HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026557Generated: November 2, 2026
Sodium Carbonate → Benzyl 3-fluoro-2'-hydroxybiphenyl-4-carboxylate
https://huagongshe.com/reaction/1026557
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (2-Hydroxyphenyl)boronic acid | HCID 2773454 | — |
| Reactant | Benzyl 4-bromo-2-fluorobenzoate | HCID 22351348 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Benzyl 3-fluoro-2'-hydroxybiphenyl-4-carboxylate | HCID 68005717 | 89.5% |
Reaction Steps
To a mixed solvent solution of benzyl 4-bromo-2-fluorobenzoate (67.0 g) and 2-hydroxyphenylboronic acid (31.3 g) in 1,2-dimethoxyethane (750 ml) and water (250 ml) were added sodium carbonate (68.7 g) and tetrakis(triphenylphosphine)palladium (12.5 g), followed by stirring under heating at reflux for 5 hours. The reaction solution was brought back to room temperature, and then poured into ice water, followed by extraction with ethyl acetate. The organic layer was washed sequentially with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography, and further washed with hexane to afford benzyl 3-fluoro-2′-hydroxybiphenyl-4-carboxylate (62.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729095B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-59723858dcb4484aa86762041e211582 |
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| Source note | uspto-grants-2014_05 |
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