HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868790Generated: October 31, 2026
4-Aminobiphenyl → HCID 58672293, compound
https://huagongshe.com/reaction/868790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobiphenyl | HCID 7102 | — |
| Reactant | 1~4~-Bromo-1~1~,2~1~:2~3~,3~1~-terphenyl | HCID 14452534 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Catalyst | Tris(dibenzylideneacetone) dipalladium | HCID 9832798 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58672293 | HCID 58672293 | 74.3% |
Reaction Steps
In a drybox, 4-aminobiphenyl (0.542 g) and 4-bromo-1,1′:3′,1″-terphenyl (0.89 g) were combined in a round-bottom flask and dissolved in 10 ml of dry toluene. Tris(tert-butyl)phosphine (0.022 g, 0.11 mmol) and tris(dibenzylideneacetone) dipalladium(0) (0.05 g, 0.055 mmol) were dissolved in 10 ml of dry toluene and stirred for 5 minutes. The catalyst solution was added to the reaction mixture, stirred for 2 minutes and was followed by sodium tert-butoxide (0.32 g, 3.3 mmol). Flask was capped and left to stir in the drybox overnight at room temperature. Next day, reaction mixture was taken out of the box and filtered through a one-inch plug of silica gel topped with celite, washing with 500 ml of dichloromethane. Removal of volatiles under reduced pressure gave a yellow solid. Crude product was purified by trituration with diethyl ether to give 0.85 g (73%) of a white solid. Structure was confirmed by 1H NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08968883B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9e56fd8d9f8c464c8a8900f608571574 |
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| Source note | uspto-grants-2015_03 |
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