HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 131718923, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 6-Aminonaphthalene-1-sulphonic acid | HCID 66470 | — |
| Reactant | Triethylammonium | HCID 1385867 | — |
| Reactant | Sodium 6-aminonaphthalene-1-sulphonate | HCID 23696805 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 131718923 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399487 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-05251847db624057a3846b096fcc6b76 |
| Source note | uspto-grants-1995_03 |