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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420098Generated: October 25, 2026

(3-Aminopropyl)triethoxysilane → HCID 178476782, compound

https://huagongshe.com/reaction/420098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Aminopropyl)triethoxysilaneHCID 13521—
ReactantBenzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 178527020HCID 178527020—
Catalystpalladium(II) acetateHCID 167845—
SolventHydrochloric AcidHCID 313—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 178476782HCID 17847678228%

Reaction Steps

To a degassed solution of 4-iodobenzotrifluoride (4.70 g, 17.2 mmol), anilinium hypophosphite (3.51 g, 22.1 mmol), and 3-aminopropyl triethoxysilane (4.88 g, 22.1 mmol) in anhydrous acetonitrile (110 mL) were added palladium acetate (82.5 mg, 0.367 mmol, 2 mol %) and 1,3-bis(diphenylphosphino)propane (167 mg, 0.404 mol, 2.2 mol %). The mixture was heated under reflux for 32 hrs, then cooled down to room temperature, diluted with ethyl acetate and hydrochloric acid (IM) and partitioned. The aqueous layer was further extracted with ethyl acetate, and the combined extracts were washed with aqueous sodium hydrogen carbonate and brine and dried over magnesium sulfate. The solvent was removed in vacuo and the residue was purified by column chromatography using 25 to 100% ethyl acetate in petroleum ether. Further purification by distillation afforded compound AZ1 (1.14 g) in 28% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093379B2
Source datasetuspto-grants-2012_01
ORD IDord-5b6d117b552d4e7c892d8dde9ed0d3c0
Source noteuspto-grants-2012_01