HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178437617, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Aminobutyric acid methyl ester | HCID 151013 | — |
| Reactant | HCID 178468373 | HCID 178468373 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178437617 | HCID 178437617 | 62% |
Reaction Steps
To 4.99 g (0.039 moles) of 3-oximino-2,4-pentanedione dissolved in acetonitrile (40 ml) was added 4.59 ml (0.039 moles) of methyl 2-aminobutyrate. After stirring for two hours at room temperature, then at reflux for 2.5 h, the reaction mixture was cooled and treated with 15 ml of ethanol and 15 ml of 10% aqueous sodium hydroxide. The resulting mixture was refluxed for 3.8 h, cooled, then extracted with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate, then concentrated in vacuo to give 0.024 moles (62% yield) of 5-acetyl-2-ethyl-4-methylimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04395547 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-c351ba9af31c4b829a8d17528942ed03 |
| Source note | uspto-grants-1983_07 |