HuagongsheHuagongshe Chemistry Print Report · For research reference only
Perfluoro-phthalide → Tetrafluorophthalic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Perfluoro-phthalide | HCID 11032047 | — |
| Reactant | 3,4,5,6-tetrafluorobenzene-1,2-dicarbonyl Fluoride | HCID 11075613 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Tetrafluorophthalic anhydride | HCID 69545 | 64.3% |
Reaction Steps
Into a 200 ml glass reactor equipped with a reflux condenser and a stirrer, 50 g (0.207 mol) of the mixture (1:1) of the 3,4,5,6-tetrafluorophthaloyldifluoride and the 3,3,4,5,6,7-hexafluoro-1-[3H]-isobenzofuranone of Example 2, and 50 ml of acetic acid were charged, and the mixture was refluxed for 16 hours with vigorous stirring. Then, the reaction mixture was separated by distillation to obtain 29.3 g of tetrafluorophthalic anhydride. The yield was 64.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05523476 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-229d9eed8e8d4ae0bb94ab5bc572ceb6 |
| Source note | uspto-grants-1996_06 |