HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Aminomethyl)cyclohexan-1-ol → 1-Oxa-3-azaspiro(4.5)decan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Aminomethyl)cyclohexan-1-ol | HCID 77614 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Oxa-3-azaspiro(4.5)decan-2-one | HCID 349043 | — |
Reaction Steps
0.65 g (5.0 mmol) of 1-(aminomethyl)-cyclohexanol, 1.2 g (5.5 mmol) di-tert.-butyldicarbonate ((Boc)2O) and 0.611 g 4-dimethylaminopyridine were dissolved in 50 ml acetonitrile and agitated overnight at room temperature. The mixture was then fully turned over, the residue was dissolved in 20 ml acetic acid and again turned over. The residue was taken up in 25 ml 1 M hydrochloric acid and extracted with 50 ml toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07282515B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-7ac8cd96d6e54722932bd77cad796e30 |
| Source note | uspto-grants-2007_10 |