Ethylene Glycol → HCID 22394927, Verbindung
Reaktionsgleichung
[CH3:1][CH:2]1[CH2:7][CH2:6][C:5](=[O:8])[CH2:4][CH:3]1[S:9]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)(=[O:11])=[O:10].[CH2:18](O)[CH2:19][OH:20].C(=O)(O)[O-].[Na+]>C1C=CC=CC=1>[CH2:18]1[CH2:19][O:20][C:5]2([CH2:6][CH2:7][CH:2]([CH3:1])[CH:3]([S:9]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)(=[O:10])=[O:11])[CH2:4]2)[O:8]1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 2.45 g of 4-methyl-3-(phenylsulfonyl)-cyclohexan-1-one in 40 ml of benzene, were added 0.7 ml of 1,2-ethanediol and 0.2 g of anhydrous paratoluenesulfonic acid. The resulting mixture was heated under reflux for 4 hours. After the reaction, a 2M aqueous sodium bicarbonate solution was added and the resulting mixture was extracted with ethyl acetate three times. The combined organic layers were washed with saturated saline, and dried over magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was recrystallized from ethyl ether, whereby 1,1-(ethylenedioxy)-4-methyl-3-(phenylsulfonyl)-cyclohexane was obtained in the form of white crystals. Yield: 97%, Melting point: 105 to 106° C.
Aufarbeitung
- temperatureThe resulting mixture was heated
- temperatureunder reflux for 4 hours
- customAfter the reaction
- extractionthe resulting mixture was extracted with ethyl acetate three times
- washThe combined organic layers were washed with saturated saline
- dry with materialdried over magnesium sulfate
- distillationThe solvent was then distilled off under reduced pressure
- customThe residue was recrystallized from ethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-cc9633e2e1ac41dc8a7fa14151867efc
- Quelldatensatz
- uspto-grants-2007_01
- Patentnummer
- US07166642B1
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