Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 2-Benzoylbenzaldehyde | HCID 161195 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | HCID 13195968 | HCID 13195968 | — |
| Katalysator | Pyridine | HCID 1049 | — |
| Katalysator | (Trimethylsilyl)methyl Trifluoromethanesulfonate [Trimethylsilylmethylating Reagent] | HCID 2760857 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(1,3-Dioxolan-2-YL)benzophenone | HCID 10515088 | — |
Reaktionsschritte
To a stirred solution of benzoylbenzaldehyde (2 g, 10 mmol) and 1,2-bis-(trimethoxysiloxy)ethane (2.3 g, 11 mmol) in dry dichloromethane (30 cm3) under N2 at room temperature was added trimethylsilylmethyl trifluoromethanesulphonate (5 drops). After stirring at 20° C. for 48 hours, pyridine (3 drops) was added followed by saturated NaHCO3 (20 cm3) and diethyl ether (20 cm3). The resulting mixture was stirred for 30 minutes. The ethereal layer was separated off and the aqueous layer extracted twice more with diethyl ether. The combined extracts were washed with water, dried over a mixture of anhydrous Na2CO3 and anhydrous Na2SO4 (1:1) and the solvent removed in vacuo to give 2-(3-benzoylphenyl)-1,3-dioxolane, nD20 1.5890. Yield 2.2 g (91.7%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04504491 |
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| Quelldatensatz | uspto-grants-1985_03 |
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| ORD ID | ord-2ae659d81b1c46e0943d7a38d3145739 |
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| Quellennotiz | uspto-grants-1985_03 |
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