Potassium Hydroxide → Cyclopropyl 4-fluorophenyl ketone
Reaktionsgleichung
Cl[CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=1)=[O:6].[OH-].[K+]>O>[CH:4]1([C:5]([C:7]2[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=2)=[O:6])[CH2:2][CH2:3]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Add 20.0 g (0.10 mole) γ-chloro-p-fluorobutyrophenone dropwise to a methanolic KOH solution (prepared from 9.8 g of 86% KOH pellets and 60 ml of methanol). Stir the mixture at room temperature for 40 minutes and pour into 100 ml of water and then extract with 3×30 ml of methylene chloride. Wash the methylene chloride extracts with 3×40 ml of water, dry over magnesium sulfate and evaporate off the solvent to provide the title compound.
Aufarbeitung
- extractionextract with 3×30 ml of methylene chloride
- washWash the methylene chloride
- dry with materialdry over magnesium sulfate
- customevaporate off the solvent
Quellen und Nachweise
- ORD-Eintrag
- ord-4cf3b9a24eff49e1960623cdd15230c5
- Quelldatensatz
- uspto-grants-1986_09
- Patentnummer
- US04613609
Notizen zur Reaktion
Wird geladen…