Reaktionsgleichung
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH2:6][CH2:7][C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.[OH-].[K+].[CH2:15](Br)[CH:16]=[CH2:17].O>C(O)C>[CH2:17]([O:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][CH2:7][C:8](=[O:10])[CH3:9])=[CH:11][CH:12]=1)[CH:16]=[CH2:15]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
p-Hydroxy benzylacetone (1.5 g.), KOH (6 g.) and allyl bromide (1.2 g.) were stirred in ethanol (50 ml) overnight. Water was added and the mixture extracted with ether, which was evaporated to give the compound (1.6 g.) as an oil purified by column chromatography.
Aufarbeitung
- extractionthe mixture extracted with ether, which
- customwas evaporated
- customto give the compound (1.6 g.) as an oil
- custompurified by column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-67502816a83c4a06a3fe4d307df71c29
- Quelldatensatz
- uspto-grants-1977_12
- Patentnummer
- US04062978
Verknüpfte Notizen
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