HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163282Generated: November 1, 2026
Water → 2',6'-Dimethylbiphenyl-3-carbaldehyde
https://huagongshe.com/reaction/1163282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | 2,6-Dimethylphenylboronic acid | HCID 583322 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 2',6'-Dimethylbiphenyl-3-carbaldehyde | HCID 23082866 | 97% |
Reaction Steps
3-Bromobenzaldehyde (18.5 g, 100 mmol) and (2,6-dimethylphenyl)boronic acid (21.0 g, 140 mmol) were dissolved in a mixed solvent of 1 M aqueous sodium carbonate solution (200 mL), ethanol (100 mL) and toluene (200 mL). After argon substitution, tetrakis(triphenylphosphine)palladium(0) (5.78 g, 5.00 mmol) was added. The reaction mixture was stirred under an argon atmosphere at 80° C. for 20 hr. The reaction mixture was cooled, and water was added to the reaction mixture. The mixture was diluted with ethyl acetate, and the insoluble material was filtered through celite. The organic layer of the filtrate was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-10% ethyl acetate/hexane) to give the title compound (20.4 g, yield 97%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820837B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-07736b8a08144f1eb2b21fdbdd355f34 |
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| Source note | uspto-grants-2010_10 |
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