Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Trimethylsilyl triflate | HCID 65367 | — |
| Edukt | 5-Bromo-2-iodo-1,3-dimethylbenzene | HCID 2735573 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 3,5-Dimethyl-4-trimethylsilylbromobenzene | HCID 23071693 | 85% |
Reaktionsschritte
2,6-Dimethyl-4-bromoiodobenzene (5.04 g, 16.2 mmol) was dissolved in diethyl ether (50 ml). To the solution was then added dropwise a hexane solution of n-butyl lithium (2.6 M, 6.5 ml) at −50° C. The mixture was then stirred at the same temperature for 45 minutes. To the mixture was then added dropwise trimethylsilyl trifluoromethanesulfonate (3.7 ml, 19.4 mmol). The mixture was then stirred at −30° C. for 30 minutes and at room temperature overnight. After the quenching of the reaction with water, the product was then extracted with diethyl ether. The resulting organic phase was then dried over magnesium sulfate. The solvent was then distilled off. The crude product thus obtained was then distilled under reduced pressure using a glass tube oven so that it was purified to obtain 3,5-dimethyl-4-trimethylsilylbromobenzene (3.54 g; yield: 85%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07189790B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-a2c939712ae74679a0a34cfd7765bb4f |
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| Quellennotiz | uspto-grants-2007_03 |
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