참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | (E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-one | HCID 68765712 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-ol | HCID 68764908 | 66.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07829580B2 |
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| 출처 데이터셋 | uspto-grants-2010_11 |
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| ORD ID | ord-aaabdc0934d84cf69f0ef928171fa98b |
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| 출처 메모 | uspto-grants-2010_11 |
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