Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443731Generated: October 25, 2026

Sodium Chloride → 1-Hydroxynaphthalene-4,6-disulphonic acid

https://huagongshe.com/reaction/443731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant2-Aminobenzenesulfonic acidHCID 6926—
ReactantSodium SulfideHCID 14804—
Reactant1-(4'-Nitrophenylamino)-8-hydroxynaphthalene-3,6-disulphonic acidHCID 23465233—
Product1-Hydroxynaphthalene-4,6-disulphonic acidHCID 12284354—

Reaction Steps

6.8 parts of 2,4,6-trifluoro-1,3,5-triazine are added dropwise to a solution of 13.4 parts of 1,4-diaminobenzene-2,5-disulphonic acid in 200 parts by volume of water at 0° C. and a pH value of 4 to 5 is maintained by constantly neutralising the hydrogen fluoride liberated. The course of the reaction is followed chromatographically. The resulting solution of the intermediate product is condensed, at a pH value of 7 to 8 and at 10° to 20° C. with 31 parts of the aminoazo dyestuff obtained by coupling diazotised 1-aminobenzene-2-sulphonic acid with 1-(4'-nitrophenylamino)-8-hydroxynaphthalene-3,6-disulphonic acid and subsequently reducing the nitro group with sodium sulphide. The dyestuff is salted out completely with sodium chloride, filtered off, washed and again converted to a neutral solution in 500 parts by volume of water. Further diazotisation of the resulting aminoazo dyestuff and coupling with 15 parts of 1-hydroxynaphthalene-4,6-disulphonic acid gives the dyestuff of the formula ##STR43## which is precipitated with sodium chloride, isolated and then washed and dried. It is a dark red powder which gives a red solution in water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261889
Source datasetuspto-grants-1981_04
ORD IDord-7a2f504082914162aa6b1e8fdc6ad59a
Source noteuspto-grants-1981_04