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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 268233Erstellt: 24. Oktober 2026

Hydroquinone → p-Dihydroxy benzene disulfonic acid

https://huagongshe.com/de/reaction/268233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroquinoneHCID 785—
EduktSulfuric AcidHCID 1118—
Edukt1,4-DioxaneHCID 31275—
LösungsmittelTetrachloroethyleneHCID 31373—
Produktp-Dihydroxy benzene disulfonic acidHCID 21124945139%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

190 g of p-dihydroxy benzene monosulfonic acid, 100 ml of dioxane, and 100 ml of perchloroethylene are mixed in a flask provided with a reflux condenser. The flask is heated in an oil bath to the reflux temperature (in the oil bath at 140°C). It is refluxed for half an hour, and then is left to cool a little to set the coolant for distillation. In the flask, two layers are formed: a colourless lower layer, and a coloured upper layer in which the acid is dissolved. The flask is heated again and 100 ml of the solvent mixture are distilled. In the mixture collected, two layers form, the upper, moderate, is aqueous. To the flask provided with a reflux condenser, 98 g of sulfuric acid containing 20 % of SO3 are added, and it is heated again, to a lower temperature, so that the reflux is barely noticeable (bath temperature: 130°C), for four hours. The liquids accompanying the acid are removed by distilling at reduced pressure, the residue is dissolved in a little water, 2 g of active charcoal are added, and it is filtered. The solution is concentrated, cooled, and is precipitated by adding five volumes of acetone. The precipate is filtered, and 189 g of p-dihydroxy benzene disulfonic acid, with a melting point of 166° - 169°C are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03947448
Quelldatensatzuspto-grants-1976_03
ORD IDord-521c9407e4a64a9ca0c93b936b9cd4bd
Quellennotizuspto-grants-1976_03