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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877309Generated: November 1, 2026

(3-Aminopropyl)triethoxysilane → HCID 178476784, compound

https://huagongshe.com/reaction/1877309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Aminopropyl)triethoxysilaneHCID 13521—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
Reactant1-Iodo-3,5-bis(trifluoromethyl)benzeneHCID 630970—
ReactantHCID 178527020HCID 178527020—
Catalystpalladium(II) acetateHCID 167845—
SolventHydrochloric AcidHCID 313—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 178476784HCID 17847678452%

Reaction Steps

To a degassed solution of 1-iodo-3,5-bistrifluoromethylbenzene (10.0 g, 29.4 mmol), anilinium hypophosphite (5.62 g, 35.3 mmol) and 3-aminopropyl triethoxysilane (7.81 g, 35.3 mmol) in anhydrous acetonitrile (200 mL) were added palladium acetate (132 mg, 0.588 mmol, 2 mol %) and 1,3-bis(diphenylphosphino)propane (267 mg, 0.647 mol, 2.2 mol %). The mixture was refluxed overnight. After cooling down to room temperature, the reaction mixture was diluted with ethyl acetate and hydrochloric acid (IM), and then partitioned. The aqueous layer was further extracted with ethyl acetate. The combined extracts were washed sequentially with aqueous sodium hydrogen carbonate and brine, and dried over sodium sulfate. The volatiles were removed in vacuo, and the residue was purified by column chromatography using 30 to 70% ethyl acetate in petroleum ether to afford compound AZ3 (4.65 g) as a cloudy oil in 52% yield. 1H NMR (CDCl3, 400 MHz): δ (ppm) 1.45 (t, J=7.1 Hz, 3H), 4.18-4.35 (m, 2H), 7.69 (d, J=579.6 Hz, 1H), 8.10 (s, 1H), 8.23 (s, 1H), 8.27 (s, 1H); 31P NMR (CDCl3, 161.8 MHz): δ (ppm) 19.59 (J=580.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309737B2
Source datasetuspto-grants-2012_11
ORD IDord-d0fae7b1b1564edc84021bd0574b5d64
Source noteuspto-grants-2012_11