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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
Edukt1-AcetylpiperidineHCID 12058—
EduktLithium diisopropylamideHCID 2724682—
EduktEthyl (3R)-4-cyano-3-hydroxybutanoateHCID 2733879—
LösungsmittelTetrahydrofuran heptaneHCID 21263495—
Produkt(R)-epsilon-hydroxy-alpha,gamma-dioxo-1-piperidineheptanenitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05298627
Quelldatensatzuspto-grants-1994_03
ORD IDord-47b878ee2d1f4cdf92f13e887b431019
Quellennotizuspto-grants-1994_03