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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18400Erstellt: 24. Oktober 2026

Ethyl Acetate → 3-(t-Butyldiphenylsilyloxy)-3-(4-pyridyl)propylamine

https://huagongshe.com/de/reaction/18400

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium HydroxideHCID 14798—
EduktAluminium lithium hydrideHCID 21226445—
Edukt3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrileHCID 21974219—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-(t-Butyldiphenylsilyloxy)-3-(4-pyridyl)propylamineHCID 12136644—

Reaktionsschritte

Lithium aluminum hydride (299 mg, 7.87 mmol) was suspended in anhydrous diethyl ether (10 ml) under a nitrogen atmosphere, a solution of the obtained 3-(t-butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile (1.00 g, 2.59 mmol) in anhydrous diethyl ether (15 ml) was added dropwise to the suspension under ice-cooling with stirring over eight minutes, and the mixture was stirred at room temperature for 75 minutes. Ethyl acetate (15 ml) was added to the reaction mixture under ice-cooling, water (0.28 ml), a 15% aqueous sodium hydroxide solution (0.28 ml) and water (0.85 ml) were added thereto successively, and the whole was stirred at room temperature for 10 minutes. The reaction mixture was dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the target compound (180.0 mg, yellow oily matter, 17.8%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741346B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e1396d93e9d0446f8ff1ba7a7f83be1d
Quellennotizuspto-grants-2010_06