HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-Benzyl-3-ethyl-4-hydroxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Benzyl-3-ethylpiperidin-4-one | HCID 6490960 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Benzyl-3-ethyl-4-hydroxypiperidine | HCID 23003710 | — |
Reaction Steps
Sodium borohydride (0.456 g, 12.0 mmole) was added to the stirred solution of 1-benzyl-3-ethyl piperidin-4-one (5.4 g, 24.0 mmole) in methanol (25 ml) at 0-5° C. over a period of 15 min, and stirring was continued for 30 min at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water (25 ml) and extracted with ethyl acetate (2×100 ml). The extract was dried (sodium sulphate) and concentrated to dryness to furnish 1-benzyl-3-ethyl-4-hydroxypiperidine product as oil, which was used as such in the next step. Yield 5.2 g (96%), C14H21NO, m/z 220 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608078B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-0f81e856b6d2401bb89591ea33087e70 |
| Source note | uspto-grants-2003_08 |