HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-[5-(2-Butylthioethyl) oxypentyl] azacycloheptane-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(Butylthio)ethanol | HCID 79241 | — |
| Reactant | 1-(5-Bromopentyl) azacycloheptane-2-one | HCID 14625932 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[5-(2-Butylthioethyl) oxypentyl] azacycloheptane-2-one | HCID 14625933 | 90.2% |
Reaction Steps
5.24 g of 1-(5-bromopentyl) azacycloheptane-2-one, 1.34 g of 2-(n-butylthio) ethanol, 2.24 g of powderly potassium hydroxide and 30 ml of dimethylsulfoxide were mixed together, agitated at room temperature for 10 hours, extracted with dichloromethane to obtain an extract. The thus obtained extract was washed with water, dried, freed from the solvent by distillation off at reduced pressure and then finally distilled to obtain 2.84 g of colorless 1-[5-(2-butylthioethyl) oxypentyl] azacycloheptane-2-one having the following appearance, column temperature and analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04882359 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-4dbf9d04999547dfa586da49d98c88b6 |
| Source note | uspto-grants-1989_11 |