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HRID 9936作成日:2026年10月25日

Water → 3-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-YL]-2-propenal

https://huagongshe.com/reaction/9936

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物AcroleinHCID 7847—
反応物3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indoleHCID 736229—
溶媒AcetonitrileHCID 6342—
生成物3-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-YL]-2-propenalHCID 53395291—

反応条件

温度60 °C

反応手順

Use of the crude acrolein coming from Example 3a. To a suspension of 3-[3-(4-Fluorophenyl)-1-(1-Methylethyl)-1H-Indole (35.8 g) phosphorus oxychloride (31.4 g) in acetonitrile (35 ml) cooled at 5° C. a solution of crude acrolein (32.3 g from Example 3a) in acetonitrile (40 ml) is added dropwise in 30 minutes. The reaction mixture is then warmed to 60° C. and kept under stirring at 60° C. for 4 hours; water (300 ml) is added and after 1 hour at 60° C. the formed solid is filtered on Buchner and washed with 75 ml of water. The wet solid (49.7 g) is dissolved in toluene (250 ml), celite (1 g) and charcoal (0.5 g) are added and the mixture is stirred at room temperature for 30 minutes. After filtration of the solid, the solvent is distilled off at reduced pressure and the residue is dissolved at 75° C. with isopropanol (72 ml). The solution is cooled at 20° C. and stirred at room temperature for 1 hour. The precipitate is filtered on Buchner, washed twice with isopropanol (15 ml) and dried at 60° C. under vacuum. 30.2 g (70% molar yield) of the product are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091382B2
出典データセットuspto-grants-2006_08
ORD IDord-b3433aa238654c3094a8e2f17d344453
出典メモuspto-grants-2006_08