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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489134Generated: October 29, 2026

Diethyl iminodiacetate → 2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one

https://huagongshe.com/reaction/1489134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl iminodiacetateHCID 80502—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178513139HCID 178513139—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-oneHCID 13604060527.1%

Reaction Steps

To a methanol solution of sodium methoxide prepared by dissolving 2.30 g of metal sodium in 150 ml of methanol was added 5.70 g of benzylideneaminoguanidine, and, after stirring the mixture for one hour at room temperature, 11.35 g of iminodiacetic acid diethyl ester was added thereto, followed by refluxing under heating for 17 hours. After cooling the reaction mixture, water and chloroform were added thereto to distribute the mixture between aqueous and organic layers and, then, the aqueous layer was extracted three times with chloroform. The organic layer was combined with the extract. After drying over anhydrous magnesium sulfate, the mixture was concentrated under reduced pressure, and the residue was charged on silica gel column chromatography, followed by elution with a mixed solvent of chloroform and methanol (100:1 (v/v)). Thus 2.61 g of 2-benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677322
Source datasetuspto-grants-1997_10
ORD IDord-42be6173687f454a955d4788289f00de
Source noteuspto-grants-1997_10