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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973146Generated: October 30, 2026

Ethyl bromoacetate → Dimethyl 2,2'-(2,2-dimethyl-4,5-dioxoimidazolidine-1,3-diyl)diacetate

https://huagongshe.com/reaction/973146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant2,2-Dimethylimidazolidine-4,5-dioneHCID 3015721—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductDimethyl 2,2'-(2,2-dimethyl-4,5-dioxoimidazolidine-1,3-diyl)diacetateHCID 2140146828.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 12.8 g (0.1 mole) of 2,2-dimethylimidazolidine-4,5-dione in 70 ml of dimethyl formamide is slowly added dropwise, with stirring, at 20°-30° C to a suspension of 4.8 g (0.2 mole) of sodium hydride in 60 ml of dimethyl formamide. When the uptake of hydrogen has ceased, a solution of 33.4 g (0.2 mole) of bromacetic acid ethyl ester in 30 ml of dimethylformamide is added dropwise at 40°-50° C. After it has been stirred for 1 hour at 80° C, the reaction mixture is evaporated to dryness in vacuo. The residue is washed with ether and taken up in chloroform. The insoluble potassium bromide is filtered off and the chloroform solution evaporated. The residue is recrystallised from n-butanol to yield 7.8 g of colourless crystals with a melting point of 129°-130° C. The infra-red and nuclear magnetic resonance spectra confirm the presumed structure and the results of the elemental analysis are:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055570
Source datasetuspto-grants-1977_10
ORD IDord-234630777c764f528b667939b5f309be
Source noteuspto-grants-1977_10