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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543461Generated: October 26, 2026

Potassium Cyanide → 4-Cyano-4-(piperidin-1-yl)cyclohexyl benzoate

https://huagongshe.com/reaction/543461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant4-(Benzoyloxy)cyclohexanoneHCID 242677—
ReactantPiperidine, hydrochloride (1:1)HCID 2723721—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Cyano-4-(piperidin-1-yl)cyclohexyl benzoateHCID 1330675575%

Reaction Steps

4-Benzoyloxycyclohexanone (13.5 g, 62 mmoles), piperidine hydrochloride (8.1 g, 67 mmoles) and potassium cyanide (4.25 g, 65 mmoles) were dissolved in 60 ml of 95% ethanol and 60 ml of water. The mixture was stirred at room temperature for 16 hours (overnight). The resulting solid material was collected by filtration. The filtrate was diluted with 100 ml of water and the solution was extracted with ether. Concentration of the ethereal solution gave more solid material. The combined solid material was recrystallized from 90% ethanol to give 14.5 g of white crystalline solid (mp: 165°-171° C.) in 75% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04446065
Source datasetuspto-grants-1984_05
ORD IDord-3f2b1cd117874e938a46920dd877daa0
Source noteuspto-grants-1984_05