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HRID 27165作成日:2026年10月26日

Dimethylformamide → N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamide

https://huagongshe.com/reaction/27165

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Benzyl chloroformateHCID 10387—
反応物Potassium CarbonateHCID 11430—
反応物N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(p-toluidino)acetamideHCID 10042154—
溶媒ChloroformHCID 6212—
生成物N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamideHCID 2046050984.8%

反応手順

A mixture of N-[2(3,4-dimethoxyphenyl)ethyl]2-(p-toluidino)acetamide (3.6 g) and anhydrous potassium carbonate (2.5 g) was added to anhydrous dimethylformamide (25 ml). The mixture was vigorously stirred under ice cooling and to the solution was dropwise added over 20 minutes an anhydrous chloroform solution (5 ml) containing benzyl chloroformate (2.04 g). The reaction mixture was poured into ice-water and extracted with chloroform. The extract was washed with water, dried and the solvent was distilled off. The residue was crystallized by treating with ether to give N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamide (4.3 g), mp 81° to 85° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04220647
出典データセットuspto-grants-1980_09
ORD IDord-5a341a5ba17e4d23a8c6da3051bc6881
出典メモuspto-grants-1980_09