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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021177Generated: October 26, 2026

4-Iodoanisole → N-([1,1'-biphenyl]-4-yl)-N-(4-methoxyphenyl)-[1,1':3',1''-terphenyl]-4'-amine

https://huagongshe.com/reaction/1021177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodoanisoleHCID 69676—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantSodium t-butoxideHCID 23676156—
ReactantN-([1,1'-biphenyl]-4-yl)-[1,1':3',1''-terphenyl]-4'-amineHCID 86762383—
CatalystHexaneHCID 8058—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductN-([1,1'-biphenyl]-4-yl)-N-(4-methoxyphenyl)-[1,1':3',1''-terphenyl]-4'-amineHCID 8676239094%

Reaction Steps

Toluene (200 mL) was bubbled with nitrogen for 15 min, followed by addition of 10% t-Bu3P in hexane (2.9 mL, 1.0 mmol) and Pd2(dba)3 (1.1 g, 1.2 mmol). The mixture was bubbled with nitrogen for 15 min, then N-([1,1′-biphenyl]-4-yl)-[1,1′:3′,1″-terphenyl]-4′-amine (10.6 g, 26.5 mmol), 4-iodoanisole (11.2 g, 48.0 mmol), sodium tert-butoxide (3.5 g, 36.0 mmol) were added. The mixture was bubbled with nitrogen for 15 min and stirred for 16 h at room temperature. 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 30-40% toluene/hexane (containing 0.5% triethylamine) to afford N-([1,1′-biphenyl]-4-yl)-N-(4-methoxyphenyl)-[1,1′:3′,1″-terphenyl]-4′-amine (12.5 g, 94% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716484B1
Source datasetuspto-grants-2014_05
ORD IDord-2f8558c126e34378bcd9258097a7ffb4
Source noteuspto-grants-2014_05