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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960183Generated: October 30, 2026

(3-Aminopropyl)triethoxysilane → HCID 178476782, compound

https://huagongshe.com/reaction/1960183

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 refluxed for 32 hrs. After cooling down to room temperature, the reaction mixture was diluted with ethyl acetate and hydrochloric acid (1M), and partitioned. The aqueous layer was further extracted with ethyl acetate. The combined extracts were washed sequentially with aqueous sodium hydrogen carbonate and brine, dried over magnesium sulfate, and concentration in vacuo. The resulting 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. 1H NMR (CDCl3, 400 MHz): δ (ppm) 1.35-1.43 (m, 3H), 4.12-4.27 (m, 2H), 7.63 (d, J=570.8 Hz, 1H), 7.75-7.80 (m, 2H), 7.90-7.94 (m, 2H); 31P NMR (CDCl3, 161.8 MHz): δ (ppm) 22.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410313B2
Source datasetuspto-grants-2013_04
ORD IDord-af1410c2e92d4171a42c15b1a17697c4
Source noteuspto-grants-2013_04