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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 1-Ethoxypiperidin-4-one | HCID 57096529 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Ethoxy-4-hydroxy-piperidine-4-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08574607B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-e052a243bc8b449595334c5c76e1f5de |
|---|
| Source note | uspto-grants-2013_11 |
|---|