Reaktionsgleichung
[CH3:1][CH:2]([CH3:8])[CH2:3][CH2:4][C:5](Cl)=[O:6].[C:9]1([OH:15])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>O>[CH3:1][CH:2]([CH3:8])[CH2:3][CH2:4][C:5]([O:15][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4-Methylpentanoyl chloride (3.0 g, 22.3 mmol) was added dropwise to phenol (2.1 g, 22.3 mmol). After 3 hours, H2O was added and the reaction mixture was extracted with Et2O. The organic phase was washed with NaHCO3, then brine to neutrality, then dried (Na2SO4), concentrated and bulb-to-bulb distilled to afford the title compound in 88% yield.
Aufarbeitung
- extractionthe reaction mixture was extracted with Et2O
- washThe organic phase was washed with NaHCO3
- dry with materialbrine to neutrality, then dried (Na2SO4)
- concentrationconcentrated
- distillationbulb-to-bulb distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-2fdca11ac0de4538881cd3f7ef310dc2
- Quelldatensatz
- uspto-grants-2014_02
- Patentnummer
- US08648032B2
Verknüpfte Notizen
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