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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371375Generated: October 25, 2026

Hydrogen Cyanide → 2-Ethylhex-2-Enal

https://huagongshe.com/reaction/371375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen CyanideHCID 768—
Reactant2-Ethylhex-2-EnalHCID 12582—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium HydroxideHCID 14798—
SolventEthylene GlycolHCID 174—
Product2-Ethylhex-2-EnalHCID 12582—
Product3-Formyl-2-propylpentanenitrileHCID 13205740—

Reaction Conditions

Temperature115 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04532082
Source datasetuspto-grants-1985_07
ORD IDord-ec4e8cfefdfe4ae0a82d730f3b6f3ab8
Source noteuspto-grants-1985_07