関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1-Acetylpiperidine | HCID 12058 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | Ethyl (3R)-4-cyano-3-hydroxybutanoate | HCID 2733879 | — |
| 溶媒 | Tetrahydrofuran heptane | HCID 21263495 | — |
| 生成物 | (R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrile | HCID 22851143 | — |
反応手順
To a stirred -10° C. solution of 1-acetylpiperidine (127 g, 1.0 mol) in tetrahydrofuran (1.0 L) is slowly added a solution of lithium diisopropylamide in tetrahydrofuran-heptane (0.5 L of 2M) while maintaining the temperature between -40° C. to -50° C., and the mixture is stirred at -20° C. to -30° C. for 30 minutes. (R)-4-cyano-3-hydroxybutyric acid, ethyl ester (Brower, supra) (40 g, 0.25 mol) as a solution in 200 mL of tetrahydrofuran is then added to the previous mixture. The reaction mixture is stirred for 30 minutes at -25° C. to -20° C., and transferred to a 2.2N aqueous hydrochloric acid solution (1 L). The aqueous layer is extracted with 500 mL of ethyl acetate, the aqueous layer is separated and extracted with 100 mL of ethyl acetate, the extracts are combined and concentrated in vacuo to afford (R)-ε-hydroxy-α,γ-dioxo-1-piperidineheptanenitrile as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05298627 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-47b878ee2d1f4cdf92f13e887b431019 |
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| 出典メモ | uspto-grants-1994_03 |
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