Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,4,6-Trivinylboroxin-Pyridine Complex | HCID 2734806 | — |
| Edukt | 5-Acetyl-2-bromopyridine | HCID 15668195 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-(6-Vinylpyridin-3-YL)ethanone | HCID 59636720 | — |
Reaktionsschritte
The reaction mixture of 1-(6-bromopyridin-3-yl)ethanone (0.68 g, 3.41 mmol), 2,4,6-trivinyl-1,3,5,2,4,6-trioxatriborinane:pyridine (1:1) (0.57 g, 2.39 mmol), potassium carbonate (0.85 g, 6.14 mmol), and Pd(Ph3P)4 (0.16 g, 0.14 mmol) in acetonitrile (10 mL) was degassed with argon for 5 minutes. Then it was heated in the microwave for 30 min at 115° C. The organic phase was removed using a pipette, dried (MgSO4), filtered and concentrated and purified by flash chromatography (SiO2; heptane/EtOAc, gradient 20-80%). Yield: 0.36 g (72%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08859534B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-c90ffbba73da4c56b85a66e8591d4592 |
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| Quellennotiz | uspto-grants-2014_10 |
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