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HRID 342767作成日:2026年10月26日

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

https://huagongshe.com/reaction/342767

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-chloro-4-fluoro-HCID 9604—
反応物Sodium hydrideHCID 24758—
反応物5-(prop-2-en-1-yloxy)-1H-indoleHCID 14239230—
溶媒TetrahydrofuranHCID 8028—
生成物5-allyloxy-N-(4-chlorophenyl)indoleHCID 54410488—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05859051
出典データセットuspto-grants-1999_01
ORD IDord-795c175dcce247b2aacf26afcf06a6ac
出典メモuspto-grants-1999_01