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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924759Generated: November 1, 2026

4-(4-Chlorophenyl)-4-(4-iodophenyl)piperidine → 4-[4-(4-Chlorophenyl)piperidin-4-yl]benzonitrile

https://huagongshe.com/reaction/924759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenyl)-4-(4-iodophenyl)piperidineHCID 59331974—
ReactantHCID 178418546HCID 178418546—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[4-(4-Chlorophenyl)piperidin-4-yl]benzonitrileHCID 6723576916%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 4-(4-chloro-phenyl)-4-(4-iodo-phenyl)-piperidine and copper (I) cyanide in DMF was heated at 140° C. under nitrogen for 6 hours then allowed to cool. The mixture was diluted with ethyl acetate, washed with a mixture of conc. ammonia and brine (×5), dried (MgSO4), filtered and concentrated to give a residue which was partially purified by column chromatography (SiO2), eluting with a gradient of 2M ammonia in methanol (5% to 10%) and dichloromethane to afford the title compound (46 mg, <16%). This was taken on to the next reaction without further purification. LCMS (PS-A2) Rt 2.39 min [M+H]+ 297.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283226B2
Source datasetuspto-grants-2016_03
ORD IDord-f332ee8dc2454806b2a5dd3fff21bb82
Source noteuspto-grants-2016_03