Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium fluoride | HCID 25953 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | Benzene, 1-bromo-3,5-dimethyl- | HCID 136357 | — |
| Edukt | HCID 178419127 | HCID 178419127 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Katalysator | 2,2'-Bis(dicyclohexylphosphino)-1,1'-binaphthyl | HCID 4368621 | — |
| Produkt | 3,5-Dimethylbiphenyl | HCID 86927 | 94% |
Reaktionsschritte
An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1 mol %), ligand 2 [Example 1] (5.9 mg, 0.015 mmol, 1.5 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), and cesium fluoride (456 mg, 3.0 mmol). The tube was purged with argon, and dioxane (3 mL) and 5-bromo-m-xylene (0.135 mL, 1.0 mmol) were added through a rubber septum. The septum was removed, the tube was sealed with a teflon screw cap and the mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (20 mL) and poured into a separatory funnel. The mixture was washed with 1M NaOH (20 mL), and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was then purified by flash chromatography on silica gel to give 171 mg (94%) of a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07560582B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-03db3cf90ed441c4aa4f64d227ab0f4c |
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| Quellennotiz | uspto-grants-2009_07 |
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