HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929439Generated: October 30, 2026
Potassium Fluoride → HCID 66789964, compound
https://huagongshe.com/reaction/1929439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Acetic acid, 2-bromo-2-fluoro-, ethyl ester | HCID 2733407 | — |
| Reactant | 2-Amino-5-Nitrophenol | HCID 4984721 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66789964 | HCID 66789964 | 41.8% |
Reaction Steps
To a suspension of 2-amino-5-nitrophenol (1.98 g) and potassium fluoride (2.24 g) in N,N-dimethylformamide (40 mL) was added ethyl bromofluoroacetate (2.85 g), and the mixture was stirred at 60° C. for 44 hours. After cooling, the reaction mixture was diluted with ethyl acetate, and the mixture was washed successively with water and brine. The organic layer was dried over magnesium sulfate and concentrated in vacuo. The resultant residue was purified by column chromatography on silica gel (solvent; n-hexane/ethyl acetate=19/1→1/1) and triturated with n-hexane/diisopropylether to give 2-fluoro-7-nitro-2H-1,4-benzoxazin-3(4H)-one (1.14 g) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188073B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-5fa662eb2394424e81f38426beea1b37 |
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| Source note | uspto-grants-2012_05 |
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