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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915626Generated: November 1, 2026

Iodine → HCID 11845284, compound

https://huagongshe.com/reaction/915626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 10878008HCID 10878008—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 11845284HCID 1184528470%

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 (120 g;0.609 moles), sodium nitrite (96.6 g; 1.4 moles), iodine (31.2 g; 0.123 moles) and ethyl acetate (720 ml) were charged at room temperature and under inert gas. The mixture was heated under stirring at 40° C., then Oxistrong 15® (173.4 g) was added in 4 hours. At the end of the addition the reaction mixture was kept under stirring for 1 hour, then cooled at 20° C. Water (480 ml) was added and the mixture was kept under stirring for 1 hour. After filtration and wash of the panel with isopropyl acetate pre-cooled at 0° C. (2×120 ml) and then with water (150 ml), the solid was dried in oven under vacuum at 50° C. overnight obtaining 8-fluoro-3-nitro-2H-chromene-5-carboxylic acid amide (112.7 g; titre 91%; 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265251B2
Source datasetuspto-grants-2007_09
ORD IDord-b2ed860c7bb445bcba1e92a082950aaf
Source noteuspto-grants-2007_09