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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021171Generated: November 1, 2026

4-Bromobiphenyl → HCID 86762384, compound

https://huagongshe.com/reaction/1021171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobiphenylHCID 7101—
Reactant2,6-diphenylanilineHCID 11010226—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 86762384HCID 86762384471.7%

Reaction Steps

Xylene (250 mL) was bubbled with nitrogen for 15 min, followed by addition of 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (4.6 g, 11.2 mmol) and Pd2(dba)3 (2.6 g, 2.8 mmol). The mixture was bubbled with nitrogen for 15 min, then [1,1′:3′,1″-terphenyl]-2′-amine (13.7 g, 56.0 mmol), 4-bromobiphenyl (13.0 g, 56.0 mmol), sodium tert-butoxide (10.8 g, 112.0 mmol) were added. The mixture was bubbled with nitrogen for 15 min and refluxed for 12 h. After cooling, the reaction mixture was filtered through a silica pad and washed with toluene. The solvent was removed in vacuo and the residue was purified by flash chromatography using 30-40% toluene/hexane to afford N-([1,1′-biphenyl]-4-yl)-[1,1′:3′,1″-terphenyl]-2′-amine (21.0 g, 93% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716484B1
Source datasetuspto-grants-2014_05
ORD IDord-359e52bcfd01480f961ed9816339ce3e
Source noteuspto-grants-2014_05