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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1197210Erstellt: 26. Oktober 2026

Hydrochloric Acid → 3-(N-methylamino)aniline-4-sulfonic acid

https://huagongshe.com/reaction/1197210

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium ChlorideHCID 5234—
EduktDimethyl SulfateHCID 6497—
EduktAcetic AnhydrideHCID 7918—
EduktSodium HydroxideHCID 14798—
Edukt2,4-Diaminobenzenesulfonic acidHCID 66623—
LösungsmittelFormic AcidHCID 284—
LösungsmittelWaterHCID 962—
Produkt3-(N-methylamino)aniline-4-sulfonic acidHCID 10965570—

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

94 g of 1,3-diaminobenzene-4-sulfonic acid in 430 ml of water and 70 g of formic acid were boiled for 3 hours under reflux. The mixture was cooled to 20° C., and the resulting 3-(N-formylamino)aniline-4-sulfonic acid was filtered off in vacuo and stirred in 500 g of water with the addition of caustic soda solution to give a pH of 6.5. 70 g of acetic anhydride were then added and the pH was kept between 5.0 and 6.5 by the addition of caustic soda solution. After 30 minutes, the pH was adjusted to 12.5 with caustic soda solution, and 75 g of dimethyl sulfate were added dropwise. After 30 minutes, the pH was adjusted to -0.5 with hydrochloric acid, and the mixture was boiled under reflux for 3 hours. After cooling, the mixture was adjusted to pH 1.0 with caustic soda solution and salted out with 150 g of sodium chloride. The precipitated 3-(N-methylamino)aniline- 4-sulfonic acid was isolated by filtration in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05117050
Quelldatensatzuspto-grants-1992_05
ORD IDord-d46403aea0164f58b488fbb708d4e92a
Quellennotizuspto-grants-1992_05