HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5,6-Tetrafluorophthalic acid → 2,3,4,5-Tetrafluorobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5,6-Tetrafluorophthalic acid | HCID 69544 | — |
| Reactant | Calcium Hydroxide | HCID 6093208 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,4,5-Tetrafluorobenzoic acid | HCID 297549 | — |
Reaction Steps
Decarboxylation of 3,4,5,6-tetrafluorophthalic acid was carried out by following the procedure of Example 1, except that 238 g of 3,4,5,6-tetrafluorophthalic acid, 11.1 g (0.15 mole) of calcium hydroxide, and 480 g of water were used [pH 1.52 at 30° C. at the time of charging]. This example was found to have produced 2,3,4,5-tetrafluorobenzoic acid in a yield of 86.5 mole %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04769492 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-f4452561c35c40a3bf1eca29a46d71da |
| Source note | uspto-grants-1988_09 |