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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11460생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/11460

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 1213664417.8%

반응 단계

Lithium aluminum hydride (299 mg, 7.87 mmol) was suspended in anhydrous diethyl ether (10 ml) under a nitrogen atmosphere, and 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. The temperature was raised to room temperature, and the mixture was stirred for 75 minutes. The reaction mixture was cooled with ice, ethyl acetate (15 ml) was added to the reaction mixture, and water (0.28 ml), a 15% aqueous sodium hydroxide solution (0.28 ml) and water (0.85 ml) were added thereto successively. The temperature was raised to room temperature, and the whole was stirred 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 titled compound (180.0 mg, yellow oily matter, 17.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098226B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f849e22082904606b4e01986dc77a519
출처 메모uspto-grants-2006_08