HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 488111Erstellt: 24. Oktober 2026
Hydrochloric Acid → (R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrile
https://huagongshe.com/de/reaction/488111
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 1-Acetylpiperidine | HCID 12058 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | Ethyl (3R)-4-cyano-3-hydroxybutanoate | HCID 2733879 | — |
| Lösungsmittel | Tetrahydrofuran heptane | HCID 21263495 | — |
| Produkt | (R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrile | HCID 22851143 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05298627 |
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| Quelldatensatz | uspto-grants-1994_03 |
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| ORD ID | ord-47b878ee2d1f4cdf92f13e887b431019 |
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| Quellennotiz | uspto-grants-1994_03 |
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