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HRID 2964作成日:2026年10月24日

P-Anisidine → 2-bromo-N-(4-methoxyphenyl)acetamide

https://huagongshe.com/ja/reaction/2964

反応式

関与物質

役割名称HCID仕込み量
反応物P-AnisidineHCID 7732—
反応物Bromoacetyl bromideHCID 61147—
反応物DiisopropylethylamineHCID 81531—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-bromo-N-(4-methoxyphenyl)acetamideHCID 532213—

反応条件

温度-20 °C

反応手順

The title compound was prepared via a modification of the literature procedure (Vloon, W. J.; Kruk, C.; Pandit, U. K.; Hofs, H. P.; McVie, J. G. J. Med Chem. 1987, 30, 20-4.). To a solution of 4-methoxyaniline (4.93 g, 40.0 mmol) in methylene chloride (200 mL) was added diisopropylethylamine (7.66 mL, 44.0 mmol). The resulting mixture was cooled to -20° C., and bromoacetyl bromide (3.82 mL, 44.0 mmol) was added slowly. The reaction mixture was warmed to room temperature over 20 minutes and stirred additional 30 minutes. The reaction mixture was diluted with water (100 mL), stirred for 30 minutes and the organic layer was separated. The organic layer was washed with water (2×100 mL), brine (100 mL), dried over magnesium sulfate and concentrated in vacuo to afford a beige solid (9.68 g) which was recrystallized from ethyl acetate to provide bromo-N-(4'-methoxyphenyl)acetamide as a whim crystal (6.31 g, 65%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731438
出典データセットuspto-grants-1998_03
ORD IDord-a73c3e09e44447508491ea934b7c975c
出典メモuspto-grants-1998_03