Boron tribromide → 3-Chloro-2-fluoro-6-hydroxybenzaldehyde
Reaktionsgleichung
[Cl:1][C:2]1[C:3]([F:12])=[C:4]([C:7]([O:10]C)=[CH:8][CH:9]=1)[CH:5]=[O:6].B(Br)(Br)Br>ClCCl>[Cl:1][C:2]1[C:3]([F:12])=[C:4]([C:7]([OH:10])=[CH:8][CH:9]=1)[CH:5]=[O:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 3-chloro-2-fluoro-6-methoxy-benzaldehyde (10 g, 53.2 mmol,) in dichloromethane (200 mL) at −78° C. was added a dichloromethane solution (1 M) of BBr3 (159 mL, 159 mmol) dropwise. The mixture was gradually warmed to room temperature and stirred for 1 h, then quenched with water. The mixture was extracted with dichloromethane three times. The organic layer were combined, washed with brine, dried over MgSO4, concentrated to give a residue. The reside was triturated with dichloromethane and hexanes to afford 3-chloro-2-fluoro-6-hydroxy-benzaldehyde as a brown solid (Yield: 2.07 g, 22%)
Aufarbeitung
- customquenched with water
- extractionThe mixture was extracted with dichloromethane three times
- washwashed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated
- customto give a residue
- customThe reside was triturated with dichloromethane and hexanes
Quellen und Nachweise
- ORD-Eintrag
- ord-89e76eaa207b45609c87dda350f7d0f9
- Quelldatensatz
- uspto-grants-2012_03
- Patentnummer
- US08134001B2
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