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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335861Generated: October 30, 2026

Phosphorus oxychloride → 8-bromo-2-chloro-4-nitro-10H-chromeno[3,2-b]pyridin-10-one

https://huagongshe.com/reaction/335861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant8-bromo-4-nitro-10-oxo-10H-chromeno[3,2-b]pyridine 1-oxideHCID 67382950—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product8-bromo-2-chloro-4-nitro-10H-chromeno[3,2-b]pyridin-10-oneHCID 86658470—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 8-bromo-4-nitro-10-oxo-10H-chromeno[3,2-b]pyridine 1-oxide (90 mg, 0.267 mmol) in 1 mL of dry DMF was added dropwise to a solution of phosphorus oxychloride (44.0 μL, 0.481 mmol) in 0.2 mL of DMF and 0.5 mL of toluene at 0° C. After stirring at 0° C. for 0.5 h, the reaction was 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=100:3) gave 8-bromo-2-chloro-4-nitro-10H-chromeno[3,2-b]pyridin-10-one as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-a82393c7c51745938b7ea0caf5f0bd70
Source noteuspto-grants-2014_11