HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587740Generated: October 31, 2026
1,3-Dimethyl-2-imidazolidinone → HCID 136331481, compound
https://huagongshe.com/reaction/1587740
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Reactant | N-nitroimidazolidin-2-imine | HCID 135413413 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 136331481 | HCID 136331481 | 53% |
Reaction Steps
A mixture of 5.0 g of p-aminoacetophenone. 6.6 g of ethyl orthoformate, 5 ml of 1,3-dimethyl-2-imidazolidinone and 0.03 g of concentrated sulfuric acid was placed in a reactor equipped with Dean's stark tube and agitated at 140° C. for about 10 minutes, followed by further addition of 5.8 g of nitroiminoimidazolidine and agitation at 160° C. for 1 hour. The reaction mixture was poured into 200 ml of a saturated saline solution, to which 150 ml of ethyl acetate was added. The resultant crystals were collected by filtration, and dried to give 5.4 g of 1-(4-methylcarbonyl-phenyliminomethyl)-2-nitroiminoimidazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05219868 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-892d5c7f0fc544b9b232cf07c8a14e7f |
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| Source note | uspto-grants-1993_06 |
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