Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066998Generated: November 3, 2026

tert-Butyl 4-cyano-4-(2,4-dichlorophenyl)piperidine-1-carboxylate → 4-(2,4-Dichlorophenyl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/1066998

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-cyano-4-(2,4-dichlorophenyl)piperidine-1-carboxylateHCID 49760258—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product4-(2,4-Dichlorophenyl)piperidine-4-carbonitrileHCID 2299355999.6%

Reaction Steps

To 4-cyano-4-(2,4-dichlorophenyl)piperidine-1-carboxylic acid tert-butyl ester (0.620 g, 1.74 mmol) in 5 ml of dichloromethane, 2 ml of trifluoroacetic acid was added and the solution stirred at room temperature for 1 hour. The solution was concentrated, neutralized with 10% KOH solution and extracted into 25 ml of dichloromethane. The organic layer was dried over sodium sulfate, filtered and concentrated to give 0.442 g (99%) of 4-(2,4-dichlorophenyl)piperidine-4-carbonitrile which was used as such for the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245773B1
Source datasetuspto-grants-2001_06
ORD IDord-70e4be20d47f414e8dd6636afcd8db1d
Source noteuspto-grants-2001_06