HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Tetrafluorophthalic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3,4,5,6-tetrafluorobenzene-1,2-dicarbonyl Fluoride | HCID 11075613 | — |
| Product | Tetrafluorophthalic anhydride | HCID 69545 | 73.5% |
Reaction Steps
Into a 300 ml glass reactor equipped with a reflux condenser and a stirrer, 100 g (0.413 mol) of the 3,4,5,6-tetrafluorophthaloyldifluoride separated by distillation from the mixture of Example 2, and 100 ml of acetic acid were charged, and the mixture was reacted at 130° C. for 1.5 hours with vigorous stirring. Then, the inorganic substance was removed by filtration, and the residue was separated by distillation to obtain 66.8 g of tetrafluorophthalic anhydride. The yield was 73.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05648504 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-f3a51d275aca4c63b5a228d4ad605f69 |
| Source note | uspto-grants-1997_07 |