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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9936생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/9936

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcroleinHCID 7847—
반응물3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indoleHCID 736229—
용매AcetonitrileHCID 6342—
생성물3-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-YL]-2-propenalHCID 53395291—

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091382B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b3433aa238654c3094a8e2f17d344453
출처 메모uspto-grants-2006_08