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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359308Generated: October 25, 2026

Dimethylformamide → 2-Ethylhexyl 4-(3,4-dimethoxyphenylmethylene)-2,5-dioxo-1-imidazolidinepropionate

https://huagongshe.com/reaction/359308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-Ethylhexyl acrylateHCID 7636—
ReactantPotassium HydroxideHCID 14797—
Reactant5-[(3,4-Dimethoxyphenyl)methylidene]imidazolidine-2,4-dioneHCID 165798—
SolventWaterHCID 962—
Product2-Ethylhexyl 4-(3,4-dimethoxyphenylmethylene)-2,5-dioxo-1-imidazolidinepropionateHCID 5440952177.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

20 g (80.6 mmol) of 5-(3,4-dimethoxybenzylidene)-hydantoin, 17.8 g (96 mmol) of 2-ethylhexyl acrylate and 0.90 g (1.6 mmol) of potassium hydroxide were added to 150 ml of dimethylformamide, and the mixture was stirred at 110° C. for 2 hours. After cooling, the reaction solution was added with 200 ml of water and extracted with 500 ml of ethyl acetate. The extract was dried with sodium sulfate and then the solvent was distilled off under reduced pressure. The residue was recrystallized with toluene-n-hexane (1:1) and the precipitated crystals were dried to obtain 27.1 g of 2-ethylhexyl 4-(3,4-dimethoxyphenylmethylene)-2,5-dioxo-1-imidazolidinepropionate (yield: 77.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05000945
Source datasetuspto-grants-1991_03
ORD IDord-fe84fff7d4cd4b6ca592861b3f59b72a
Source noteuspto-grants-1991_03