HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Azaspiro[4.6]undecan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23336701 | HCID 23336701 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Azaspiro[4.6]undecan-3-one | HCID 23336699 | — |
Reaction Steps
38 g. N-acetyl-3-oxo-2-azaspiro[4,6]undecane are heated to 60° C. for 6 hours in a solution of 40 g. potassium carbonate in 400 ml. 80% aqueous ethanol. The reaction mixture is then acidified with dilute hydrochloric acid, the ethanol is stripped off in a vacuum and the aqueous residue is extracted with methylene chloride. The residue obtained after evaporation of the solvent gives, upon vacuum distillation, 3-oxo-2-azaspiro[4,6]undecane in the form of a colourless syrup; b.p. 125°-135° C./10-3 mm.Hg. After crystallisation from diisopropyl ether, the compound melts at 70°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04228179 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-0555c20d69ff4e97a50ff66a54f7965e |
| Source note | uspto-grants-1980_10 |