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HRID 2304919作成日:2026年10月25日

Ethanol → N-methyl-2-phenoxybenzamide

https://huagongshe.com/reaction/2304919

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物MethylamineHCID 6329—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2-Phenoxybenzoic acidHCID 75237—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物N-methyl-2-phenoxybenzamideHCID 325579183.5%

反応条件

温度0 °C

反応手順

At 0° C., 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (22.4 g, 0.117 mol) was added to a solution of 2-phenoxybenzoic acid (25.0 g, 0.117 mol) and 1-hydroxybenzotrizole (15.8 g, 0.117 mmol) in DCM (80 ml) and N,N-dimethylformamide (160 ml). The reaction mixture was stirred for 20 min at 0° C. A 8.0 M solution of methylamine in ethanol (290 ml, 2.33 mol) was added. The reaction mixture was stirred for 16 hours at room temperature. It was diluted with ethyl acetate (200 ml) and washed with a 10% aqueous solution of sodium hydrogen sulphate (300 ml). The aqueous phase was extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (300 g), using ethyl acetate/heptane 1:1 as eluent, to give 22.2 g of N-methyl-2-phenoxybenzamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06437147B1
出典データセットuspto-grants-2002_08
ORD IDord-61ceb5b90bd140afa4629d6537410d1f
出典メモuspto-grants-2002_08