HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-Benzyl-4-hydroxy-3-isobutylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Benzyl-3-isobutylpiperidin-4-one | HCID 23003724 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Benzyl-4-hydroxy-3-isobutylpiperidine | HCID 23003697 | — |
Reaction Steps
Sodium borohydride (0.3 g, 9.0 mmole) was added to the stirred solution of 1-benzyl-3-isobutylpiperidin-4-one (1.0 g, 4.0 mmole) in methanol (10 ml) at 0-5° C. over a period of 5 min, and stirring was continued for 1 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water (20 ml) and extracted with ethyl acetate. The ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to furnish 1-benzyl-4-hydroxy-3-isobutylpiperidine as oil. Yield 0.63 g (54%), C16H25NO, m/z 248 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608078B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-4a2e4def4a9f45358c435662d61d1dd3 |
| Source note | uspto-grants-2003_08 |