HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2,4-Dichlorobenzoic Acid → Tetrafluorophthalic anhydride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2,4-Dichlorobenzoic Acid | HCID 5787 | — |
| Edukt | Perfluoro-phthalide | HCID 11032047 | — |
| Edukt | 3,4,5,6-tetrafluorobenzene-1,2-dicarbonyl Fluoride | HCID 11075613 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | Tetrafluorophthalic anhydride | HCID 69545 | 72,05% |
Reaktionsschritte
Into a 300 ml glass reactor equipped with a reflux condenser and a stirrer, and 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, 59.3 g (0.31 mol) of 2,4-dichlorobenzoic acid and 100 ml of xylene were charged, and the mixture was reacted at 150° C. for 12 hours with vigorous stirring. Then, the reaction mixture was separated by distillation to obtain 32.8 g of tetrafluorophthalic anhydride. The yield was 72.05%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05523476 |
| Quelldatensatz | uspto-grants-1996_06 |
| ORD ID | ord-6fae364948344895bc9ed0136aec92eb |
| Quellennotiz | uspto-grants-1996_06 |