |
Reaction Steps
To a round bottle flask, was added methyl 3-formyl-4-(trifluoromethylsulfonyloxy)benzoate (6300 mg, 20 mmol), 2-fluoro-5-methoxyphenylboronic acid (10 g, 61 mmol), potassium phosphate tribasic (6.6 mL, 81 mmol) (granular) and tetrakis(triphenylphosphine)palladium (2.3 g, 2.0 mmol). The flask was flushed with nitrogen and then 40 mL of DME was added. The resulting mixture was then heated at 90° C. for 6 hours. The reaction mixture was diluted with EtOAc and water. The organic phase was washed with water and brine and then dried over anhydrous sodium sulfate. After filtration, the organic solvent was removed in vacuo to give a residue which was purified by CombiFlash® chromatography to give a yellow solid (5.80 g, 100%). MS ESI m/e: 289.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748462B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-ea679f24b21e4940a472ef79b73047b5 |
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| Source note | uspto-grants-2014_06 |
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