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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 342767생성일: 2026년 10월 25일

Benzene, 1-chloro-4-fluoro- → 5-allyloxy-N-(4-chlorophenyl)indole

https://huagongshe.com/reaction/342767

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 1-chloro-4-fluoro-HCID 9604—
반응물Sodium hydrideHCID 24758—
반응물5-(prop-2-en-1-yloxy)-1H-indoleHCID 14239230—
용매TetrahydrofuranHCID 8028—
생성물5-allyloxy-N-(4-chlorophenyl)indoleHCID 54410488—

반응 단계

To a solution of sodium hydride (60%, 254 mg, 6.35 mmol) in 15 mL tetrahydrofuran (THF) was added 5-allyloxyindole (Step A; 1.0 g, 5.77 mmol) in 5 mL THF and the mixture was stirred for 1 hour at ambient temperature. 4-fluorochlorobenzene (0.69 mL, 6.35 mmol) was added and the reaction heated to reflux for 21 hours. After cooling, the reaction was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and the crude residue purified by flash chromatography on silica gel (15% ethyl acetate/hexane) to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05859051
출처 데이터셋uspto-grants-1999_01
ORD IDord-795c175dcce247b2aacf26afcf06a6ac
출처 메모uspto-grants-1999_01