Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzaldehyde → (E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzaldehyde | HCID 240 | — |
| 반응물 | Pyrrolidine | HCID 31268 | — |
| 반응물 | 1-Tritylpiperidin-4-one | HCID 2748414 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-one | HCID 68765712 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07829580B2 |
| 출처 데이터셋 | uspto-grants-2010_11 |
| ORD ID | ord-2834e8323229450fa7d7f6c49b06546f |
| 출처 메모 | uspto-grants-2010_11 |