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HRID 2456作成日:2026年10月24日

2-Methoxyaniline → 4-Chloromethyl-N-(2-methoxyphenyl)-N-(1,3-dioxolan-2-yl)methylbenzamide

https://huagongshe.com/ja/reaction/2456

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethoxyanilineHCID 7000—
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物4-(Chloromethyl)benzoyl chlorideHCID 70136—
反応物1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
溶媒DichloromethaneHCID 6344—
生成物4-Chloromethyl-N-(2-methoxyphenyl)-N-(1,3-dioxolan-2-yl)methylbenzamideHCID 1969000647.9%

反応条件

温度80 °C

反応手順

In an atmosphere of argon, a mixture consisting of o-anisidine (500 mg, 4.06 mmol), triethylamine (1.6 ml, 11.5 mmol) and 2-bromomethyl-1,3-dioxolan (0.96 ml, 8.18 mmol) was stirred at 80° C. for 4 days, dissolved in methylene chloride (8 ml) and then, with cooling in an ice bath, mixed with 20% sodium hydroxide aqueous solution (4 ml) and 4-chloromethylbenzoyl chloride (768 mg, 4.06 mmol). After 1 hour of stirring at the same temperature, the resulting mixture was extracted with methylene chloride, washed with 10% citric acid aqueous solution and saturated brine and then dried on anhydrous sodium sulfate. Thereafter, the solvent was removed by evaporation, and the resulting residue was purified by subjecting it to a silica gel column chromatography (ethyl acetate:hexane=2:5) to obtain 704 mg (47.9%) of the title compound in the form of colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728835
出典データセットuspto-grants-1998_03
ORD IDord-15921a54043f4c95b9921819784b62d3
出典メモuspto-grants-1998_03