HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960187Generated: October 30, 2026
(3-Aminopropyl)triethoxysilane → HCID 178476784, compound
https://huagongshe.com/reaction/1960187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3-Aminopropyl)triethoxysilane | HCID 13521 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | 1-Iodo-3,5-bis(trifluoromethyl)benzene | HCID 630970 | — |
| Reactant | HCID 178527020 | HCID 178527020 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178476784 | HCID 178476784 | 52% |
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 (1M), 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08410313B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-8848741f20cb45138d72b64939ab2cba |
|---|
| Source note | uspto-grants-2013_04 |
|---|