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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754987Generated: October 28, 2026

Ethyl isocyanatoacetate → HCID 66816429, compound

https://huagongshe.com/reaction/1754987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanatoacetateHCID 76283—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-2,6-xylidineHCID 90549—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 66816429HCID 6681642967.1%

Reaction Steps

Ethyl isocyanatoacetate (581 mg, 4.50 mmol) and N,N-diisopropylethylamine (426 mg, 1.65 mmol) were added to a solution of 4-bromo-2,6-dimethylaniline (600 mg, 3.00 mmol) in toluene (6 ml) with stirring in a nitrogen stream, and the mixture was heated with stirring at 120° C. After 30 minutes, the reaction solution was brought to room temperature, and the precipitate was collected by filtration, washed with toluene and then dried under reduced pressure. The resulting solid was suspended in toluene (6 ml). DBU (68.4 mg, 2.25 mmol) was added and the mixture was heated with stirring at 120° C. After 30 minutes, the reaction solution was brought to room temperature and diluted with ethyl acetate, and the organic layer was washed with a 1 N aqueous hydrochloric acid solution and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the magnesium sulfate was then removed by filtration. The filtrate was concentrated under reduced pressure. The residue was subjected to column chromatography (hexane-ethyl acetate) to give 3-(4-bromo-2,6-dimethyl-phenyl)-imidazolidine-2,4-dione (570 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-91a59b825f124942b0fb49266daad5df
Source noteuspto-grants-2015_10