HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53564Erstellt: 23. Oktober 2026
2-Pyridinecarboxaldehyde → E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene
https://huagongshe.com/de/reaction/53564
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Edukt | 2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide | HCID 2724168 | — |
| Edukt | 3-(1,3-Dioxan-2-yl)-1-(2-pyridyl)-1-propene | HCID 53923275 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene | HCID 19694130 | — |
| Produkt | Z-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene | HCID 70113689 | — |
Reaktionsschritte
(E and Z)-3-(1,3-Dioxan-2-yl)-1-(2-pyridyl)-1-propene (148 and 149). To a suspension of 4.6 g (10.2 mmol) of [2-(1,3-dioxan-2-yl)ethyl]triphenylphosphonium bromide (Aldrich Chemical Co.) in 50 mL of THF at 0° C. was added 6.4 mL (10.2 mmol) of n-butyl lithium (1.6M in hexanes) and the resulting red solution was allowed to stir at 0° C. for 0.5 h. To this solution was added 880 μL (9.3 mmol) of 2-pyridinecarboxaldehyde (Aldrich Chemical Co.). The reaction mixture was allowed to stir at room temperature for 1 h and was then poured into water and partitioned with ether. The combined either extracts were dried over MgSO4 and concentrated. Flash chromatography (elution with 3:1 hexane:ethyl acetate) gave 0.43 g of E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1 -propene (148) and 1.12 g of Z-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene (149). 1H NMRs consistent with structures.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05620971 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-321cdd4893b44debad54cad867cbe1e8 |
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| Quellennotiz | uspto-grants-1997_04 |
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