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HRID 1948683作成日:2026年10月27日

Potassium Carbonate → 6-bromo-1-(4-ethoxyphenyl)-1H-indole

https://huagongshe.com/reaction/1948683

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物L-ProlineHCID 145742—
反応物1-Ethoxy-4-iodobenzeneHCID 220700—
反応物6-BromoindoleHCID 676493—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物6-bromo-1-(4-ethoxyphenyl)-1H-indoleHCID 6692024556.4%

反応手順

A solution of 1.0 g (5 mmol) of 6-bromo-1H-indole, 1.06 g (4.15 mmol) of 4-iodophenetole, 1.45 g of potassium carbonate, 38.1 mg of copper(I) iodide and 42 mg of L-proline in 15 ml of dimethyl sulfoxide is heated at 120° C. for 15 hours. The reaction mixture is then cooled to room temperature, 30 ml of water are added, and the mixture is extracted three times with 20 ml of ethyl acetate each time. After the combined organic phases have been dried over sodium sulfate, the solvent is stripped off in a rotary evaporator, and the crude product is purified by column chromatography on silica gel (n-heptane/ethyl acetate 98:2), giving 0.74 g of 6-bromo-1-(4-ethoxyphenyl)-1H-indole as brownish resin; LC/MS: 317 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08399509B2
出典データセットuspto-grants-2013_03
ORD IDord-d186617ecc044e7e8fe8929a61fdfec6
出典メモuspto-grants-2013_03