Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tert-Butylhydroquinone | HCID 16043 | — |
| Katalysator | HCID 178418406 | HCID 178418406 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | tert-Butyl-1,4-benzoquinone | HCID 19211 | 80% |
Reaktionsschritte
16.6 g (0.10 mol) of 2-tert-butylhydroquinone was placed in a 200 cc 3-neck flask. After adding 17.4 g (0.20 mol) of powdery manganese dioxide, 100 cc of toluene was added thereto, and the mixture was heated with stirring. The temperature was maintained at 70° C. for 3 hours. After cooling to room temperature, the manganese dioxide was removed by filtration by means of suction using Celite as a filter aid. Then the manganese dioxide was washed with 50 cc of toluene, and the toluene was evaporated to dryness, by which 2-tert-butyl-1,4-benzoquinone was obtained. The yield was 80% and the melting point was 48°-50° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04345016 |
|---|
| Quelldatensatz | uspto-grants-1982_08 |
|---|
| ORD ID | ord-5837863e67dc4d6886cf275d938e21dc |
|---|
| Quellennotiz | uspto-grants-1982_08 |
|---|