HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080609Generated: November 1, 2026
N,N'-Dimethylurea → 1,3-Dimethylimidazolidine-2,4-dione
https://huagongshe.com/reaction/2080609
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Dimethylurea | HCID 7293 | — |
| Reactant | Glyoxal | HCID 7860 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Dimethylimidazolidine-2,4-dione | HCID 123410 | 85% |
Reaction Steps
In a 1000 ml glass vessel equipped with a stirrer, thermometer, a dropping funnel and a distillation unit was charged 290 g (2.0 mol) of 40 wt % aqueous glyoxal solution. And then, triethylamine is added thereto to prepare a basic mixed solution (At this time, the solution had a pH of 9). To the mixed solution was gradually added dropwise a solution comprising 176 g (2.0 mol) of 1,3-dimethylurea and 176 ml of water while maintaining a liquid temperature to 25 to 35° C. After stirring the solution at room temperature for 3 hours, the mixture was reacted by elevating the temperature to 200° C. over 2 hours while removing triethylamine and water under normal pressure by distillation. After completion of the reaction, the obtained reaction mixture was distilled under reduced pressure (105 to 107° C./0.67 to 1.33 kPa) to obtain 217 g (Isolation yield; 85%) of 1,3-dimethylimidazolidin-2,4-dione as a pale yellowish liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932400B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-8ba7c2a8b0944e0089f35470fd41284f |
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| Source note | uspto-grants-2011_04 |
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