HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Tetrafluorophthalic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4,5,6,7-Tetrafluoro-2-(propan-2-yl)-1H-isoindole-1,3(2H)-dione | HCID 14274183 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tetrafluorophthalic anhydride | HCID 69545 | 66.4% |
Reaction Steps
In a 500 ml three neck distillation flask were placed 47 g (0.18 mol) of N-isopropyl-tetrafluorophthalimide, 71 ml of concentrated sulfuric acid, 43 ml of acetic acid, and 13 ml of water, and the mixture was reacted for 5 hours at 140° to 150° C. with stirring. After cooling, the reaction mixture was extracted three times with 200 ml of toluene, and the toluene layers thus formed were collected and concentrated by distillation under a reduced pressure to provide 26.3 g (yield 66.4%) of tetrafluorophthalic anhydride as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04769493 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-47d579934062463994cdee766542ddea |
| Source note | uspto-grants-1988_09 |