HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915625Generated: November 1, 2026
Potassium Iodide → HCID 11845284, compound
https://huagongshe.com/reaction/915625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | HCID 10878008 | HCID 10878008 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11845284 | HCID 11845284 | 66% |
Reaction Steps
Into a reactor, equipped with a mechanic stirrer and a reflux condenser, 8-fluoro-2H-chromene-5-carboxylic acid amide (2 g; 10 mmoles), sodium nitrite (1.4 g; 20 mmoles), potassium iodide (0.33 g; 2 mmoles) and ethyl acetate (20 ml) were charged at room temperature and under inert gas. The mixture was heated at 40° C., then Oxistrong 15® (4 ml) was added in 4 hours. At the end of the addition the reaction mixture was kept under stirring for 1.5 hours, then cooled at 20° C. and diluted with ethyl acetate up to complete dissolution (about 150 ml). After washing with a 20% sodium metabisulphite solution, the phases were separated. The organic phase was washed with a saturated sodium chloride solution, dried and the solvent was removed under reduced pressure, obtaining 8-fluoro-3-nitro-2H-chromene-5-carboxylic acid amide (1.8 g; titre 88%; 66% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07265251B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-04a6b08253574b388d6eb9ace0c29283 |
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| Source note | uspto-grants-2007_09 |
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