Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704197Generated: November 1, 2026

H acid → 2-Aminobenzenesulfonic acid

https://huagongshe.com/reaction/1704197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantH acidHCID 7009—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-5-(aminomethyl)naphthalene-1-sulphonic acidHCID 104072—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Product2-Aminobenzenesulfonic acidHCID 6926—

Reaction Steps

The diazotisation product prepared according to the instructions of Example 3 from 36.5 parts of 2-amino-1-sulpho-5-aminomethyl-naphthalene is mixed with a neutral solution of 46 parts of 1-hydroxy-8-amino-3,6-disulphonaphthalene. To accelerate the coupling, the mixture is buffered to pH 2 by adding sodium acetate solution. The acid coupling is complete after stirring for several hours. The dyestuff solution is neutralised with sodium hydroxide solution. 40 parts of sodium bicarbonate and a little CaO are added and the diazotisation product obtained from 25 parts of o-sulphanilic acid is then added. The disazo dyestuff is separated out by adding salt. The paste is stirred into 1,000 parts by volume of water. 16 parts by volume of 2,4,6-trifluoro-5-chloro-pyrimidine are added dropwise at 15° and pH 8.5. The pH is kept at 8.5 by simultaneous addition of 2 N sodium hydroxide solution. After completion of the acylation, the dyestuff is salted out, dried and ground. An easily water-soluble black dyestuff powder is obtained. In the form of the free acid, the dyestuff corresponds to the structure: ##STR22##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126609
Source datasetuspto-grants-1978_11
ORD IDord-290ebb751b22420898e09f036f26f099
Source noteuspto-grants-1978_11