HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetyl-4-piperidone → 1-(4-Hydroxypiperidin-1-yl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetyl-4-piperidone | HCID 122563 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-(4-Hydroxypiperidin-1-yl)ethan-1-one | HCID 10749291 | 100% |
Reaction Steps
To a cooled (0° C.) mixture of NaBH4 (2.15 g, 0.057 mol) and isopropanol (70 mL) was added N-acetyl-4-piperidone (8.00 g, 0.057 mol). The mixture was allowed to warm to room temperature and stirred for 16 hours. CO2 was bubbled into the reaction mixture, EtOAc (120 mL) was added, and the precipitate was removed by filtration. The filtrate was concentrated to give 8.0 g (100%) of N-acetyl-4-hydroxypiperidine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254689 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-270cea07e37042d5a8c0128d7e1badc1 |
| Source note | uspto-grants-1993_10 |