HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Ethyl-8-benzyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Oxa-3,8-diazaspiro(4.5)decan-2-one, 8-benzyl- | HCID 199815 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Ethyl-8-benzyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one | HCID 13016590 | — |
Reaction Steps
A mixture of 16.5 g 8-benzyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one, 6.6 g, 50% suspension of sodium hydride in mineral oil, 15 g ethyl iodide and 70 ml N,N-dimethylformamide is heated at 90° for one hour. The mixture is poured into 150 ml water and the resulting mixture acidified with 10 N hydrochloric acid. The mixture is extracted with two 100 ml portions of hexane. The aqueous layer is basified with sodium hydroxide and extracted with three 75 ml portions of dichloromethane. Removal of solvent in vacuum affords a residue which when crystallized from heptane gives 3-ethyl-8-benzyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one, mp 105°-106°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04255432 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-9e9fd3dfb19e4dd4a035093bee46bbdc |
| Source note | uspto-grants-1981_03 |