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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269374Erstellt: 24. Oktober 2026

Hydrogen Bromide → 1-Bromo-8-hydroxynaphthalene-3,6-disulfonic acid

https://huagongshe.com/de/reaction/269374

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktSodium ChlorideHCID 5234—
EduktH acidHCID 7009—
EduktSodium NitriteHCID 23668193—
Katalysatorcopper(I) bromideHCID 24593—
LösungsmittelWaterHCID 962—
Produkt1-Bromo-8-hydroxynaphthalene-3,6-disulfonic acidHCID 8551989074%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

1-Amino-8-hydroxynaphthalene-3,6-disulfonic acid (72% strength, 44.4 g, 0.1 mol) was stirred in a mixture of water (340 mls) and 48% hydrobromic acid (20 mls). The suspension was cooled to 0-5° C. and sodium nitrite (7.6 g, 0.11 mol) was added in small portions. The mixture was stirred for 2 hours at 0-5° C. and then the excess nitrous acid was destroyed by the addition of sulfamic acid solution. Further 48% hydrobromic acid (70 mls) was added and the mixture cooled to 5° C. A solution of copper (I) bromide (14.4 g, 0.1 mol) in 48% hydrobromic acid (30 mls) and water (20 mls) was then added dropwise at 0-5° C. The mixture was stirred for 10 minutes at 5° C. and then the temperature was slowly raised to and maintained at 90° C. for 1 hour. The reaction mixture was cooled to room temperature and sodium chloride added (30% w/v). The product was collected by filtration and washed with 20% sodium chloride solution. The dried product (56 g) contained 49% sodium chloride. Yield 74%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07446184B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-9dfec6ede0314f05884ce439909cfa27
Quellennotizuspto-grants-2008_11