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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171633생성일: 2026년 10월 26일

Benzaldehyde → (E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-one

https://huagongshe.com/reaction/1171633

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물PyrrolidineHCID 31268—
반응물1-Tritylpiperidin-4-oneHCID 2748414—
용매BenzeneHCID 241—
용매Ethyl AcetateHCID 8857—
생성물(E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-oneHCID 6876571274%

반응 단계

To a solution of 1-(triphenylmethyl)piperidin-4-one (4.22 g) in benzene (50 ml) was added pyrrolidine (1.02 ml) at room temperature, and the resulting mixture was refluxed for 3 hours. After cooling to room temperature, benzaldehyde (1.26 ml) was added to the reaction mixture, and the resulting mixture was furthermore refluxed for 2 hours. After refluxing, the reaction mixture was diluted with ethyl acetate, 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 (1:3) as the eluent to afford the title compound (3.92 g, yield: 74%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829580B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-2834e8323229450fa7d7f6c49b06546f
출처 메모uspto-grants-2010_11