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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 371375Erstellt: 25. Oktober 2026

Hydrogen Cyanide → 2-Ethylhex-2-Enal

https://huagongshe.com/reaction/371375

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen CyanideHCID 768—
Edukt2-Ethylhex-2-EnalHCID 12582—
EduktN-methyl-2-pyrrolidoneHCID 13387—
EduktSodium HydroxideHCID 14798—
LösungsmittelEthylene GlycolHCID 174—
Produkt2-Ethylhex-2-EnalHCID 12582—
Produkt3-Formyl-2-propylpentanenitrileHCID 13205740—

Reaktionsbedingungen

Temperatur115 °C

Reaktionsschritte

195 parts of 97% strength 2-ethylhex-2-enal, 77 parts of N-methylpyrrolidone and 33 parts of stabilizer-free hydrocyanic acid were initially taken in a stirred autoclave. The autoclave was closed, 18 parts of a 5% strength solution of sodium hydroxide in ethylene glycol were then metered in over about 5 minutes, and the autoclave was then heated at 115° C. for 40 minutes. After the reaction was complete, the product was removed via a siphon tube, and introduced onto a mixture of 5 parts of 85% strength phosphoric acid and 300 parts of ice. The organic phase was taken up in 300 parts of diethyl ether, and the solution was washed with three times 500 parts of water, dried over magnesium sulfate and fractionally distilled. 55 parts of 2-ethylhex-2-enal and 117 parts of 3-cyano-2-ethylhexanal were obtained in a boiling range of from 35° to 47° C./0.05 mbar. This corresponded to a yield of 68.9% of theory, based on 2-ethylhex-2-enal converted, or 62.6% of theory, based on hydrocyanic acid employed.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04532082
Quelldatensatzuspto-grants-1985_07
ORD IDord-ec4e8cfefdfe4ae0a82d730f3b6f3ab8
Quellennotizuspto-grants-1985_07