HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminophenol → Methyl (3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl (3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl)acetate | HCID 4428325 | — |
Reaction Steps
A mixture of 76.4 g of 2-aminophenol and 68.6 g of maleic anhydride in 1 liter of methanol was stirred at room temperature. After addition of 100 ml of triethylamine, the yellow mass dissolved and the solution was heated for 7 hours at reflux temperature. The methanol was then removed by evaporation under reduced pressure, and the remaining oil was added to ice-water. The mixture was extracted with dichloromethane, and the organic extract was dried over sodium sulfate and evaporated. The remaining residue was crystallized from ethanol. In this way, 47.5 g of methyl (3-oxo-2,3-dihydro-4H-1,4-benzoxazin-2-yl)acetate were obtained as white crystals having a melting point of 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05474988 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-c850ca0036c84f29b30fdcba2953b59f |
| Source note | uspto-grants-1995_12 |