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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446213Generated: October 27, 2026

4-Bromobenzophenone → (4-(Diphenylamino)phenyl)(phenyl)methanone

https://huagongshe.com/reaction/446213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzophenoneHCID 7030—
ReactantDiphenylamineHCID 11487—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
SolventTolueneHCID 1140—
Product(4-(Diphenylamino)phenyl)(phenyl)methanoneHCID 1054574684%

Reaction Steps

(4-bromophenyl)(phenyl)methanone (5.0 g, 19.2 mmol) and diphenylamine (4.2 g, 25.0 mmol) were dissolved in 150 mL of toluene under a nitrogen atmosphere, and then tris(benzylidene acetone dipalladium) (0.4 g, 0.4 mmol) was added thereto under nitrogen. Also, P(t-Bu)3 (0.8 g, 3.8 mmol) was added to the reaction mixture solution, followed by addition of NaOBut (5.5 g, 57.7 mmol). The reaction mixture solution was refluxed and stirred for 24 hours. After the reaction was over, the reaction mixture solution was filtered through a thin silica pad at a high temperature to thereby remove palladium. The filtrate was concentrated, and passed through a silica gel column by using hexane-dichloromethane 7:3 as an eluant. After the solvent was removed, the residue material was dried in vacuum to thereby obtain a white solid (5.6 g, yield: 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476474B2
Source datasetuspto-grants-2013_07
ORD IDord-29c0f90b8e4241edb834ac69b649a70b
Source noteuspto-grants-2013_07