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HRID 27168作成日:2026年10月25日

2-((4-Chlorophenyl)amino)acetic acid → N-[2-(3,4-dibenzyloxyphenyl)ethyl]-2-(p-chloroanilino)acetamide

https://huagongshe.com/reaction/27168

反応式

関与物質

役割名称HCID仕込み量
反応物2-((4-Chlorophenyl)amino)acetic acidHCID 230717—
反応物3,4-Bis(benzyloxy)phenethylamine hydrochlorideHCID 423869—
溶媒BenzeneHCID 241—
生成物N-[2-(3,4-dibenzyloxyphenyl)ethyl]-2-(p-chloroanilino)acetamideHCID 2046056750.4%

反応条件

温度190 °C

反応手順

A mixture of 3,4-dibenzyloxyphenethylamine (36.2 g) and p-chloroanilinoacetic acid (20 g) was stirred for 3 hours at 190° C. The reaction mixture was dissolved in benzene. The solution was washed with a diluted potassium carbonate aqueous solution and dried. The solvent was distilled off from the benzene solution and the residue obtained was purified by column chromatography on silica gel to give N-[2-(3,4-dibenzyloxyphenyl)ethyl]-2-(p-chloroanilino)acetamide (27.2 g), mp 121° 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-d32a625541c54a508541c94c4e741306
出典メモuspto-grants-1980_09