HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572543Generated: November 1, 2026
Water → Methyl 2-(methoxymethyl)-2'-methyl-[1,1'-biphenyl]-4-carboxylate
https://huagongshe.com/reaction/572543
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylphenyl boronic acid | HCID 2733267 | — |
| Reactant | Methyl 4-bromo-3-(methoxymethyl)benzoate | HCID 58554220 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(methoxymethyl)-2'-methyl-[1,1'-biphenyl]-4-carboxylate | HCID 58554139 | — |
Reaction Steps
Methyl 4-bromo-3-(methoxymethyl)benzoate, (40 g; 154 mmol), o-tolylboronic acid (23 g; 170 mmol), K2CO3 (107 g; 772 mmol), tetrakis(triphenylphosphine)palladium (0) (1.8 g; 1.5 mmol) were taken up in toluene (200 mL) and water (200 mL) under N2 atmosphere. The reaction mixture was purged with vacuum, then degassed with N2 and then refluxed for 1 hour. The reaction mixture was cooled to RT, filtered over a pad of celite and washed with EtOAc (1 L). The filtrate was concentrated, affording a yellow oil which was taken in EtOAc (800 mL). The organic layer was washed with a saturated aqueous solution of NaHCO3 solution (250 mL), water (250 mL) and brine (250 mL), dried over MgSO4 and concentrated affording the title compound as a yellow oil used without further purification (42 g, quantitative). HPLC (Method A) Rt 5.34 min (Purity: 89.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029405B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-f8a7ac5b189f435a9fefb4ee7e25efd0 |
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| Source note | uspto-grants-2015_05 |
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