Reaktionsgleichung
[CH:1]([Mg]Cl)=[CH2:2].[CH3:5][CH:6]([CH3:15])[CH2:7][CH2:8][C:9]1[C:10](=[O:14])[CH2:11][CH2:12][CH:13]=1>C(O)(=O)C>[CH3:5][CH:6]([CH3:15])[CH2:7][CH2:8][CH:9]1[CH:13]([CH:1]=[CH2:2])[CH2:12][CH2:11][C:10]1=[O:14]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- -25 °C
Versuchsvorschrift
Vinylmagnesium chloride (H2CHCClMg, 1 L) and cuprous chloride were charged to a dried flask under nitrogen and cooled to −25° C. with a dry ice bath. The resulting mixture was fed with 2-(3-methyl-butyl)-cyclopent-2-enone (226 g, 1.49 mol, obtained as detailed above) slowly for over 4 hours, aged for another 4 hours, and allowed to warm to 0° C. The reaction mixture was then poured into acetic acid solution and washed to neutral with saturated Na2CO3 solution. The distillation process provided the product 2-(3-methyl-butyl)-3-vinyl-cyclopentanone.
Aufarbeitung
- temperatureto warm to 0° C
- washwashed to neutral with saturated Na2CO3 solution
Quellen und Nachweise
- ORD-Eintrag
- ord-09352ae357f04cdba49ce68030613fe1
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09441185B2
Verknüpfte Notizen
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