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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Carbamoyl-2,2-diphenylethyl)piperidineHCID 19970199—
SolventAcetonitrileHCID 6342—
Product4-(2-Carbamoyl-2,2-diphenylethyl)-1-phenethylpiperidineHCID 984457749%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607950
Source datasetuspto-grants-1997_03
ORD IDord-c10e94ed41c246c99adeef3f417d9968
Source noteuspto-grants-1997_03