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HRID 1884263作成日:2026年10月26日

Tetrahydrofuran → N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamide

https://huagongshe.com/reaction/1884263

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物TriethylamineHCID 8471—
反応物2-(4-Methylphenyl)acetyl chlorideHCID 2760634—
反応物3-Methoxy-4-phenylmethoxyphenylisopropylamineHCID 14579452—
溶媒WaterHCID 962—
生成物N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl)acetamideHCID 2350901470.1%

反応条件

温度0 °C

反応手順

2.30 g (8.48 mmol) of crude 2-(4-benzyloxy-3-methoxyphenyl)-1-methylethylamine, 1.03 g (10.2 mmol) of triethylamine and 25 ml of tetrahydrofuran were mixed and cooled to about 0° C. and then 1.42 g (8.48 mmol) of (4-methylphenyl)acetyl chloride was added dropwise thereto. The mixture was stirred at 0° C. for 30 minutes and further at room temperature for 2 hours. Water was added to the reaction mixture, which was followed by extracted with ethyl acetate, washed with 5% hydrochloric acid and saturated brine subsequently, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was washed with hexane and dried to give 2.40 g of N-[2-(4-benzyloxy-3-methoxyphenyl)-1-methylethyl]-2-(4-methylphenyl) acetamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06762321B2
出典データセットuspto-grants-2004_07
ORD IDord-2db66898ab8045e3b068d5d260c468c6
出典メモuspto-grants-2004_07