HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422256Generated: October 31, 2026
1-Bromo-2-methylnaphthalene → 3-(2-Methylnaphthalen-1-yl)benzaldehyde
https://huagongshe.com/reaction/2422256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-methylnaphthalene | HCID 75754 | — |
| Reactant | 3-Formylphenylboronic acid | HCID 2734356 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 3-(2-Methylnaphthalen-1-yl)benzaldehyde | HCID 23083031 | 65% |
Reaction Steps
1-Bromo-2-methylnaphthalene (3.32 g, 15.0 mmol) and (3-formylphenyl)boronic acid (2.13 g, 15.0 mmol) was dissolved in a mixture of 1 M sodium carbonate aqueous solution (30 mL), ethanol (15 mL) and toluene (30 mL) and, after argon substitution, tetrakis(triphenylphosphine)palladium (0) (0.867 g, 0.750 mmol) was added. The reaction mixture was stirred under an argon atmosphere at 80° C. for 24 hrs. The reaction mixture was cooled, diluted with water and 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-20% ethyl acetate/hexane) to give the title compound (2.39 g, yield 65%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960369B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-052080beb3114ebfaa9997b2d51d07d0 |
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| Source note | uspto-grants-2011_06 |
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