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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1608914Erstellt: 27. Oktober 2026

Phthalic Anhydride → HCID 131718923, Verbindung

https://huagongshe.com/reaction/1608914

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalic AnhydrideHCID 6811—
Edukt6-Aminonaphthalene-1-sulphonic acidHCID 66470—
EduktTriethylammoniumHCID 1385867—
EduktSodium 6-aminonaphthalene-1-sulphonateHCID 23696805—
LösungsmittelPyridineHCID 1049—
ProduktHCID 131718923HCID 131718923—

Reaktionsschritte

223 g (1 mol) of 6-amino-1-naphthalenesulfonic acid and 148 g (1 mol) of phthalic anhydride are boiled for 0.5 h in 1 liter of pyridine. After boiling, the reaction mixture is left at room temperature for 16 h. The precipitated product is filtered and washed with pyridine and water, and then recrystallized from boiling water. Yield 298 g (69%); mp 234°-237° C.; Anal. Calcd. for C23H16N2SO5 :C 63.88, H 3.73, N 6.48, S 7.42; Found:C 63.74, H 3.81, N 6.52, S 6.99. When the 6-phthalimido-1-naphthalenesulfonic acid pyridinium salt was synthesized starting from 6-amino-1-naphthalenesulfonic acid sodium salt or triethylammonium salt, the calculated yields were 63% and 58% respectively.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05399487
Quelldatensatzuspto-grants-1995_03
ORD IDord-05251847db624057a3846b096fcc6b76
Quellennotizuspto-grants-1995_03