Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414637Generated: October 30, 2026

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

https://huagongshe.com/reaction/414637

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 1373129562.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Iron powder (36.42 g) was 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) was dropwise added, and the resultant mixture was heated at 60° to 80° C. under reflux for 3 hours. After removal of residue by filtration, the filtrate was extracted with ethyl acetate. The extract was washed with water and sodium bicarbonate solution, dried and concentrated to give 7-fluoro-2H-1,4-benzoxazin-3(4H)-one (6.82 g). m.p., 186.720 C. 1H-NMR (CDCl3 +DMSO-D6) δ ppm: 4.2 (1H, broad), 4.51 (2H, s), 6.5-7.0 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792605
Source datasetuspto-grants-1988_12
ORD IDord-ee869cf78138400f902e92f46f79bca9
Source noteuspto-grants-1988_12