Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Anisole | HCID 7519 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Katalysator | Scandium | HCID 23952 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Nitromethane | HCID 6375 | — |
| Produkt | 4'-Methoxyacetophenone | HCID 7476 | 97,2% |
Reaktionsschritte
The catalytic effect of the scandium salt of 5-trifluoromethanesulfonyl-1,3-dibutyl-2-sulfonyl-barbituric acid, obtained in Example 25, towards a Friedel-Crafts reaction of acylation was evaluated in the following manner. In 40 ml of anhydrous nitromethane, there is added 887 mg (0.7 moles) of the scandium salt of 5-trifluoromethylsulfonyl-1,3-dibutyl-2-sulfonyl-barbituric acid, and 1.08 g (10 mmoles) of anisole and 2.04 g (20 mmoles) of acetic anhydride. After stirring during 10 min at 21° C., the reaction mixture was diluted with 50 ml of ether and the reaction was inhibited with 100 ml of a saturated solution of sodium bicarbonate NaHCO3. After filtration on Celite, the solution was extracted with three fractions of 50 ml ether, then the collected ether phase was washed with a saturated solution of potassium chloride. After drying the ether phase with magnesium sulfate and evaporation, 1.46 g of p-methoxyacetophenone (95% yield) were recovered with a purity characterized by a proton RMN higher than 99%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06171522B2 |
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| Quelldatensatz | uspto-grants-2001_01 |
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| ORD ID | ord-fa95fa811c2545e2a80299e9984faeaf |
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| Quellennotiz | uspto-grants-2001_01 |
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