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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915625Generated: November 1, 2026

Potassium Iodide → HCID 11845284, compound

https://huagongshe.com/reaction/915625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantHCID 10878008HCID 10878008—
ReactantSodium NitriteHCID 23668193—
SolventEthyl AcetateHCID 8857—
ProductHCID 11845284HCID 1184528466%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265251B2
Source datasetuspto-grants-2007_09
ORD IDord-04a6b08253574b388d6eb9ace0c29283
Source noteuspto-grants-2007_09