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HRID 1858874Erstellt: 25. Oktober 2026

3,5-Dimethylaniline → 4-[4'-(4"-Nitrophenylazo)phenylazo]-3,5-dimethylaniline

https://huagongshe.com/reaction/1858874

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-DimethylanilineHCID 7949—
EduktDisperse orange 3HCID 12896—
EduktSodium HydroxideHCID 14798—
EduktSodium AcetateHCID 517045—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt4-[4'-(4"-Nitrophenylazo)phenylazo]-3,5-dimethylanilineHCID 5439382161%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

A 4 g (16.53 mmol) amount of 4-amino-4'-nitroazobenzene (Disperse Orange 3) was dissolved in ice-cooled acetic acid (100 mL) containing 8 mL of 98% sulfuriic acid. Sodium nitrite (1.48 g, 21.40 mmol) dissolved in a small amount of water (less than 2 mL) was added dropwise to the stirred solution. The reaction temperature was maintained at 5° C. After 6 h of stirring, 3,5-dimethylaniline (5.0 g, 41.30 mmol) in 10 mL of acetic acid was added followed by slow addition of sodium acetate (4.10 g, 50.0 mmol). The resulting red solution was stirred at 5° C. for an additional 16 h. A 10% sodium hydroxide solution was slowly added to neutralize the reaction mixture. The precipitates formed were collected by filtration, washed with water several times, dissolved in THF, and dried over magnesium sulfate. Solvent was evaporated, and a dark red powder was obtained by precipitation in n-hexane. The solid was further purified by column chromatography (silica gel; THF: n-hexane=4 6), affording 3.51 g (61%) of 4-[4'-(4"-nitrophenylazo)phenylazo]-3,5-dimethylaniline as a dark red solid product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06153272
Quelldatensatzuspto-grants-2000_11
ORD IDord-f4627ddeb8094052b45573f08384758d
Quellennotizuspto-grants-2000_11