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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171634생성일: 2026년 10월 25일

Ethanol → (E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-ol

https://huagongshe.com/reaction/1171634

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Ammonium ChlorideHCID 25517—
반응물Sodium borohydrideHCID 4311764—
반응물(E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-oneHCID 68765712—
용매DichloromethaneHCID 6344—
생성물(E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-olHCID 6876490866.4%

반응 단계

To a solution of (E)-3-benzylidene-1-(triphenylmethyl)piperidin-4-one (3.91 g) in a mixed solvent of ethanol (30 ml) and dichloromethane (30 ml) was added sodium borohydride (0.34 g) under ice-cooling, and the resulting mixture was stirred at room temperature for 2 hours. After stirring, saturated aqueous ammonium chloride solution was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (3:7) as the eluent to afford the title compound (2.61 g, yield: 66%) as a colourless amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829580B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-aaabdc0934d84cf69f0ef928171fa98b
출처 메모uspto-grants-2010_11