HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974962Generated: October 30, 2026
Phenethyl bromide → 4-(2-Carbamoyl-2,2-diphenylethyl)-1-phenethylpiperidine
https://huagongshe.com/reaction/974962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Carbamoyl-2,2-diphenylethyl)piperidine | HCID 19970199 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(2-Carbamoyl-2,2-diphenylethyl)-1-phenethylpiperidine | HCID 9844577 | 49% |
Reaction Steps
A mixture of 4-(2-carbamoyl-2,2-diphenylethyl)piperidine (300 mg, 0.97 mmol) (Preparation 3), phenethyl bromide (198 mg, 1.07 mmol) and potassium carbonate (400 mg) in acetonitrile (10 ml) was heated under reflux for 6 hours, allowed to cool to room temperature and evaporated. The residue was partitioned between dichloromethane and 10% aqueous potassium carbonate solution and the aqueous layer was extracted twice into dichloromethane. The combined organic layers were dried over magnesium sulphate and evaporated. The residue was purified by chromatography on silica using dichloromethane plus 0-10% methanol as eluant. Appropriate fractions were combined and evaporated to give the title compound (195 mg, 49%) as a colourless foam, which was characterised as a hydrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607950 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-c10e94ed41c246c99adeef3f417d9968 |
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| Source note | uspto-grants-1997_03 |
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