HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 1-Methyl-5-nitro-2-styrylimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Dimetridazole | HCID 3090 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 2-Methyl-5-nitroimidazole | HCID 12760 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Methyl-5-nitro-2-styrylimidazole | HCID 327486 | — |
Reaction Steps
The novel compounds coming within the scope of the generic formula, supra, are readily synthesized starting with commercially available 2-methyl-5-nitroimidazole. This starting compound is allowed to react with a suitable alkylating agent, such as dimethyl sulfate, in a suitable solvent, for example benzene, to yield the compound identified as 1,2-dimethyl-5-nitroimidazole. This latter compound is in turn allowed to react with benzaldehyde in the presence of a base, for example sodium ethoxide in absolute ethanol, to yield 1-methyl-5-nitro-2-styrylimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075222 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-e0063f8bb45a416e9c60f9be357de68b |
| Source note | uspto-grants-1978_02 |