HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 1-(2,2-Dimethoxyethyl)-piperidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Chlorovaleryl chloride | HCID 74089 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 1-(2,2-Dimethoxyethyl)-piperidin-2-one | HCID 21978509 | 80.9% |
Reaction Steps
To a stirred mixture of aminoacetaldehyde dimethylacetal (0.74 g, 7 mmole) in ethyl acetate (20 mL) and 2M sodium carbonate (20 mL) was added 5-chlorovaleryl chloride (1.55 g, 10 mmole). The reaction mixture was stirred at ambient temperature for 1 hour. The aqueous layer was separated and extracted with ethyl acetate. The combined organic phase was washed with 1% hydrochloric acid and water, dried (magnesium sulfate), and concentrated. The oily residue was dissolved in tetrahydrofuran, and sodium hydride (60% in oil) (0.3 g, 7.5 mmole) was added. The reaction mixture was heated under reflux for 1.5 hours and filtered. The filtrate was concentrated to give 1-(2,2-dimethoxyethyl)-piperidin-2-one (1.06 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06667301B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-e308edd1728144d6a35735d92e39833f |
| Source note | uspto-grants-2003_12 |