Potassium bisulfate → 1-(4,5-Diphenyloxazol-2-yl)-5-(3-methoxybenzyl)cyclopentene
Reaktionsgleichung
O[C:2]1([C:16]2[O:17][C:18]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)=[C:19]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[N:20]=2)[CH2:6][CH2:5][CH2:4][CH:3]1[CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14][CH3:15])[CH:9]=1.S([O-])(O)(=O)=O.[K+]>C1(C)C=CC=CC=1>[C:21]1([C:19]2[N:20]=[C:16]([C:2]3[CH:3]([CH2:7][C:8]4[CH:13]=[CH:12][CH:11]=[C:10]([O:14][CH3:15])[CH:9]=4)[CH2:4][CH2:5][CH:6]=3)[O:17][C:18]=2[C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 1-hydroxy-1-(4,5-diphenyloxazol-2-yl)-2-(3-methoxybenzyl)cyclopentane (8.0 g) in toluene (160 ml) was added potassium hydrogensulfate (2.6 g), and the solution was stirred for 1 hour under reflux. After being cooled, the solution was washed with water, saturated sodium bicarbonate aqueous solution and brine and evaporated in vacuo. The oily residue was chromatographed on silica gel to afford a mixture (8.0 g) of 1-(4,5-diphenyloxazol-2-yl)-5-(3-methoxybenzyl)-cyclopentene and 1-(4,5-diphenyloxazol-2-yl)-2-(3-methoxybenzyl)cyclopentene.
Aufarbeitung
- temperatureunder reflux
- temperatureAfter being cooled
- washthe solution was washed with water, saturated sodium bicarbonate aqueous solution and brine
- customevaporated in vacuo
- customThe oily residue was chromatographed on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-191f60b0ae0943ce9325336ff7c37d9d
- Quelldatensatz
- uspto-grants-2000_02
- Patentnummer
- US06025375
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