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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167723Generated: November 2, 2026

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

https://huagongshe.com/reaction/1167723

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 dichloromethane (5 mL), trifluoroacetic acid (2 mL) 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 numberUS06620815B1
Source datasetuspto-grants-2003_09
ORD IDord-7c194100479b4d54a77bb5ab8508ae7d
Source noteuspto-grants-2003_09