HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928667Generated: October 26, 2026
Phenyl-1-naphthylamine → N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amine
https://huagongshe.com/reaction/1928667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl-1-naphthylamine | HCID 7013 | — |
| Reactant | 4,4'-Dibromobiphenyl | HCID 7110 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amine | HCID 16755312 | 70% |
Reaction Steps
A mixture of 4,4′-dibromobiphenyl (8.46 g=27.4 mmol), Pd(OAc)2 (105 mg=0.18 mmol), dppf (253 mg=0.46 mmol), N-(1-naphthyl)aniline (2.0 g=9.13 mmol) and sodium t-butoxide (1.32 g=13.7 mmol) in dry toluene was placed in a three-necked flask under a nitrogen atmosphere and stirred at 90° C. for 15 h. After cooling, the reaction was quenched by adding water and then extracted by ethyl acetate. The organic layer was dried over anhydrous MgSO4 and evaporated under vacuum. The products were purified by a silica gel column eluted with hexane. White solid of compound 2N was obtained in 70% yield (2.86 g=6.37 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183393B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-445ad050c76a4e5ca7eae9f41f26deb5 |
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| Source note | uspto-grants-2012_05 |
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