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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035313Generated: October 25, 2026

Potassium Cyanide → 1-Ethoxy-4-hydroxy-piperidine-4-carbonitrile

https://huagongshe.com/reaction/2035313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantSodium BisulfiteHCID 23665763—
Reactant1-Ethoxypiperidin-4-oneHCID 57096529—
SolventWaterHCID 962—
Product1-Ethoxy-4-hydroxy-piperidine-4-carbonitrileHCID 86663301—

Reaction Steps

A solution of sodium bisulfite (10.7 g, 103 mmol) in 10 ml of water was cooled in an ice bath. Then, 1-ethoxy-piperidin-4-one (12.3 g, 86 mmol, prepared according to J. Org. Chem. 1961, 26, 1867-74) was added dropwise. After the addition, the mixture was stirred for another 30 min. A solution of potassium cyanide (8.4 g, 129 mmol) in 10 ml of water was added slowly, the reaction mixture was warmed up to room temperature and left stirring for 24 hours. The mixture was thoroughly extracted with ethyl acetate (4×30 ml) and the combined organic layers were washed twice with brine (2×30 ml) and dried over sodium sulfate. After filtration and concentration under vacuum, the residue was purified by column chromatography on silica gel. Yield: 13.2 g of 1-ethoxy-4-hydroxy-piperidine-4-carbonitrile (title compound P4.9) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08574607B2
Source datasetuspto-grants-2013_11
ORD IDord-e052a243bc8b449595334c5c76e1f5de
Source noteuspto-grants-2013_11