HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741053Generated: October 31, 2026
Triethylamine → 3-Methyl 6-methyl[1,1′-biphenyl]-3,4′-dicarboxylate
https://huagongshe.com/reaction/1741053
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Carboxyphenylboronic Acid | HCID 312183 | — |
| Reactant | Methyl 3-bromo-4-methylbenzoate | HCID 7015747 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methyl 6-methyl[1,1′-biphenyl]-3,4′-dicarboxylate | HCID 21833756 | 85% |
Reaction Steps
A stirred solution of methyl 3-bromo-4-methylbenzoate (2.6 g, 0.011 mole) in dry DMF (20 ml) under argon was treated with 4-boronobenzoic acid (1.85 g, 0.011 mole) and tetrakis (triphenylphosphine) palladium(0) (400 mg), followed by triethylamine (4.68 ml, 0.046 mole). The mixture was heated at 100° C. for 18 hours, then concentrated in vacuo. The residue was treated with ethyl acetate and extracted with 10% NaHCO3 solution. The basic extract was acidified with dil. HCl and extracted with ethyl acetate. The extract was dried (Na2SO4) and concentrated in vacuo to afford the title compound as a light orange solid (2.12 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05972951 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-4c381ef49be94e3ab0565b01df8e6d7d |
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| Source note | uspto-grants-1999_10 |
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