HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dimethyl-2-imidazolidinone → 1-Diethoxymethyl-2-nitroiminoimidazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Reactant | N-nitroimidazolidin-2-imine | HCID 135413413 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Diethoxymethyl-2-nitroiminoimidazolidine | HCID 136403419 | — |
Reaction Steps
A mixture of 25 g of 2-nitroiminoimidazolidine, 100 g of ethyl orthoformate and 25 ml of 1,3-dimethyl-2-imidazolidinone was heated under reflux for 3 hours. After cooling to room temperature, the mixture was poured into water, followed by extraction with ethyl acetate. After washing with water, the extract was dried with anhydrous magnesium sulfate, after which the solvent was distilled off under reduced pressure. The resultant crystals were sludged with ether to give 32 g of 1-diethoxymethyl-2-nitroiminoimidazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264584 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-6d6a20cb54b64732b2db00d40b533e37 |
| Source note | uspto-grants-1993_11 |