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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868790Generated: October 31, 2026

4-Aminobiphenyl → HCID 58672293, compound

https://huagongshe.com/reaction/868790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobiphenylHCID 7102—
Reactant1~4~-Bromo-1~1~,2~1~:2~3~,3~1~-terphenylHCID 14452534—
ReactantSodium t-butoxideHCID 23676156—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventTolueneHCID 1140—
ProductHCID 58672293HCID 5867229374.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08968883B2
Source datasetuspto-grants-2015_03
ORD IDord-9e56fd8d9f8c464c8a8900f608571574
Source noteuspto-grants-2015_03