Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzene | HCID 241 | — |
| Edukt | Octane | HCID 356 | — |
| Edukt | Acetic acid, 2,2,2-trifluoro-, phenyl ester | HCID 68143 | — |
| Edukt | Trifluoroperacetic acid | HCID 10290812 | — |
| Katalysator | Cobalt diacetate | HCID 6277 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Trifluoroacetic acid | HCID 6422 | — |
| Produkt | Phenol | HCID 996 | — |
| Produkt | Acetic acid, 2,2,2-trifluoro-, phenyl ester | HCID 68143 | — |
Reaktionsschritte
To a solution of benzene (0.428 g. 5.49 mmol) and cobalt(II) acetate (0.179 g, 1.01 mmol) in 50 mL of trifluoroacetic acid/10% trifluoroacetic anhydride at 25° C. was added 10 mL of a 0.5 M solution of trifluoroperacetic acid in trifluoroacetic acid/10% trifluoracetic anhydride (cooled to 0° C.) by syringe pump over 20 h with stirring. The reaction mixture was initially a reddish-pink color which turned to dark green-black upon addition of the peracid. After the addition was complete, the reaction mixture was stirred an additional 7 h. then analyzed by gas chromatography using n-octane as an internal standard. The yield of phenyl trifluoroacetate was 56%, with a 58% conversion of benzene (selectivity to phenyl trifluoroacetate=96%) . Addition of water to the reaction mixture resulted in the quantitative conversion of phenyl trifluoroacetate to phenol and trifluoroacetic acid solvent.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04783550 |
|---|
| Quelldatensatz | uspto-grants-1988_11 |
|---|
| ORD ID | ord-62d1f9dd09984d8baa1efa63fd08253c |
|---|
| Quellennotiz | uspto-grants-1988_11 |
|---|