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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371375생성일: 2026년 10월 26일

Hydrogen Cyanide → 2-Ethylhex-2-Enal

https://huagongshe.com/reaction/371375

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen CyanideHCID 768—
반응물2-Ethylhex-2-EnalHCID 12582—
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물Sodium HydroxideHCID 14798—
용매Ethylene GlycolHCID 174—
생성물2-Ethylhex-2-EnalHCID 12582—
생성물3-Formyl-2-propylpentanenitrileHCID 13205740—

반응 조건

온도115 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04532082
출처 데이터셋uspto-grants-1985_07
ORD IDord-ec4e8cfefdfe4ae0a82d730f3b6f3ab8
출처 메모uspto-grants-1985_07