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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1050494Erstellt: 26. Oktober 2026

Sulfuric Acid → 4-((2,4-Dinitrophenyl)diazenyl)-2,5-bis(2-ethylhexyloxy)aniline

https://huagongshe.com/reaction/1050494

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
Edukt2,4-DinitroanilineHCID 7321—
EduktNitrosylsulfuric acidHCID 82157—
Edukt2,5-Bis(2-ethylhexyloxy)anilineHCID 89601757—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelPropionic AcidHCID 1032—
LösungsmittelSulfamic AcidHCID 5987—
Produkt4-((2,4-Dinitrophenyl)diazenyl)-2,5-bis(2-ethylhexyloxy)anilineHCID 8960207439%

Reaktionsbedingungen

Temperatur3 °C

Reaktionsschritte

2,4-Dinitroaniline (3.7 g, 0.02 mol) is suspended in a mixture of acetic acid (20 ml) and propionic acid (10 ml) and cooled to 3° C. 40% (w/w) nitrosyl sulfuric acid in sulfuric acid (6.4 g, 0.02 mol) is added dropwise and stirring continued for 30 minutes to give a pale yellow solution. Crude 2,5-bis(2-ethylhexyloxy)aniline (0.02 mol) solution is diluted with IMS (200 ml) and 10% sulfamic acid solution (20 ml) added, followed by ice (200 g). The above pale yellow diazonium salt solution is slowly added with stirring and a dark oil rapidly separated. The mixture is stirred overnight and the water is decanted off. The crude product (8.3 g) is dissolved in 25/75 dichloromethane/hexane and purified over silica gel, the required product eluting with 50/50 hexane/dichloromethane. Evaporation and trituration with methanol gave 4-((2,4-dinitrophenyl)diazenyl)-2,5-bis(2-ethylhexyloxy)-aniline as a violet-blue crystalline solid (4.2 g, 39%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09383621B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-ad3dc1c3e5ec46369746086868cd0366
Quellennotizuspto-grants-2016_07