Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH:9]=[O:10])=[CH:4][CH:3]=1.S(=O)(=O)(O)[OH:12].Cl[O-].[Na+]>>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:12])=[O:10])=[CH:4][CH:3]=1Komponenten
4
Versuchsvorschrift
In the like manner as Example 1, 26.4 g of p-methylphenylacetaldehyde as an aldehyde and 2.3 g of sulfuric acid were used. The oxidation was done by using 125 g of 12% aqueous solution of sodium hypochlorite at temperatures of -10° to -12° C., which was followed by the hydrogenation to obtain p-methylphenylacetic acid.
Aufarbeitung
- customat temperatures of -10° to -12° C., which
Quellen und Nachweise
- ORD-Eintrag
- ord-a6c0e22ac83543e18b5dba56bc8d265d
- Quelldatensatz
- uspto-grants-1989_03
- Patentnummer
- US04814494
Verknüpfte Notizen
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