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HRID 27679Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/27679

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormamideHCID 713—
EduktPropionic anhydrideHCID 31263—
EduktAcetamide, N-[2-[2-(2-bromo-4,6-dinitrophenyl)diazenyl]-5-(diethylamino)phenyl]-HCID 104287—
EduktSodium AcetateHCID 517045—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelButyl AcetateHCID 31272—
ProduktAcetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-HCID 9038383,5%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

2-Bromo-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene (2.4 parts), copper (I) iodide (0.95 parts), anhydrous sodium acetate (1.2 parts), formamide (1.8 parts), propionic anhydride (2.6 parts) and n-butyl acetate (44 parts) are mixed together are heated, with stirring, to 110° C. during 15 minutes. The temperature is maintained for 30 minutes when reaction is adjudged complete by thin layer chromatography. The mixture is cooled to room temperature and poured into petroleum ether (boiling range 60-80° C.) (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 83.5% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04222935
Quelldatensatzuspto-grants-1980_09
ORD IDord-bd6608fb4bfe4cc9af4f818a4bca50c8
Quellennotizuspto-grants-1980_09