関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetaldehyde | HCID 177 | — |
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Phenyl(piperidin-4-yl)methanone | HCID 226102 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Phenyl-piperidin-4-yl-methanol | HCID 339086 | 85% |
反応手順
4-benzoyl-piperidine (7.35 g, 39.05 mmol) was added over a solution of 25 g of (−)-DIP-Cl (78.125 mmol) in dichloromethane (75 mL, dry) cooled down to 0-2° C. After reacting for 72 h, 5.2 mL of acetaldehyde (92.2 mmol) were added and stirred at room temperature for 3 h. 71 mL of an aqueous NaOH (6N) solution, dichloromethane and saturated aqueous NaCl solution were added. The phases were separated and the usual treatment of the organic phase provided (−)-α-phenyl-4-piperidinemethanol as a white solid with a m.p.=48-50° C. in a 85% yield (86% ee).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06518284B2 |
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| 出典データセット | uspto-grants-2003_02 |
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| ORD ID | ord-b8dcaf8978c0403693775825924e6924 |
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| 出典メモ | uspto-grants-2003_02 |
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