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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420101Generated: October 29, 2026

4-Fluoroiodobenzene → HCID 178476783, compound

https://huagongshe.com/reaction/420101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroiodobenzeneHCID 9605—
Reactant(3-Aminopropyl)triethoxysilaneHCID 13521—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 178527020HCID 178527020—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
ProductHCID 178476783HCID 17847678348%

Reaction Steps

To a degassed mixture of 4-fluoro-1-iodo-benzene (25.0 g, 112.6 mmol), anilinium hypophosphite (21.5 g, 135.1 mmol) and 3-aminopropyl triethoxysilane (24.9 g, 135.1 mmol) in anhydrous acetonitrile (750 mL) were added palladium acetate (560 mg, 2.48 mmol) and 1,3-bis(diphenylphosphino)propane (1.02 g, 2.48 mmol). The mixture was heated under reflux overnight, then cooled down to room temperature, and the volatiles were removed in vacuo. The residue was diluted with ethyl acetate and hydrochloric acid (1M) and partitioned. The aqueous layer was further extracted with ethyl acetate and the combined extracts were washed with aqueous sodium hydrogen carbonate and brine. The volatiles were removed in vacuo, then the residue was purified by column chromatography using 50 to 100% ethyl acetate in petroleum ether, affording compound AZ2 (10.1 g) as a dark orange oil in 48% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093379B2
Source datasetuspto-grants-2012_01
ORD IDord-2d630c8e0f7640378662367f01daf97d
Source noteuspto-grants-2012_01