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HRID 51467作成日:2026年10月25日

Ethyl bromoacetate → Ethyl 4-Methoxyindole-3-acetate

https://huagongshe.com/reaction/51467

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物4-Methoxy-1H-indoleHCID 138363—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 4-Methoxyindole-3-acetateHCID 91078263—

反応手順

To a solution of 2.94 gm (20 mmol) of 4-methoxyindole in 150 ml of tetrahydrofuran was added slowly 13 ml of n-butyl lithium (1.6M in hexane; 20 mmol) followed by the slow addition of 20 ml of zinc chloride (1.0M in ethyl ether; 20 mmol) at 0-5° C. The cooling bath was removed and the solution stirred for 2 hours and then treated with 2.1 ml (25 mmol) of ethyl bromoacetate for 19 hours, diluted with ethyl acetate, washed with water, washed with brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a gradient hexane/10-50% ethyl ether to give starting material (40%) and then product, 2.3 gm, 50%, as an oil. 1H NMR (CDCl3) δ: 1.25 (t, 3H), 3.85 (s, 3H), 3.90 (s, 2H), 4.10 (q, 2H), 6.45 (d, 1H), 6.90 (d, 1H), 6.95 (s, 1H), 7.05 (t, 1H), 8.00 (br s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713645B1
出典データセットuspto-grants-2004_03
ORD IDord-c1d2dc2209614685a7c4ac39f3fb5372
出典メモuspto-grants-2004_03