HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 5-Benzoyl-2-ethyl-4-methylimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Aminobutyric acid methyl ester | HCID 151013 | — |
| Reactant | 5-Acetyl-2-ethyl-4-phenylimidazole | HCID 20454139 | — |
| Reactant | 2-hydroxyimino-1-phenylbutane-1,3-dione | HCID 178468376 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 5-Benzoyl-2-ethyl-4-methylimidazole | HCID 178437626 | 42% |
Reaction Steps
An acetonitrile solution (15 ml) of 2-oximino-1-phenyl-1,3-butanedione (1.38 g, 7.22 mmoles) and methyl 2-aminobutyrate (0.85 ml, 7.22 mmol) was refluxed under nitrogen for 26.4 h. After concentrating the cooled reaction mixture, the residue was dissolved in 10 ml of ethanol and 20 ml of 10% aqueous sodium hydroxide. This mixture was refluxed 4.9 h, cooled, then extracted with ethyl acetate. Removal of the solvent in vacuo gave 0.65 g (42% yield) of 5-benzoyl-2-ethyl-4-methylimidazole and 5-acetyl-2-ethyl-4-phenylimidazole (86:14 respectively).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04459413 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-09375081d0dd468ea6ac6b1b1243ea5d |
| Source note | uspto-grants-1984_07 |