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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212998Generated: November 2, 2026

Potassium Cyanide → 1-Benzyl-4-(dimethylamino)piperidine-4-carbonitrile

https://huagongshe.com/reaction/2212998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant1-Benzyl-4-piperidoneHCID 19220—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-Benzyl-4-(dimethylamino)piperidine-4-carbonitrileHCID 1645391596.1%

Reaction Steps

A solution of 1-(phenylmethyl)-4-piperidone (9.46 g, 50 mmol) in ethanol (20 mL) was added slowly to a stirred solution of potassium cyanide (3.58 g, 55 mmol) and dimethylamine hydrochloride (4.89 g, 60 mmol) in water (60 mL). The mixture was stirred at room temperature for 68 hours, then water (100 mL) was added. The solid was collected, suspended in aqueous sodium hydrogen carbonate (saturated, 100 mL) and water (50 mL) and extracted with dichloromethane (3×100 mL). The combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure to give the the title compound as a cream solid (11.69 g, 96%). m/z (ES+) 244 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105507B2
Source datasetuspto-grants-2006_09
ORD IDord-291adae48e0342db817d4c15949f9bac
Source noteuspto-grants-2006_09