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HRID 36431作成日:2026年10月26日

Hydrochloric Acid → N-methyl-2-(2-phenoxyphenyl)-2-oxoacetamide

https://huagongshe.com/reaction/36431

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物DiphosgeneHCID 10426—
反応物Thionyl ChlorideHCID 24386—
反応物N-MethylformamideHCID 31254—
反応物2-Phenoxybenzoic acidHCID 75237—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物N-methyl-2-(2-phenoxyphenyl)-2-oxoacetamideHCID 1178009161%

反応条件

温度10 °C

反応手順

N-Methylformamide (2.36 g, 40.0 mmol) and triethyl amine (8.08 g, 80.0 mmol) were dissolved in toluene (40 ml). Trichloromethylchloroformate (3.96 g, 20.0 mmol) was added dropwise slowly under ice-cooling while maintaining the inner temperature at 10° C. or lower. The mixture was stirred at the same temperature for 1 hour. A large amount of insoluble materials were precipitated. To the mixture was added 2-phenoxybenzoyl chloride which was prepared from 2-phenoxybenzoic acid (4.28 g, 20.0 mmol) and thionyl chloride (2.86 g, 24.0 mmol). The resulting mixture was stirred at bath temperature of 40° to 50° C. for 26 hours. 5N-Hydrochloric acid (12 ml) and acetone (20 ml) were added, and the mixture was stirred for 12 hours. Water was added to the mixture, which was then extracted with toluene and purified by column chromatography on silica gel to obtain the title compound (3.11 g, Yield: 61.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414122
出典データセットuspto-grants-1995_05
ORD IDord-3f1a560936404ceab29a4525d3e42212
出典メモuspto-grants-1995_05