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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335860Generated: October 30, 2026

Trifluoroacetic anhydride → 8-bromo-4-nitro-10-oxo-10H-chromeno[3,2-b]pyridine 1-oxide

https://huagongshe.com/reaction/335860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantCarbamide PeroxideHCID 31294—
Reactant8-bromo-4-nitro-10H-chromeno[3,2-b]pyridin-10-oneHCID 67383249—
SolventDichloromethaneHCID 6344—
Product8-bromo-4-nitro-10-oxo-10H-chromeno[3,2-b]pyridine 1-oxideHCID 67382950—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of urea hydrogen peroxide (58.6 mg, 0.623 mmol) in 5 mL of CH2Cl2 at 0° C. was added dropwise trifluoroacetic anhydride (87 μL, 0.623 mmol). After stirring for 5 min at 0° C., a solution of 8-bromo-4-nitro-10H-chromeno[3,2-b]pyridin-10-one (80 mg, 0.249 mmol) in CH2Cl2 (5 mL) was added and the resulting reaction was stirred at rt for 1.5 h. The mixture was carefully quenched with saturated NaHCO3 and extracted with ethyl acetate (5×5 mL). The combined organics were dried over sodium sulfate, filtered and evaporated to dryness. Purification of the crude residue by column chromatography (CH2Cl2 to CH2Cl2/EA=10:1 to 5:1) gave 8-bromo-4-nitro-10-oxo-10H-chromeno[3,2-b]pyridine 1-oxide as an light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-0e469631d9bc42c084273d0099534bab
Source noteuspto-grants-2014_11