HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-(6-nitro-2H-benzo[b][1,4]oxazin-4(3H)-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-nitro-3,4-dihydro-2H-1,4-benzoxazine | HCID 7062225 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(6-nitro-2H-benzo[b][1,4]oxazin-4(3H)-yl)ethanone | HCID 57864714 | 90% |
Reaction Steps
Under vigorous stirring at room temperature, acetyl chloride (1.02 g, 13 mmol) was added dropwise to a mixture of 6-nitro-3,4-dihydro-2H-benzo[1,4]oxazine (1.8 g, 10 mmol) and NaHCO3 (7.14 g, 85 mmol) in CH2Cl2 (50 mL). After addition, the reaction was stirred for 1 h at this temperature. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was treated with Et2O:hexane (1:2, 50 mL) under stirring for 30 min and then filtered to give 4-acetyl-6-nitro-3,4-dihydro-2H-benzo[1,4]oxazine as a pale yellow solid (2 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829204B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7ccda5df6a2047b99cc019ca9cb59536 |
| Source note | uspto-grants-2014_09 |