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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030959Generated: October 31, 2026

Ethyl 2-(5-fluoro-2-nitrophenoxy)acetate → 7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one

https://huagongshe.com/reaction/1030959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(5-fluoro-2-nitrophenoxy)acetateHCID 13752803—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 13731295—

Reaction Conditions

Temperature80 °C

Reaction Steps

Iron powder (36.42 g) is suspended in 5% aqueous acetic acid (69 ml) and heated to 80° C. To the suspension, a solution of ethyl 5-fluoro-2-nitrophenoxyacetate (15.86 g) in acetic acid (65 ml) and ethyl acetate (65 ml) is dropwise added, and the resulting mixture is heated at 60° to 80° C. under reflux for 3 hours. After removal of residue by filtration, the filtrate is extracted with ethyl acetate. The extract is washed with water and sodium bicarbonate solution, dried and concentrated to give 7-fluoro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05108488
Source datasetuspto-grants-1992_04
ORD IDord-47a21b85ac1c4cbebd79e156d12889f4
Source noteuspto-grants-1992_04