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HRID 27681作成日:2026年10月26日

Formamide → Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-

https://huagongshe.com/reaction/27681

反応式

関与物質

役割名称HCID仕込み量
反応物FormamideHCID 713—
反応物Acetic AnhydrideHCID 7918—
反応物Acetamide, N-[2-[2-(2-bromo-4,6-dinitrophenyl)diazenyl]-5-(diethylamino)phenyl]-HCID 104287—
反応物Sodium AcetateHCID 517045—
触媒Cupric ChlorideHCID 24014—
溶媒Butyl AcetateHCID 31272—
生成物Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-HCID 9038396%

反応条件

温度110 °C

反応手順

2-Bromo-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene (2.4 parts), copper (II) chloride (0.67 parts), anhydrous sodium acetate (1.2 parts), formamide (1.8 parts), acetic anhydride (2.0 parts) and n-butyl acetate (44 parts) are mixed together and heated, with stirring, to 110° C. during 15 minutes. The temperature is maintained for 5 hours after which time the reaction is complete. The mixture is cooled to room temperature and poured into petroleum-ether (boiling range 60-80°) (400 parts). The precipitate is collected, washed with petroleum-ether (100 parts) and dried. 2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene is obtained in 96% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04222935
出典データセットuspto-grants-1980_09
ORD IDord-a9221bcf0bbb4c9692966241d39232ec
出典メモuspto-grants-1980_09