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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9939생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/9939

반응식

참여 물질

역할이름HCID투입량
반응물Butyl vinyl etherHCID 8108—
반응물Phosphorus oxychlorideHCID 24813—
반응물N-MethylformanilideHCID 66737—
반응물TriphosgeneHCID 94429—
반응물3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indoleHCID 736229—
용매AcetonitrileHCID 6342—
생성물3-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-YL]-2-propenalHCID 5339529169%

반응 조건

온도5 °C

반응 단계

To a solution of N-methylformanilide (30 g), butyl vinyl ether (22.2 g) in 15 ml of acetonitrile under stirring at 5° C., a solution of bis-trichloromethylcarbonate (26.1 g) in 70 ml of acetonitrile is added dropwise in 80 min. The reaction mixture is kept under stirring at 5° C. overnight, then phosphorus oxychloride (31.4 g) is added dropwise in 30 minutes, then the reaction mixture is stirred at 5° C. for 15 minutes. 3-[3-(4-Fluorophenyl)-1-(1-Methylethyl)-1H-Indole (35.8 g) and acetonitrile (25 ml) are added. The mixture is warmed to 80° C. and kept under stirring for about 24 hours. The reaction mixture is worked up as described in Example 3b to give the product (69% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091382B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-3d53efdb7a5449338c2b2634ab6dd476
출처 메모uspto-grants-2006_08