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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654442Generated: October 26, 2026

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

https://huagongshe.com/reaction/1654442

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 Chemical Co., Inc., supra) (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 of 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 numberUS05407834
Source datasetuspto-grants-1995_04
ORD IDord-e9eb45a7ba054cfdad2ba32fbf3cd446
Source noteuspto-grants-1995_04