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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1972327Erstellt: 25. Oktober 2026

Ethyl Acetate → (2S,3S)-3-(dibenzylamino)-2-hydroxyhexanenitrile

https://huagongshe.com/reaction/1972327

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium CyanideHCID 8929—
EduktSodium BisulfiteHCID 23665763—
Edukt(S)-2-(dibenzylamino)pentanalHCID 44223341—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkt(2S,3S)-3-(dibenzylamino)-2-hydroxyhexanenitrileHCID 4422334268,6%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

To a solution of (S)-2-(dibenzylamino)pentanal (125 g; 0.444 mol) in methanol (375 mL) at 0-5° C. was added a previously cooled (0-5° C.) aqueous solution of sodium bisulfite (69.39 g, 0.667 mol; 150 mole %) in water (530 mL). The reaction mixture was stirred at 0-5° C. for 14 hours. A solution of sodium cyanide (32.02 g; 0.667 mol; 150 mol %) in water (402 mL), followed by ethyl acetate (1.25 L) was added to the above reaction mixture at 0° C. Stirring was continued at ambient temperature for 5 hours, monitoring progress of the reaction by TLC analysis (ethyl acetate/hexane, 1:9). Once the reaction was complete, the ethyl acetate layer was separated, washed with water (2×750 mL) and dried over sodium sulfate. The organic extract was concentrated under reduced pressure, washed with hexanes (200 mL), to provide 94 g of crude product as an off-white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08431733B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-3dc89adeaadc425eafffe0285d377cb8
Quellennotizuspto-grants-2013_04