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HRID 371375作成日:2026年10月26日

Hydrogen Cyanide → 2-Ethylhex-2-Enal

https://huagongshe.com/reaction/371375

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen CyanideHCID 768—
反応物2-Ethylhex-2-EnalHCID 12582—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物Sodium HydroxideHCID 14798—
溶媒Ethylene GlycolHCID 174—
生成物2-Ethylhex-2-EnalHCID 12582—
生成物3-Formyl-2-propylpentanenitrileHCID 13205740—

反応条件

温度115 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04532082
出典データセットuspto-grants-1985_07
ORD IDord-ec4e8cfefdfe4ae0a82d730f3b6f3ab8
出典メモuspto-grants-1985_07