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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608914Generated: October 26, 2026

Phthalic Anhydride → HCID 131718923, compound

https://huagongshe.com/reaction/1608914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
Reactant6-Aminonaphthalene-1-sulphonic acidHCID 66470—
ReactantTriethylammoniumHCID 1385867—
ReactantSodium 6-aminonaphthalene-1-sulphonateHCID 23696805—
SolventPyridineHCID 1049—
ProductHCID 131718923HCID 131718923—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399487
Source datasetuspto-grants-1995_03
ORD IDord-05251847db624057a3846b096fcc6b76
Source noteuspto-grants-1995_03