Ethyl bromoacetate → Ethyl 2-(5-chloro-2-methoxyphenoxy)acetate
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([OH:8])[CH:7]=1.C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]>CC(C)=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH3:10])=[C:6]([CH:7]=1)[O:8][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 5-chloro-2-methoxyphenol (488 mg) in acetone (15 ml) were added cesium carbonate (1.20 g) and ethyl bromoacetate (375 μl), and the mixture was stirred for 1 hour at room temperature. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. Purification of the residue by flash column chromatography on silica gel (eluent: hexane/ethyl acetate=6/1) gave ethyl 2-(5-chloro-2-methoxyphenoxy)acetate (572 mg).
Aufarbeitung
- filtrationThe insoluble material was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- customPurification of the residue by flash column chromatography on silica gel (eluent: hexane/ethyl acetate=6/1)
Quellen und Nachweise
- ORD-Eintrag
- ord-6bb59a5168c14f8da619c4cdbac83b5c
- Quelldatensatz
- uspto-grants-2003_03
- Patentnummer
- US06538152B1
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