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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2210623Erstellt: 27. Oktober 2026

3-Aminobenzenesulfonic acid → 2-Amino-1,5-naphthalenedisulfonic acid

https://huagongshe.com/reaction/2210623

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Aminobenzenesulfonic acidHCID 8474—
EduktSodium CarbonateHCID 10340—
Edukt2-Amino-5-hydroxynaphthalene-1,7-disulphonic acidHCID 81024—
Edukt4,5,6-Trifluoro-1,2,3-triazineHCID 13899144—
LösungsmittelWaterHCID 962—
Produkt2-Amino-1,5-naphthalenedisulfonic acidHCID 8338100%

Reaktionsschritte

31.9 g of 2-amino-5-hydroxynaphthalene-1,7-disulphonic acid are dissolved in 400 ml of water under neutral conditions. 300 g of ice are then added, and 8.8 ml of trifluorotriazine are run in while maintaining a pH of 4.0 to 4.5 with 15% strength sodium carbonate solution. Stirring is continued for 5 minutes, and a neutral solution of 17.3 g of m-sulphanilic acid is then added while maintaining a pH of 5.0 to 5.5 with 15% strength sodium carbonate solution. During acylation, the temperature is allowed to rise to 15° to 20°. A diazo compound obtained in the usual manner by diazotisation of 30.3 g of 2-aminonaphthalene-1,5-disulphonic acid is added to the resulting solution of the reaction product of the formula ##STR15## at 5° to 10°, while simultaneously maintaining the pH at 7.0 to 7.5 by sprinkling in sodium bicarbonate. After coupling is complete, the dyestuff of the formula ##STR16## is salted out, filtered off with suction, dried and milled.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05459245
Quelldatensatzuspto-grants-1995_10
ORD IDord-99e5f17fa37448a69ea6137be3748fa9
Quellennotizuspto-grants-1995_10