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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2210621Erstellt: 23. Oktober 2026

Ethylenediamine → 2-Amino-1,5-naphthalenedisulfonic acid

https://huagongshe.com/de/reaction/2210621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylenediamineHCID 3301—
Edukt2-Amino-5-hydroxynaphthalene-1,7-disulphonic acidHCID 81024—
Edukt4,5,6-Trifluoro-1,2,3-triazineHCID 13899144—
EduktDifluorotriazineHCID 19878636—
Produkt2-Amino-1,5-naphthalenedisulfonic acidHCID 8338100%

Reaktionsschritte

31.9 g of 2-amino-5-hydroxy-naphthalene-1,7-disulphonic acid are subjected to a condensation reaction with trifluorotriazine as described in Example 1. 5.0 g of ethylenediamine are added to the solution of the resulting difluorotriazine compound at 0°, a pH of 5.5-6.5 being maintained. The condensation has ended after 2 to 3 hours. A diazo compound obtained by the customary route by diazotisation of 30.3 g of 2-amino-naphthalene-1,5-disulphonic acid is added to the reaction product of the formula ##STR20## which is largely present as a suspension, the pH simultaneously being kept at pH 7.0-7.5 by sprinkling in sodium bicarbonate. When the coupling has ended, the dyestuff of the formula ##STR21## which has precipitated as a sparingly soluble product, is filtered off with suction and stirred in 1 l of water again. 16.9 g of 2,4,6-trifluoro-5-chloro-pyrimidine are added dropwise at 0°-5°, during which a pH of 7.5-8.0 is maintained with dilute sodium hydroxide solution. The dyestuff dissolves during the condensation reaction. When the condensation has ended (thin layer chromatogram), the dyestuff is salted out, filtered off with suction, dried and ground. The red powder dissolves readily in water and dyes cotton a clear scarlet (colour code number 6).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05459246
Quelldatensatzuspto-grants-1995_10
ORD IDord-a2862839424f4443997a4deed569a808
Quellennotizuspto-grants-1995_10