HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893152Generated: October 31, 2026
Water → Methyl 6-methoxy-[1,1'-biphenyl]-3-carboxylate
https://huagongshe.com/reaction/1893152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Methyl 3-bromo-4-methoxybenzoate | HCID 611662 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 6-methoxy-[1,1'-biphenyl]-3-carboxylate | HCID 11010121 | 95% |
Reaction Steps
To a solution of methyl 3-bromo-4-methoxybenzoate (13 g, 53 mmol) in toluene (500 mL), methanol (65 mL), and water (106 mL) was added phenyl boronic acid (7.8 g, 63.6 mmol) and potassium carbonate (14.6 g, 106 mmol) and bubbled with argon for 6 min. Tetrakis(triphenylphosphine)palladium(0) (370 mg) was added and bubbled with argon for another 2 min. The reaction mixture was then heated to 95° C. for 20 h with stirring. After cooling to RT, the two phases were separated and the aqueous layer was extracted with ether, dried with magnesium sulfate, and concentrated. Purification by MPLC (5% ethyl acetate in hexanes) gave 12.2 g of the desired product as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513220B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a0abcecc903e432689d0d74e96949149 |
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| Source note | uspto-grants-2013_08 |
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