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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979903Generated: October 29, 2026

HCID 13755489, compound → 1-(4-Oxocyclohexyl)imidazolidin-2-one

https://huagongshe.com/reaction/979903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13755489HCID 13755489—
ReactantPotassium hypochloriteHCID 23665762—
CatalystBenzyltributylammonium chlorideHCID 159952—
SolventEthyl AcetateHCID 8857—
Product1-(4-Oxocyclohexyl)imidazolidin-2-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04634713
Source datasetuspto-grants-1987_01
ORD IDord-9fd8a531d3e44da2bc425bc004f22739
Source noteuspto-grants-1987_01