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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280775Generated: October 27, 2026

Water → 4-{1-[Bis(2-chlorophenyl)-methyl)-piperidin-4-yl}-butyronitrile

https://huagongshe.com/reaction/1280775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantBis(2-chlorophenyl)-bromomethaneHCID 826777—
Reactant4-(Piperidin-4-yl)butanenitrile hydrochlorideHCID 18425704—
SolventAcetoneHCID 180—
Product4-{1-[Bis(2-chlorophenyl)-methyl)-piperidin-4-yl}-butyronitrileHCID 18425745—

Reaction Steps

20 g (106 mmol) 4-(3-cyanoprop-1-yl)-piperidin hydrochloride, 40.2 g (127 mmol) bis(2-chlorophenyl)-bromomethane and 35.2 g (254 mmol) potassium carbonate are heated to boiling in 90 ml acetone for six hours. After cooling, the mixture is freed from solution under vacuum. The residue is dispersed between 90 ml tolueneand 90 ml water. The aqueous phase is extracted with 10 ml tolueneand the combined organic phases are washed with 10 ml water. The organic phase is concentrated and the residue is chromatographically purified over silica gel with CHCL3. Yield: 11.2 g (27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451816B1
Source datasetuspto-grants-2002_09
ORD IDord-8bbe8f62ff014d25aab7bb8178ea63db
Source noteuspto-grants-2002_09