HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129532Erstellt: 24. Oktober 2026
Cyclododecanecarboxaldehyde → 1-(3-Phenyl-1-propenyl)cyclododecane
https://huagongshe.com/de/reaction/129532
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cyclododecanecarboxaldehyde | HCID 78737 | — |
| Edukt | Phenethyltriphenylphosphonium bromide | HCID 10863251 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1-(3-Phenyl-1-propenyl)cyclododecane | HCID 54471716 | 88,2% |
Reaktionsschritte
To 11.4 g (25.5 mmol) of phenylethyl triphenylphosphonium bromide in 50 mL of dry ether at 0° C. is added 10.2 mL (25.5 mmol) of 2.5M butyllithium. The suspension is stirred at 0° C. for 1 hour followed by the addition of 5.0 g (25.5 mmol) of cyclododecane carboxaldehyde. The mixture is stirred at room temperature for 3 hours after which time no starting material is evident by TLC. The reaction mixture is quenched with 1N HCl. The layers are separated and the aqueous layer is washed twice with ethyl ether. The combined organic layers are dried over a MgSO4 and the ether is evaporated. The residue is flash chromatographed on silica gel using hexanes to give 6.4 g of a colorless oil: NMR (CDCl3) δ 1.0-1.6 (m, 10H), 2.6 (m, 1H), 3.4 (d, 2H, J=8 Hz,), 5.3 (t, 1H, J=7 Hz), 5.45 (q, 1H, J=7 Hz), 7.2 ppm (m, 5
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05468774 |
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| Quelldatensatz | uspto-grants-1995_11 |
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| ORD ID | ord-c1a0464607584b3bbe40ecd0acae5021 |
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| Quellennotiz | uspto-grants-1995_11 |
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