HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255174Generated: October 29, 2026
Ethyl bromoacetate → 6-Nitro-2H-1,4-benzoxazin-3(4H)-one
https://huagongshe.com/reaction/2255174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-Amino-4-Nitrophenol | HCID 3613389 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Nitro-2H-1,4-benzoxazin-3(4H)-one | HCID 2763683 | 27% |
Reaction Steps
To a mixture of 10.6 g (182 mmol) of potassium fluoride and 55 ml of anhydrous dimethylformamide was added 7.76 ml (72 mmol) of ethyl bromoacetate and the reaction mixture was stirred at room temperature for 15 minutes. Then 10.79 g (70.0 mmol) of 2-amino-4-nitrophenol was added and the reaction mixture was heated to 55° C. for 6 hours. The reaction mixture was cooled slowly to room temperature, stirred for 12 hours and poured onto 300 ml ice. The solid which formed was filtered off, washed with water and dried (20-50 Torr, 50° C., 16 hrs). The resulting orange solid was taken up in 100 ml EtOAc and 100 ml H2O. The aqueous layer was extracted with EtOAc (2×100 ml). The organic layers were then combined and washed with water (3×150 ml) and 10% HCl and dried (MgSO4). The solvent was removed in vacuo and the resulting solid was recrystallized from ethylene dichloride to yield 3.6 g (27% yield) of 6-nitro-2H-1,4-benzoxazin-3(4H)-one as an orange solid, m.p. 221°-223° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05238908 |
|---|
| Source dataset | uspto-grants-1993_08 |
|---|
| ORD ID | ord-fb583f94978d469d828b2fe42af1d687 |
|---|
| Source note | uspto-grants-1993_08 |
|---|