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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13286Generated: October 25, 2026

1,4-Dioxane → 2-(2-Fluoro-5-nitrophenyl)pyridine

https://huagongshe.com/reaction/13286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
ReactantSodium BicarbonateHCID 516892—
Product2-(2-Fluoro-5-nitrophenyl)pyridineHCID 22285300—

Reaction Steps

0.55 g of Tetrakis-triphenylphosphine palladium was added to a 1,4-dioxane (20 ml) solution of 2.1 g of 3-bromo-4-fluoro-nitrobenzene and 2.3 g of 2-trimethyltin-pyridine, and the reaction liquid was heated overnight under reflux. Aqueous saturated sodium bicarbonate was added to the reaction liquid, and extracted with ethyl acetate. The organic layer was washed with water and saturated saline, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=7/1) to obtain the entitled compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-b06ca7ffde7348cc9499a39a52f86f8f
Source noteuspto-grants-2010_06