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HRID 18400作成日:2026年10月26日

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

https://huagongshe.com/reaction/18400

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium HydroxideHCID 14798—
反応物Aluminium lithium hydrideHCID 21226445—
反応物3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrileHCID 21974219—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物3-(t-Butyldiphenylsilyloxy)-3-(4-pyridyl)propylamineHCID 12136644—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741346B2
出典データセットuspto-grants-2010_06
ORD IDord-e1396d93e9d0446f8ff1ba7a7f83be1d
出典メモuspto-grants-2010_06