Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Triethylsilane | HCID 12052 | — |
| Edukt | 3,4-Dimethoxystyrene | HCID 61400 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 4-Ethyl-1,2-dimethoxybenzene | HCID 79990 | 57% |
Reaktionsschritte
In a 5 mL flask opened to the air, to a clear solution of 3,4-dimethoxystyrene (100 μL, 0.755 mmol) in benzene (0.8 mL) was added triethylsilane (240 μL, 0.816 mmol). The flask was placed in a 60° C. bath and iodo[bis(triphenylphosphine)]dioxorhenium(V) (32 mg, 0.037 mmol) was added. The resulting brown solution was heated at 60° C. for 12 hours. The crude reaction mixture was directly applied to a SiO2 column and chromatographed eluting with 4:1 hexanes:diethyl ether to afford 3,4-dimethoxyethylbenzene (52 mg, 57% yield) as a colorless liquid. The reaction was repeated using pent-2-enal and t-butyl acrylate as the electrophilic reactants, as indicated in the first two schemes above (wherein “TES” represents triethylsilyl).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07262315B2 |
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| Quelldatensatz | uspto-grants-2007_08 |
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| ORD ID | ord-8aadcf4acfbb4971aadb87d91ca5d5c6 |
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| Quellennotiz | uspto-grants-2007_08 |
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