HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645489Generated: October 30, 2026
Bromobenzene → 1,4-Diphenylpiperidine-4-carbonitrile
https://huagongshe.com/reaction/645489
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 4-Phenylpiperidine-4-carbonitrile hydrochloride | HCID 3084973 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,4-Diphenylpiperidine-4-carbonitrile | HCID 13046860 | — |
Reaction Steps
To a suspension of 4-phenylpiperidine-4-carbonitrile hydrochloride (6.7 mmol) in toluene (30 mL) are successively added bromobenzene (8.0 mmol), sodium tert-butoxide (17 mmol), tri-o-tolylphosphine (1.3 mmol), and tris(dibenzylideneacetone)dipalladium (0.7 mmol), then the mixture is refluxed for 20 h. The reaction mixture is cooled, diluted with water, then extracted with AcOEt. The organic extracts are washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue is purified by silica gel column chromatography to give the title compound; 1H NMR (CDCl3) δ: 2.12-2.20 (2H, m), 2.23-2.28 (2H, m), 2.94-3.01 (2H, m), 3.86 (2H, d), 6.83 (1H, t), 7.04 (2H, d), 7.22-7.28 (2H, m), 7.36-7.41 (1H, m), 7.45-7.49 (2H, m), 7.56-7.59 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07704996B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-45b9102dabb749708028189b5dcedefc |
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| Source note | uspto-grants-2010_04 |
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