HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255179Generated: October 30, 2026
Methyl 2,4-dinitro-5-fluorophenoxyacetate → 7-Fluoro-6-amino-2H-1,4-benzoxazin-3(4H)-one
https://huagongshe.com/reaction/2255179
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 2,4-dinitro-5-fluorophenoxyacetate | HCID 14423669 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Fluoro-6-amino-2H-1,4-benzoxazin-3(4H)-one | HCID 10313389 | 60% |
Reaction Steps
To a suspension of 12.2 g (0.22 mol) of iron powder in 100 ml of 5% aqueous acetic acid was added dropwise a solution of 10.0 g (36.5 mmol) of methyl 2,4-dinitro-5-fluorophenoxyacetate in 100 ml of EtOAc and 100 ml of glacial acetic acid. The reaction mixture was stirred at room temperature for 18 hours. The iron was removed by suction filtration through a small pad of Celite® and the filter pad was rinsed with 50 ml of EtOAc. The filtrate was transferred to a separatory funnel and the phases were separated. The aqueous layer was extracted with EtOAc (3×50 ml) and the combined organic phases were washed with sodium bicarbonate (2×50 ml), dried over Na2SO4 and filtered. The solvent was removed from the filtrate in vacuo to yield 3.9 g (60% yield) of 6-amino-7-fluoro-2H-1,4-benzoxazin-3(4H)-one as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05238908 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-581ebe0867804e2d9a5610259bf7c871 |
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| Source note | uspto-grants-1993_08 |
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