HuagongsheHuagongshe Chemistry Print Report · For research reference only
Enantholactam → 1-Pent-4-enyl-azocan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Enantholactam | HCID 12657 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Pentene, 5-bromo- | HCID 70704 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Pent-4-enyl-azocan-2-one | HCID 21978547 | 94.4% |
Reaction Steps
To a stirred suspension of sodium hydride (0.9 g, 37.5 mmole) in dimethylformamide (50 mL) was added azocan-2-one (3.83 g, 30 mmole). The mixture was stirred at room temperature for 15 minutes, and then 5-bromo-1-pentene (5.03 g, 33.7 mmole) was added slowly. The reaction mixture was stirred at room temperature for 30 minutes, and then at 80° C. for 16 hours. The solvent was removed under reduced pressure and water was added to the residue. The mixture was extracted with ethyl ether, the organic phase was washed with water, dried (magnesium sulfate) and concentrated to give 1-pent-4-enyl-azocan-2-one (5.53 g,) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06667301B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-5cd3faaf42d842908600841ceb54943e |
| Source note | uspto-grants-2003_12 |