HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13755489, compound → 1-(4-Oxocyclohexyl)imidazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13755489 | HCID 13755489 | — |
| Reactant | Potassium hypochlorite | HCID 23665762 | — |
| Catalyst | Benzyltributylammonium chloride | HCID 159952 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-Oxocyclohexyl)imidazolidin-2-one | HCID 20223082 | — |
Reaction Steps
A mixture of 18.3 g of 1-(4-aminocyclohexyl)-2-imidazolidinone as a mixture of cis and trans isomers, 2.0 g of benzyltributylammonium chloride, 250 ml of ethyl acetate and 360 ml of an aqueous 10% potassium hypochlorite solution [according to methodology as described by C. A. Meyers, J. Org. Chem. 26, 1046 (1961)] is stirred at room temperature for 11/2 hours. The organic layer is separated and the aqueous layer is extracted with ethyl acetate. The pooled organic phases are washed with water, sodium bicarbonate solution and dilute hydrochloric acid, then dried and evaporated to dryness to yield 1-(4-oxocyclohexyl)-2-imidazolidinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634713 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-9fd8a531d3e44da2bc425bc004f22739 |
| Source note | uspto-grants-1987_01 |