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HRID 1618067作成日:2026年10月25日

(3-Aminopropyl)triethoxysilane → HCID 178476782、化合物

https://huagongshe.com/reaction/1618067

反応式

関与物質

役割名称HCID仕込み量
反応物(3-Aminopropyl)triethoxysilaneHCID 13521—
反応物Benzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物HCID 178527020HCID 178527020—
触媒palladium(II) acetateHCID 167845—
溶媒Hydrochloric AcidHCID 313—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178476782HCID 17847678228%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08765966B2
出典データセットuspto-grants-2014_07
ORD IDord-16853e06397e4cd0a30473d62101fef7
出典メモuspto-grants-2014_07