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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27678Erstellt: 24. Oktober 2026

Formamide → 2-((4-(Diethylamino)phenyl)azo)-5-nitrobenzonitrile

https://huagongshe.com/de/reaction/27678

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormamideHCID 713—
EduktAcetic AnhydrideHCID 7918—
EduktSodium AcetateHCID 517045—
Edukt2-Bromo-4-nitro-4'-(N,N-diethylamino)azobenzeneHCID 23341444—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelButyl AcetateHCID 31272—
Produkt2-((4-(Diethylamino)phenyl)azo)-5-nitrobenzonitrileHCID 301582275%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

2-Bromo-4-nitro-4'-(N,N-diethylamino)azobenzene (1.9 parts), copper (I) iodide (0.95 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 temperatures is maintained at 110° C. for 31/2 hours when reaction is adjudged complete by thin layer chromatography. The solvent is removed at 80° C. under reduced pressure and the residue is slurried in water (250 parts), collected and dried. 2-Cyano-4-nitro-4'-(N,N-diethylamino)azobenzene is obtained in 75% yield and requires no purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04222935
Quelldatensatzuspto-grants-1980_09
ORD IDord-99c02245faa74ee4a81ad4cfc92bd3be
Quellennotizuspto-grants-1980_09