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HRID 654464作成日:2026年10月25日

3-Cyclohexene-1-carboxaldehyde → Z-2-(4-fluorophenyl)-3-(3-cyclohexenyl)-propenal

https://huagongshe.com/reaction/654464

反応式

関与物質

役割名称HCID仕込み量
反応物3-Cyclohexene-1-carboxaldehydeHCID 7508—
反応物Sodium HydroxideHCID 14798—
反応物2-(4-fluorophenyl)acetaldehydeHCID 11126322—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物Z-2-(4-fluorophenyl)-3-(3-cyclohexenyl)-propenalHCID 2161583441%

反応条件

温度10 °C

反応手順

5.5 g of sodium hydroxide in 30 ml of water are added to a solution of 40 g of 3-cyclohexenecarbaldehyde in 300 ml of methanol. The reaction mixture is cooled to 10° C., and 49.7 g of 4-fluorophenylacetaldehyde are rapidly added dropwise, the temperature of the solution not exceeding 30° C. After the mixture has been stirred for 2 hours at room temperature, 200 ml of water are added to the colorless reaction solution and the resulting emulsion is extracted by shaking with methyl tert-butyl ether. The organic phase is separated off, and 34 g (41%) of Z-2-(4-fluorophenyl)-3-(3-cyclohexenyl)-propenal are obtained under 0.5 mbar and at 136°-142° C. by distillation of the remaining residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05132318
出典データセットuspto-grants-1992_07
ORD IDord-3d8f3edfab3d4102a408ac7aad6c81e4
出典メモuspto-grants-1992_07