4-Isopropylbenzoic Acid → 4-(2-Hydroxypropan-2-yl)benzoic acid
Reaktionsgleichung
[CH:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[CH:6][CH:5]=1)([CH3:3])[CH3:2].[Mn]([O-])(=O)(=O)=[O:14].[K+]>[OH-].[K+].O.OCC(CO)O>[OH:14][C:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[CH:6][CH:5]=1)([CH3:3])[CH3:2]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
4-Isopropyl-benzoic acid (5.00 g, 30.0 mmol) was dissolved in 20 mL of 10% potassium hydroxide in water solution. To this solution was added 480 mL of 0.2 N aqueous potassium hydroxide solution, followed by a solution of potassium permanganate (9.65 g, 60.0 mmol) in 500 mL of water. The mixture was stirred at 70° C. for one hour. To the reaction mixture was added a few drops of glycerol, and the resulting mixture was cooled to 0° C. Solid residues were removed by filtration, and the filtrate was acidified to pH 1 and extracted twice with ether. The ether extracts were combined, rinsed once with brine and dried over magnesium sulfate and concentrated in vacuo. The concentrate was washed with carbon tetrachloride and recrystallized from water to give 2.2 g (12.2 mmol) of 4-(1-hydroxy-1-methyl-ethyl)-benzoic acid.
Aufarbeitung
- temperaturethe resulting mixture was cooled to 0° C
- customSolid residues were removed by filtration
- extractionextracted twice with ether
- washrinsed once with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated in vacuo
- washThe concentrate was washed with carbon tetrachloride
- customrecrystallized from water
Quellen und Nachweise
- ORD-Eintrag
- ord-f701d6c925d54f6ebdab1a0f8bf6eb6a
- Quelldatensatz
- uspto-grants-2008_04
- Patentnummer
- US07358373B2
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