関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-Iodopyridine | HCID 70714 | — |
| 反応物 | rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetate | HCID 10154103 | — |
| 反応物 | HCID 178418546 | HCID 178418546 | — |
| 反応物 | HCID 178418918 | HCID 178418918 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | (1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-ol | HCID 59486121 | 55.3% |
反応手順
To a solution of 3-Iodopyridine (13.0 g, 63.3 mmol) in THF (30 mL) was added i-PrMgCl (38.0 mL, 76.0 mmol) at 3-9° C. After stirring was continued at room temperature for 30 min, CuCN (567 mg, 6.33 mmol) was added to the solution at 2° C. After stirring was continued at 3° C. for 30 min, to the resulting solution were added (1R,4S)-4-hydroxycyclopent-2-enyl acetate (3.00 g, 21.1 mmol) in THF (30 mL). The whole mixture was stirred at the room temperature for 2 h, and diluted with saturated NH4Cl with vigorous stirring. The products were extracted with EtOAc three times, and the combined layers were dried over Na2SO4. After concentration under reduced pressure, the residue was purified by column chromatography (NH, Hexane/EtOAc=4/1) to yield (1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-ol (1.88 g, 55%) as yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08071591B2 |
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| 出典データセット | uspto-grants-2011_12 |
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| ORD ID | ord-d22fd8b1de6d415ca3aaf9eda8aed6b2 |
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| 出典メモ | uspto-grants-2011_12 |
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