(R)-(-)-alpha-methoxyphenylacetic acid → (R)-Cyclohexyl-methoxy-acetic acid
Reaktionsgleichung
[CH3:1][O:2][C@H:3]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:4]([OH:6])=[O:5]>CO>[CH:7]1([C@@H:3]([O:2][CH3:1])[C:4]([OH:6])=[O:5])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
An autoclave is charged with a solution of 1.00 g of (R)-α-methoxy-phenyl acetic acid in 20 ml methanol. 0.100 g of Nishimura catalyst are added and the mixture is hydrogenated at 4 bar and 20° C. for 1 hour. The mixture is filtered over Hyflo and the filtrate concentrated by evaporation to provide the title compound as a colourless oil. The crude material is used without further purification. Rf=0.84 (150:54:10:1 dichloromethane-methanol-water-acetic acid)
Aufarbeitung
- filtrationThe mixture is filtered over Hyflo
- concentrationthe filtrate concentrated by evaporation
Quellen und Nachweise
- ORD-Eintrag
- ord-1d5ad6911c144bbc9a2be7ac5df9d9ac
- Quelldatensatz
- uspto-grants-2010_08
- Patentnummer
- US07786307B2
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