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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588220Generated: October 26, 2026

Hydrochloric Acid → 1-(4-Hydroxypiperidin-1-yl)cyclohexane-1-carbonitrile

https://huagongshe.com/reaction/1588220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyclohexanoneHCID 7967—
ReactantPotassium CyanideHCID 9032—
ReactantPiperidin-4-olHCID 79341—
SolventWaterHCID 962—
Product1-(4-Hydroxypiperidin-1-yl)cyclohexane-1-carbonitrileHCID 10058904—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Hydroxypiperidine (Aldrich) (5 g) was dissolved in distilled water (14 ml), cooled to 0° C. and the pH was adjusted to between 4 and 5 by addition of concentrated hydrochloric acid and 4-hydroxypiperidine. After warming to room temperature, 5.2 ml cyclohexanone and 3.3 g potassium cyanide in water (9 ml) were added sequentially. After 18 hours stirring at room temperature, the solid was filtered. The solid was dissolved in 100 ml methylene chloride, dried over Na2SO4, filtered and the solvent was removed in vacuo to yield pure 1-(1-cyanocyclohexyl)-4-hydroxypiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05221629
Source datasetuspto-grants-1993_06
ORD IDord-4c3ef08d1b6b472996e7165b75d14bd6
Source noteuspto-grants-1993_06