HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782655Generated: October 25, 2026
Ethanol → [1,1'-Biphenyl]-4-carboxylicacid, 4'-bromo-, methyl ester
https://huagongshe.com/reaction/1782655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 4-iodobenzoate | HCID 69273 | — |
| Reactant | (4-Bromophenyl)boronic acid | HCID 79599 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [1,1'-Biphenyl]-4-carboxylicacid, 4'-bromo-, methyl ester | HCID 737627 | — |
Reaction Steps
A mixture of methyl 4-iodobenzoate, 9.38 g (35.8 mmol), 4-bromophenylboronic acid 7.18 g (35.8 mmol), Pd(PPh3)4, 2.07 g (1.79 mmol), in 180 mL of toluene and 100 mL of ethanol was heated to obtain a clear solution. To the solution was added 30 mL of 4.0M aq. Na2CO3. The reaction mixture refluxed for 4 h at 80° C. The mixture was cooled to room temperature and diluted with 300 mL ethyl acetate. The organic layer was washed with 2×300 mL portions of water, 2×300 mL portions of sat. aq. NaCl, and dried (MgSO4). After the solution was concentrated, the residue was purified by column chromatography (eluted with 7% EtOAc-Heptane) to afford the desired product in 7.8 g (78%) as a white solid. 1H NMR (CDCl3) 8.10 (d, 2H, J=9.0 Hz), 7.62 (d, 2H, J=9.0 Hz), 7.59 (d, 2H, J=9.3 Hz), 7.48 (d, 2H, J=9.3 Hz), 3.95 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07498356B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-f8b428ec23fd4237a150471823319346 |
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| Source note | uspto-grants-2009_03 |
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