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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzophenone | HCID 7030 | — |
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (4-(Diphenylamino)phenyl)(phenyl)methanone | HCID 10545746 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476474B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-29c0f90b8e4241edb834ac69b649a70b |
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| Source note | uspto-grants-2013_07 |
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