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Benzene, 1-chloro-4-fluoro- → 5-allyloxy-N-(4-chlorophenyl)indole
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 hydride | HCID 24758 | — |
| 反応物 | 5-(prop-2-en-1-yloxy)-1H-indole | HCID 14239230 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-allyloxy-N-(4-chlorophenyl)indole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05859051 |
| 出典データセット | uspto-grants-1999_01 |
| ORD ID | ord-795c175dcce247b2aacf26afcf06a6ac |
| 出典メモ | uspto-grants-1999_01 |