HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420101Generated: October 29, 2026
4-Fluoroiodobenzene → HCID 178476783, compound
https://huagongshe.com/reaction/420101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluoroiodobenzene | HCID 9605 | — |
| Reactant | (3-Aminopropyl)triethoxysilane | HCID 13521 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | HCID 178527020 | HCID 178527020 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178476783 | HCID 178476783 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093379B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-2d630c8e0f7640378662367f01daf97d |
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| Source note | uspto-grants-2012_01 |
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