참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 1-Acetylpiperidine | HCID 12058 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | Ethyl (3R)-4-cyano-3-hydroxybutanoate | HCID 2733879 | — |
| 용매 | Tetrahydrofuran heptane | HCID 21263495 | — |
| 생성물 | (R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrile | HCID 22851143 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05298627 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-47b878ee2d1f4cdf92f13e887b431019 |
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| 출처 메모 | uspto-grants-1994_03 |
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