HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-(3,4-Dihydroquinoxalin-1(2h)-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,2,3,4-Tetrahydroquinoxaline | HCID 77028 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(3,4-Dihydroquinoxalin-1(2h)-yl)ethanone | HCID 241507 | — |
Reaction Steps
To a solution of 1,2,3,4-tetrahydroquinoxaline obtained in Reference Example 26 (360 mg) in ethanol (10 ml), acetic anhydride (254 μl) was added dropwise under ice cooling and stirred at room temperature for 10 minutes. The reaction mixture was diluted with 1M aqueous sodium hydroxide (10 ml) and extracted with chloroform. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The desiccant was filtered off and the solvent was distilled off under reduced pressure to give the titled compound, i.e., 1-acetyl-1,2,3,4-tetrahydroquinoxaline (494 mg) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222417B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-a3fe6206b0324603b0201b52ce20cac5 |
| Source note | uspto-grants-2012_07 |