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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915623Generated: November 1, 2026

Iodine → HCID 11845284, compound

https://huagongshe.com/reaction/915623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium PyrosulfiteHCID 656671—
ReactantHCID 10878008HCID 10878008—
ReactantSodium NitriteHCID 23668193—
SolventTolueneHCID 1140—
ProductHCID 11845284HCID 1184528474%

Reaction Conditions

Temperature50 °C

Reaction Steps

Into a reactor, equipped with a mechanic stirrer and a reflux condenser, 8-fluoro-2H-chromene-5-carboxylic acid amide (3.1 g; 15 mmoles), sodium nitrite (3.1 g; 45 mmoles) and toluene (30 ml) were charged at room temperature and under inert gas. The mixture was heated under stirring at 50° C., then iodine (1.9 g; 7.5 mmoles) and, slowly in 4 hours, Oxistrong 15® (3.7 ml) were added. At the end of the addition the reaction mixture was kept under stirring for a further hour, then cooled to 0° C. A 20% solution of sodium metabisulphite (about 15 ml) was added and the mixture was kept under stirring for 1 hour. After filtration the solid was washed with water (2×10 ml) and with toluene (10 ml) and dried in oven under vacuum at 50° C. overnight obtaining 8-fluoro-3-nitro-2H-chromene-5-carboxylic acid amide (3.4 g; titre 78%; 74% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265251B2
Source datasetuspto-grants-2007_09
ORD IDord-07240833fb11448cbb80392799edcf9d
Source noteuspto-grants-2007_09