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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2072329Erstellt: 26. Oktober 2026

Hydrochloric Acid → 5-(3-Phosphonoanilino)naphthalene-2-sulfonic acid

https://huagongshe.com/reaction/2072329

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSulfur DioxideHCID 1119—
Edukt1,6-Cleve's acidHCID 8408—
EduktSodium HydroxideHCID 14798—
EduktPhosphonic acid, P-(3-aminophenyl)-HCID 79477—
EduktSodium BisulfiteHCID 23665763—
Produkt5-(3-Phosphonoanilino)naphthalene-2-sulfonic acidHCID 21408081—

Reaktionsschritte

Sodium bisulphite liquor (40% -- 23 parts), sodium hydroxide liquor (70° Tw -- 8.1 parts), salt (1.8 parts), 1-amino-6-sulphonaphtalene (11.2 parts) and 3-aminophenylphosphonic acid (10.4 parts) are heated in a sealed tube for 10 hours at 130° C. After cooling the tube is opened and hydrochloric acid (36% - 13.9 parts) is added until an acid reaction is obtained on Congo Red paper. The suspension is boiled under reflux for 1 hour until evolution of sulphur dioxide has essentially ceased. During this period samples are spotted on to Congo Red paper to confirm acid reaction. The suspension is cooled to room temperature and filtered. The filtrate is set stirring and sodium chloride (8 parts = 20% wt/vol) added. After stirring for 18 hours the suspension is filtered under vacuum and the cake pressed well to remove mothers liquor. The paste (8 parts) is dried in air at 50°-60° C to give 7 parts of 1-(3-phosphonophenylamino)-6-sulphonaphthalene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04051175
Quelldatensatzuspto-grants-1977_09
ORD IDord-2d05a617a8a2480e83c823609123cfe6
Quellennotizuspto-grants-1977_09