Acetic Acid → N-(4-ethyl-3-hydroxyphenyl)acetamide
Reaktionsgleichung
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11](=[O:13])[CH3:12])=[CH:6][C:5]=1[OH:14])(=O)[CH3:2].C(O)(=O)C>CO.[C].[Pd]>[CH2:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11](=[O:13])[CH3:12])=[CH:6][C:5]=1[OH:14])[CH3:2]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of N-(4-acetyl-3-hydroxyphenyl)acetamide (4.0 g, 20.7 mmol) in methanol (50 mL)/acetic acid (50 mL) was added 10% palladium-carbon powder (2.0 g), and the mixture was stirred at room temperature for 6 hr under a hydrogen atmosphere of 2.8 pressure. 10% Palladium-carbon powder was filtered off by celite filtration, the filtrate was concentrated under reduced pressure, and the obtained residue was washed with diisopropyl ether/hexane (1:1) to give the title compound (3.07 g, 83%) as a colorless powder.
Aufarbeitung
- filtration10% Palladium-carbon powder was filtered off by celite filtration
- concentrationthe filtrate was concentrated under reduced pressure
- washthe obtained residue was washed with diisopropyl ether/hexane (1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-95c18f9086b74881bbd45ef12846abd8
- Quelldatensatz
- uspto-grants-2013_01
- Patentnummer
- US08344135B2
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