HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1639951Erstellt: 26. Oktober 2026
tert-Butylphosphine → 3-(4'-Vinyl-biphenyl-3-yl)pyridine
https://huagongshe.com/reaction/1639951
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butylphosphine | HCID 123165 | — |
| Edukt | 4-Vinylphenylboronic acid | HCID 2734393 | — |
| Edukt | 3-(3-Chlorophenyl)pyridine | HCID 14921465 | — |
| Edukt | HCID 178506427 | HCID 178506427 | — |
| Katalysator | Tris(dibenzylideneacetone) palladium | HCID 44556509 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 3-(4'-Vinyl-biphenyl-3-yl)pyridine | HCID 66722408 | 45% |
Reaktionsschritte
This Example was carried out in the same manner as Example 10, except that 23.42 g (0.158 mol) of 4-vinyl-phenyl boronic acid, 20.0 g (0.1055 mol) of 3-(3-chloro-phenyl)pyridine, 500□ of 1,4-dioxane, 27.54 g (0.474 mol, 3.3 equivalent) of fluoro-potassium, 1.69 g (0.0084 mol, 5.3 mol %) of t-butylphosphine [P( t-Bu)3)], and 2.6 g (0.0028 mol, 1.8 mol %) of palladium tris(dibenzylidene acetone) [Pd2(dba)3] were used. Finally, after the resulting solution was heated to reflux at 80° C. for 24 hours, the 3-(4′-vinyl-biphenyl-3-yl)pyridine was isolated. The yield was 45%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08110642B2 |
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| Quelldatensatz | uspto-grants-2012_02 |
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| ORD ID | ord-77f85fe9188b4299b205d56d69559d9a |
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| Quellennotiz | uspto-grants-2012_02 |
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