関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | 1,4-Difluorobenzene | HCID 10892 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Phenyl-piperidin-4-yl-methanol | HCID 339086 | — |
| 反応物 | Potassium Benzoate | HCID 23661960 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (+)-4-[(4-Fluorophenoxy)phenyl]methyl-piperidine | HCID 18669358 | 64% |
反応手順
The alcohol prepared above (1.3 g, 4.5 mmol) dissolved in DMSO (10 mL) was added over an NaH (60%, 210 g) suspension in DMSO (5 mL). Potassium benzoate (715 g, 4.5 mmol) and 1,4-difluorobenzene (0.75 mL, 6.86 mmol) were added and the mixture heated (70-75° C.) until the starting substance disappeared. The reaction mixture was poured into water and saturated aqueous NaCl solution, and extracted with ether. The oil obtained was refluxed with a mixture of methanol (17 mL) and an aqueous hydrochloric acid (17 mL) solution for 1 h. The usual working of the reaction provided (−)-4-[(4-fluorophenoxy)phenyl]methyl-piperidine as an oil in a 64% yield. Treatment of this oil with L-dibenzoyltartaric acid in ethanol (96%, 35 mL) provided a precipitate which was filtered (m.p.=193-194° C.). The aminoether was released yielding a white solid with a 98% ee, m.p.=100-102° C., and [α]546−14, c=0.2, CHCl3).
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-bf4a815c6602482ab51787f9371fd8ff |
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| 出典メモ | uspto-grants-2003_02 |
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