HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288034Generated: October 31, 2026
HCID 23000816, compound → HCID 23000847, compound
https://huagongshe.com/reaction/2288034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23000816 | HCID 23000816 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23000847 | HCID 23000847 | 104.1% |
Reaction Steps
In 100 ml of ethanol, 4.68 g (20 mmol) of the resulting 1-benzyl-3-(1-hydroxyethyl)-4-piperidone were dissolved. To the resulting solution, 0.5 g of 5% palladium-carbon were added, followed by stirring at 60° C. for 8 hours under a hydrogen gas atmosphere. After the completion of the reaction, the palladium-carbon was removed by filtration through Celite. The solvent was then distilled off under reduced pressure, whereby 2.98 g of 3-(1-hydroxyethyl)-4-piperidone were obtained as a colorless oil in a quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06087379 |
|---|
| Source dataset | uspto-grants-2000_07 |
|---|
| ORD ID | ord-e62ac1cbf9f3428a9b2bf063d23c2348 |
|---|
| Source note | uspto-grants-2000_07 |
|---|