HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466260Generated: October 25, 2026
Hydrochloric Acid → 1-(4-Hydroxypiperidin-1-yl)cyclohexane-1-carbonitrile
https://huagongshe.com/reaction/466260
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1-Hydroxypiperidine | HCID 20935 | — |
| Product | 1-(4-Hydroxypiperidin-1-yl)cyclohexane-1-carbonitrile | HCID 10058904 | — |
Reaction Steps
4 hydroxypiperidine (Aldrich Chemical Co., Inc., supra) (5q) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155212 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-a4eb416b22e64863aba5506a62cab93e |
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| Source note | uspto-grants-1992_10 |
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