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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413741Generated: October 31, 2026

Ethanol → Ethyl 2,2-dimethyl-5-oxo-1-imidazolidineacetate

https://huagongshe.com/reaction/2413741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium 2,2-dimethyl-5-oxo-1-imidazolidineacetateHCID 23686064—
ProductEthyl 2,2-dimethyl-5-oxo-1-imidazolidineacetateHCID 53986652—

Reaction Conditions

Temperature0 °C

Reaction Steps

(1) To an ice cold solution of thionyl chloride (5 ml) in dry ethanol (50 ml) a solution of sodium 2,2-dimethyl-5-oxo-1-imidazolidineacetate (4 g) in dry ethanol (50 ml) was added dropwise. The mixture was stirred at 0° C. for 1 hour, then at room temperature overnight. After evaporation under reduced pressure, the residue was taken up with a saturated solution of sodium hydrogen carbonate and extracted with 3×100 ml of dichloromethane. The organic layer was dried and evaporated, to yield ethyl 2,2-dimethyl-5-oxo-1-imidazolidineacetate (2.57 g) as a colorless oil (Rf. 0.49, methanol/acetone 1:1; silica gel plates). Oxalate salt m.p. 109°-113° C. (ethanol/diethyl ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719222
Source datasetuspto-grants-1988_01
ORD IDord-f470cbdd7c894ceca85f50fb2cae9556
Source noteuspto-grants-1988_01