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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1701271Erstellt: 24. Oktober 2026

Nitrone → 4-(2'-cyano-4'-bromo-6'-methylphenylazo)-N,N-diethylaniline

https://huagongshe.com/de/reaction/1701271

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitroneHCID 6350—
EduktNitrobenzeneHCID 7416—
Edukt2,6-LutidineHCID 7937—
Edukt4-[(2,4-dibromo-6-methylphenyl)diazenyl]-N,N-diethylanilineHCID 12525527—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Produkt4-(2'-cyano-4'-bromo-6'-methylphenylazo)-N,N-diethylanilineHCID 2034745515,1%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A stirred mixture of 4-(2',4'-dibromo-6'-methylphenylazo)-N,N-diethylaniline (4.25 parts), copper (I) iodide (2.0 parts), formaldoxime trimer (1.75 parts), 2,6-lutidine (2.15 parts), and nitrobenzene (150 parts) was heated to 95° C. for 6 hours when thin layer chromatography showed reaction to be complete. The mixture was cooled, filtered and the nitrobenzene was removed by steam distillation. Crystallisation of the solid product from ethanol gave 4-(2'-cyano-4'-bromo-6'-methylphenylazo)-N,N-diethylaniline (Found: C, 58.2; H, 5.4; Br, 21.7; N, 15.2. C18H19BrN4 requires C, 58.2; H, 5.15; Br, 21.55; N, 15.1%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04192800
Quelldatensatzuspto-grants-1980_03
ORD IDord-54d85bb108784b8bbeaa97feaa27ce35
Quellennotizuspto-grants-1980_03