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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021175Generated: November 1, 2026

1,4-Dibromobenzene → HCID 86762388, compound

https://huagongshe.com/reaction/1021175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantSodium t-butoxideHCID 23676156—
ReactantBiphenyl-4-yl- biphenyl-2-yl-amin;N-{[1,1'-biphenyl]-4-yl}-[1,1'-biphenyl]-2-amineHCID 86762387—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 86762388HCID 8676238887%

Reaction Steps

Toluene (500 mL) was bubbled with nitrogen for 15 min, followed by addition of triphenylphosphine (0.4 g, 1.7 mmol) and Pd(OAc)2 (0.10 g, 0.42 mmol). The mixture was bubbled with nitrogen for 15 min, then N-([1,1′-biphenyl]-4-yl)-[1,1′-biphenyl]-2-amine (6.7 g, 21.0 mmol), 1,4-dibromobenzene (14.9 g, 63.0 mmol), sodium tert-butoxide (4.0 g, 42.0 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 (containing 0.5% triethylamine). The solvent was removed in vacuo and the residue was purified by flash chromatography using 10-20% toluene/hexane (containing 0.5% triethylamine) to afford N-([1,1′-biphenyl]-4-yl)-N-(4-bromophenyl)-[1,1′-biphenyl]-2-amine (8.7 g, 87% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716484B1
Source datasetuspto-grants-2014_05
ORD IDord-fd0095f01a244f86af9fc3ad4e05623c
Source noteuspto-grants-2014_05