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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596679Generated: October 31, 2026

Potassium Cyanide → Benzyl 4-benzylamino-4-cyanopiperidine-1-carboxylate hydrochloride

https://huagongshe.com/reaction/1596679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantBenzylammonium chlorideHCID 2724127—
ReactantBenzyl 2-oxopiperidine-1-carboxylateHCID 11096497—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductBenzyl 4-benzylamino-4-cyanopiperidine-1-carboxylate hydrochlorideHCID 23435758—

Reaction Steps

11.65 g (50 mmol) N-(benzyloxycarbonyl)piperidone (prepared from 4-piperidone and benzyl chloroformate according to Chem. Pharm. Bull. 1982, 30, 1084) and 7.2 g (50 mmol) benzylamine hydrochloride were dissolved in a mixture of 20 ml methanol and 10 ml water. The solution was kept at 0° C., while 15 ml of an aqueous solution of 3.26 g (50 mmol) potassium cyanide were added dropwise. After stirring overnight at room temperature a crystalline solid had been formed, which was collected by filtration. The filtrate was treated with a mixture of water and ether. The organic layer was separated and the aqueous layer extracted with ether. The combined organic layers were dried over sodium sulfate and added to the solid material. The title hydrochloride precipitated after treating with a saturated ethereal solution of hydrogen chloride, and it was isolated by filtration and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291469B1
Source datasetuspto-grants-2001_09
ORD IDord-ca427e71e3154fee9cf6d6d1d46d4369
Source noteuspto-grants-2001_09