Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloride | HCID 312 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | 4-Butylbenzaldehyde | HCID 70988 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Produkt | 2-(4-Butylphenyl)-1-methoxyethene | HCID 54090937 | — |
Reaktionsschritte
21.1 g of methoxymethyltriphnylphosphonium chloride is introduced into 280 ml of diethyl ether under nitrogen. At 0° C., 29.6 ml of n-butyllithium solution (1.6 M in hexane) is added in drops, and it is stirred for one hour at room temperature. 10 g of 4-butylbenzaldehyde in 40 ml of diethyl ether is now added, and it is stirred for one more hour. Sodium chloride solution is added to the reaction mixture, extracted with ethyl acetate, dried on sodium sulfate and concentrated by evaporation. After chromatography on silica gel with ethyl acetate, 6.7 g of 2-(4-butylphenyl)-1-methoxyethene 48 (E,Z-mixture) is obtained as a colorless oil, which is dissolved in 200 ml of acetone and is stirred under nitrogen with 10 ml of 2N hydrochloric acid overnight. Sodium chloride solution is added, extracted with ethyl acetate, dried on sodium sulfate and concentrated by evaporation. Chromatographic purification on silica gel with ethyl acetate/hexane yields 3.9 g of title compound 49 as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07211680B2 |
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| Quelldatensatz | uspto-grants-2007_05 |
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| ORD ID | ord-57a7b244cb264c7f9a0456e34f2401d2 |
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| Quellennotiz | uspto-grants-2007_05 |
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