HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230962Generated: October 30, 2026
3-Nitrophenylboronic Acid → 2-(3-Nitrophenyl)naphthalene
https://huagongshe.com/reaction/2230962
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Nitrophenylboronic Acid | HCID 1677 | — |
| Reactant | 2-Bromonaphthalene | HCID 11372 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 2-(3-Nitrophenyl)naphthalene | HCID 11322633 | 89.7% |
Reaction Steps
To a solution of 2-bromonaphthalene (5.0 g) and tetrakis(triphenylphosphine)palladium(0) (0.56 g) in toluene (50 ml) was added a solution of dihydroxy(3-nitrophenyl)borane (4.44 g) in methanol and 2M sodium carbonate solution in water (12 ml). The resulting mixture was stirred at 80° C. for 4 hours and extracted with ethyl acetate. After evaporation of the solvent, the crude residue was crystallized from hexane to give 3-(2-naphthyl)-1-nitrobenzene (5.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06426345B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-b8f0acea75694a8e8d1fcd770b27c495 |
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| Source note | uspto-grants-2002_07 |
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