Benzyl Bromide → HCID 67058419, Verbindung
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[OH:9].[CH2:10](Br)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2-bromo-5-chlorophenol (3.93 g, 18.94 mmol), benzyl bromide (3.42 g, 20 mmol) and potassium carbonate (10 g, 72.46 mmol) in acetone (80 ml) was stirred and refluxed for 3 hours then cooled, evaporated and dissolved in ether/water. The organic phase was dried (magnesium sulphate) evaporated and purified by chromatography on silica eluting with ethyl acetate/iso-hexane (1:99) to give 5.51 g of white solid.
Aufarbeitung
- temperaturerefluxed for 3 hours
- temperaturethen cooled
- customevaporated
- dissolutiondissolved in ether/water
- dry with materialThe organic phase was dried (magnesium sulphate)
- customevaporated
- custompurified by chromatography on silica eluting with ethyl acetate/iso-hexane (1:99)
Quellen und Nachweise
- ORD-Eintrag
- ord-d9292a6cf0e542dea94b01ff32c6b94e
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07446222B2
Notizen zur Reaktion
Wird geladen…