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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl iminodiacetate | HCID 80502 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178513139 | HCID 178513139 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one | HCID 136040605 | 27.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677322 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-42be6173687f454a955d4788289f00de |
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| Source note | uspto-grants-1997_10 |
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