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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21389Generated: October 25, 2026

Potassium Carbonate → 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-(4-methylphenethyl)piperidine

https://huagongshe.com/reaction/21389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methylphenethyl bromideHCID 570680—
Reactant3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidineHCID 22853758—
SolventAcetonitrileHCID 6342—
Product3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-(4-methylphenethyl)piperidineHCID 22853755—

Reaction Steps

A mixture containing 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)piperidine (1 g), 4-methylphenethyl bromide (0.72 g) , anhydrous potassium carbonate (1.5 g) and acetonitrile (25 ml) was heated under reflux for 5 hours. The mixture was partitioned between dichloromethane (50 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (3×30 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with hexane containing dichloromethane (30% up to 70%) then dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound as colourless rbombs, yield 1 g, m.p. 110°-113° C. [α]D25 +14.7 (c 1.0 CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422358
Source datasetuspto-grants-1995_06
ORD IDord-8ab51ca1da144046aa59111bb83dc966
Source noteuspto-grants-1995_06