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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16123Erstellt: 23. Oktober 2026

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/de/reaction/16123

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktNitriteHCID 946—
EduktN,N-DimethylanilineHCID 949—
EduktN,N-Dimethyl-2-nitrosoanilineHCID 21646762—
ProduktHydrochloric AcidHCID 313—
ProduktN,N-dimethyl-p-phenylenediamineHCID 7472—

Reaktionsschritte

In step (a), nitrosodimethylaniline is prepared from dimethylaniline by treatment with nitrite (NaNO2) in aqueous acid (HCl) solution. In step (b), the nitroso compound is reduced to form p-aminodimethylaniline in aqueous acid (HCl) solution using zinc dust solution. In steps (c), (d), and (e), the p-aminodimethylaniline is oxidized in aqueous acid solution with another molecule of dimethylaniline, and simultaneously a thiosulfonic acid group is introduced; the ring is then closed using manganese dioxide or copper sulfate. More specifically, a clear neutral solution of p-aminodimethylaniline is acidified (H2SO4), and a non-reducing zinc chloride solution is added (ZnCl2 with Na2Cr2O7). Aluminium thiosulfate (Al2(S2O3)3) and sodium thiosulfate (Na2S2O3) are added. Sodium dichromate (Na2Cr2O7) is added. The mixture is heated and aerated. Dimethylaniline is added. Sodium dichromate (Na2Cr2O7) is added. The mixture is heated, and becomes dark greenish-blue in colour due to the formation of the thiosulfonic acid of Bindschedler green. Manganese dioxide or copper sulfate is added, and the mixture heated, and the dye precipitates from the concentrated zinc chloride solution.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737138B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3fca965c46274572b8aa89ab91bc72e0
Quellennotizuspto-grants-2010_06