HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404364Generated: October 27, 2026
Potassium Phosphate, Tribasic → 2'-Fluoro-2-formyl-5'-methoxy-biphenyl-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/404364
Participants
| Role | Name | HCID | Charge |
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| 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) (commercially available from Sigma-Aldrich, St. Louis, Mo., USA), 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, DME was added, and the mixture was 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 chromatography to give the product as 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-85797cf46328462090f0904f7df003b1 |
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| Source note | uspto-grants-2014_06 |
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