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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14352Generated: October 26, 2026

Tris(4-bromophenyl)amine → 4-(Thiophen-2-yl)-N,N-bis(4-(thiophen-2-yl)phenyl)aniline

https://huagongshe.com/reaction/14352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(4-bromophenyl)amineHCID 258027—
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-(Thiophen-2-yl)-N,N-bis(4-(thiophen-2-yl)phenyl)anilineHCID 1531542885%

Reaction Steps

First, 1 g (2 mmol) of tris(4-bromophenyl)amine (Aldrich) was dissolved in 100 ml of toluene, and then 2.9 ml (4.5 eq.) of 2-tributylstannylthiophene and 27 mg (1.1%) of Pd(PPh3)4 were added thereto. The mixture was refluxed under a nitrogen atmosphere for 12 hours. The reaction mixture was allowed to cool to room temperature, washed with brine twice, and dried over MgSO4. After the solvent was evaporated, the obtained residue was washed with petroleum ether (PE), and dried, affording 0.87 g (yield: 85%) of tris[4-(2-thienyl)phenyl]amine as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07731796B2
Source datasetuspto-grants-2010_06
ORD IDord-7c16fafe58124208947e5b9c94c8c2d7
Source noteuspto-grants-2010_06