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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21390Generated: October 25, 2026

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

https://huagongshe.com/reaction/21390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Bromoethyl)-1,2-dichlorobenzeneHCID 15149389—
Reactant3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidineHCID 22853758—
SolventAcetonitrileHCID 6342—
Product3-(R)-(1-cyano-1,1-diphenylmethyl)-1--(3,4-dichlorophenethyl)piperidineHCID 21311312—

Reaction Steps

A mixture containing 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)piperidine (0.28 g), 3,4-dichlorophenethyl bromide (0.255 g), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 8 hours. The mixture was partitioned between dichlorometbane (30 ml) and 10% aqueous potassium carbonate (20 ml), the layers separated and the aqueous layer extracted with dichloromethane (3×70 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated inn vacuo to give an oil which was purified by column chromatograpby on silica eluting with dichloromethane containing hexane (30%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound, yield 0.233 g, m.p. 139°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422358
Source datasetuspto-grants-1995_06
ORD IDord-2b313ee99fad42879db9e4efd08876bc
Source noteuspto-grants-1995_06