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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491470Generated: October 27, 2026

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

https://huagongshe.com/reaction/491470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantEthyl 2-(1-benzylpiperidin-4-ylidene)-2-cyanoacetateHCID 424752—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-Benzyl-4-(cyanomethyl)piperidine-4-carbonitrileHCID 1284765481.2%

Reaction Steps

To a solution of (1-benzyl-piperidin-4-ylidene)-cyano-acetic acid ethyl ester (112.9 g, 0.40 mol) in EtOH (500 ml) and H2O (100 ml), potassium cyanide (64.6 g, 0.99 mol) is added at ambient temperature. The reaction mixture is stirred at 65 C.° for 24 h. After removal of EtOH, H2O is added to the residue. The waster phase is extracted with diethyl ether. The combined extracts are washed with H2O and brine, dried over sodium sulfate and evaporated down to give 77.7 g of 1-benzyl-4-cyanomethyl-piperidine-4-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531546B2
Source datasetuspto-grants-2009_05
ORD IDord-d14765825f544761824cd3df324f0815
Source noteuspto-grants-2009_05