Reaktionsgleichung
[F:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[Br:11]Br>C(O)(=O)C>[Br:11][C:7]1[C:8]([OH:10])=[CH:9][C:2]([F:1])=[C:3]([CH:6]=1)[CH:4]=[O:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 45 °C
Versuchsvorschrift
To a solution of 2-fluoro-4-hydroxybenzaldehyde (2.2 g, 15.7 mmol, 1 eq) in acetic acid (70 mL) was added a solution of bromine (2.71 g, 17.0 mmol, 1.1 eq) in acetic acid (10 mL), and the mixture was stirred at 45° C. for 26 h. The reaction was concentrated in vacuo, brine (50 mL) was added, and the mixture was extracted with EtOAc (3×80 mL). The combined organic layers were dried (Na2SO4), concentrated in vacuo. The resultant residue was purified by silica gel chromatography (DCM:MeOH=15:1 to 5:1) to afford 1.2 g (35%) of 5-bromo-2-fluoro-4-hydroxybenzaldehyde (25).
Aufarbeitung
- concentrationThe reaction was concentrated in vacuo, brine (50 mL)
- additionwas added
- extractionthe mixture was extracted with EtOAc (3×80 mL)
- dry with materialThe combined organic layers were dried (Na2SO4)
- concentrationconcentrated in vacuo
- customThe resultant residue was purified by silica gel chromatography (DCM:MeOH=15:1 to 5:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-86b166b84f3a4470880b3752f6023d13
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08822467B2
Verknüpfte Notizen
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