(5-Benzyloxy-2-chloro-phenyl)-acetic acid ethyl ester → (2-Chloro-5-hydroxy-phenyl)-acetic acid ethyl ester
Reaktionsgleichung
[CH2:1]([O:3][C:4](=[O:21])[CH2:5][C:6]1[CH:11]=[C:10]([O:12]CC2C=CC=CC=2)[CH:9]=[CH:8][C:7]=1[Cl:20])[CH3:2]>CCO>[CH2:1]([O:3][C:4](=[O:21])[CH2:5][C:6]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:7]=1[Cl:20])[CH3:2]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
(5-Benzyloxy-2-chloro-phenyl)-acetic acid ethyl ester (1.7 g, 5.6 mmol) was dissolved in EtOH (30 mL) and degassed with N2. 5% Palladium on carbon (1 g) was added, and the reaction was purged with H2 and then stirred under an H2 balloon at 50° C. overnight. The mixture was filtered and concentrated to give the title compound.
Aufarbeitung
- customdegassed with N2
- addition5% Palladium on carbon (1 g) was added
- customthe reaction was purged with H2
- filtrationThe mixture was filtered
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-216a9f7ab45f4094902afe2ce462aada
- Quelldatensatz
- uspto-grants-2013_01
- Patentnummer
- US08362044B2
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