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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18400생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium HydroxideHCID 14798—
반응물Aluminium lithium hydrideHCID 21226445—
반응물3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrileHCID 21974219—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물3-(t-Butyldiphenylsilyloxy)-3-(4-pyridyl)propylamineHCID 12136644—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741346B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e1396d93e9d0446f8ff1ba7a7f83be1d
출처 메모uspto-grants-2010_06