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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 576533생성일: 2026년 10월 25일

1-Phenyl-2-propen-1-one → 1,3-Dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one

https://huagongshe.com/reaction/576533

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenyl-2-propen-1-oneHCID 13028—
반응물Potassium HydroxideHCID 14797—
반응물1,4-DioxaneHCID 31275—
반응물1,3-Dimethyl-4-piperidoneHCID 107311—
용매WaterHCID 962—
생성물1,3-Dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-oneHCID 6735711010.8%

반응 조건

온도25 °C

반응 단계

To a stirred solution of 1,3-dimethyl-piperidin-4-one (0.1 g, 0.787 mmol) in mixture of 1,4 dioxane (2 mL) and water (0.1 mL) was added crushed KOH (44 mg, 0.787 mmol). The reaction mixture was stirred at 25° C. for 10 min. To this was added 1-phenylprop-2-en-1-one (103 mg, 0.787 mmol) dropwise. The reaction mixture was stirred at 25° C. for 2 h. The reaction mixture was concentrated under reduced pressure and the residue was diluted with water (10 mL) and EtOAc (20 mL), the organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting crude product was purified by column chromatography on neutral alumina (eluted with EtOAc:Hexanes, 1:99) to afford 1,3-dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one as an oil (22 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040519B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-0c551d20fef6440ca1f200327530665c
출처 메모uspto-grants-2015_05