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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066995Generated: November 3, 2026

tert-Butyl 4-cyano-4-(2,4-difluorophenyl)piperidine-1-carboxylate → 4-(2,4-Difluorophenyl)-piperidine-4-carbonitrile

https://huagongshe.com/reaction/1066995

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-cyano-4-(2,4-difluorophenyl)piperidine-1-carboxylateHCID 18353388—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product4-(2,4-Difluorophenyl)-piperidine-4-carbonitrileHCID 1051320890%

Reaction Steps

To 4-Cyano-4-(2,4-difluorophenyl)-piperidine-1-carboxylic acid tert-butyl ester (0.720 g, 2.42 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 0.484 g (90%) of 4-(2,4-difluorophenyl)-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-9556294d98604d2dbe3c922a4a0f0935
Source noteuspto-grants-2001_06