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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197210Generated: October 26, 2026

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

https://huagongshe.com/reaction/1197210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantDimethyl SulfateHCID 6497—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant2,4-Diaminobenzenesulfonic acidHCID 66623—
SolventFormic AcidHCID 284—
SolventWaterHCID 962—
Product3-(N-methylamino)aniline-4-sulfonic acidHCID 10965570—

Reaction Conditions

Temperature20 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05117050
Source datasetuspto-grants-1992_05
ORD IDord-d46403aea0164f58b488fbb708d4e92a
Source noteuspto-grants-1992_05