Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Butanol | HCID 263 | — |
| Edukt | Cyclohexanone | HCID 7967 | — |
| Edukt | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Katalysator | Bismuth trichloride | HCID 24591 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1,1-Dibutoxycyclohexane | HCID 243718 | 182,2% |
Reaktionsschritte
In a 300-ml three-necked flask, 98 g of cyclohexanone, 148 g of n-butanol, 50 g of anhydrous magnesium sulfate, 2 mg of bismuth chloride and 80 g of toluene were charged. The resulting mixture was stirred at 10° C. under atmospheric pressure for 10 hours in a nitrogen atmosphere. After magnesium sulfate was removed from the reaction mixture, the solvent (toluene) and unreacted starting materials were distilled off under reduced pressure. Distillation of the residue under reduced pressure gave 207.7 g of cyclohexanone dibutyl acetal (yield: 89.4%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05792876 |
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| Quelldatensatz | uspto-grants-1998_08 |
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| ORD ID | ord-b875a7393a85409cb8f86ed45dbcfed7 |
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| Quellennotiz | uspto-grants-1998_08 |
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