HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3,5-Diethyl-3-methyl-1-(phenylmethyl)-4-piperidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Benzyl-3-methyl-4-piperidone | HCID 560965 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,5-Diethyl-3-methyl-1-(phenylmethyl)-4-piperidinone | HCID 22278878 | — |
Reaction Steps
1-Benzyl-3-methyl-piperidin-4-one (50 g, 246 mmole) was added to the stirred suspension of sodium hydride (12.0 g, 300.0 mmole) in tetrahydrofuran (500 ml) at ambient temperature and stirring was continued for 1 hr. Ethyl iodide (42.5 ml, 520.0 mmole) in dry tetrahydrofuran (100 ml) was added it at 0-5° C. The resulting mixture stirred at room temperature for 18 hr, water (100 ml) and ethyl acetate (800 ml) were added respectively. Organic layer was separated, dried (Na2SO4) and concentrated to give crude product, which was purified through column chromatography. Elute from 5% ethyl acetate in hexane afforded 1-benzyl-3,5-diethyl-3-methylpiperidin-4-one. Yield 12.0 g (19%), C17H25NO, m/z 260 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608078B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-cd8fac6196d04a7a999cf56a9f06cb86 |
| Source note | uspto-grants-2003_08 |