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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441093Generated: November 1, 2026

Ethyl bromoacetate → 6-Nitro-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/1441093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium FluorideHCID 522689—
Reactant2-Amino-4-NitrophenolHCID 3613389—
SolventDimethylformamideHCID 6228—
Product6-Nitro-2H-1,4-benzoxazin-3(4H)-oneHCID 276368327%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05502027
Source datasetuspto-grants-1996_03
ORD IDord-84531887c3da43679e924ebd8b244bf3
Source noteuspto-grants-1996_03