Reaktionsgleichung
[CH3:1][C:2]1([CH3:22])[CH2:6][O:5][C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[C:13]2[CH:18]=[CH:17][C:16]([C:19]([OH:21])=[O:20])=[CH:15][CH:14]=2)=[N:3]1.S(Cl)(Cl)=O.[CH2:27](Cl)Cl>>[CH3:1][C:2]1([CH3:22])[CH2:6][O:5][C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[C:13]2[CH:18]=[CH:17][C:16]([C:19]([O:21][CH3:27])=[O:20])=[CH:15][CH:14]=2)=[N:3]1Komponenten
Versuchsvorschrift
10.0 g (33.8 mmol) of 4,4-dimethyl-2-(4'-carboxybiphenyl-2-yl)oxazoline was dissolved in methylene chloride (200 ml). 4.8 g (40.3 mmol) of thionyl chloride was added thereto, followed by stirring at room temperature for 2 hours. The reaction liquid was subjected to vacuum concentration. Methanol (100 ml) was added to the residue, followed by stirring for 3 hours. After distilling out the solvent under a reduced pressure, methylene chloride and a saturated aqueous solution of sodium hydrogencarbonate were added to the residue and obtained mixture was caused liquid-liquid separation. After washing with water and drying, vacuum concentration was conducted. The residue was purified by silica gel column chromatography (an ethyl acetate/n-hexane system) to give 9.53 g of the title compound as an oil (yield 91%).
Aufarbeitung
- customThe reaction liquid
- concentrationwas subjected to vacuum concentration
- additionMethanol (100 ml) was added to the residue
- stirringby stirring for 3 hours
- distillationAfter distilling out the solvent under a reduced pressure, methylene chloride
- additiona saturated aqueous solution of sodium hydrogencarbonate were added to the residue
- customobtained mixture
- customliquid-liquid separation
- washAfter washing with water
- customdrying
- concentrationvacuum concentration
- customThe residue was purified by silica gel column chromatography (an ethyl acetate/n-hexane system)
Quellen und Nachweise
- ORD-Eintrag
- ord-be8a3c1f1c4644fbbc34e47b1141fb04
- Quelldatensatz
- uspto-grants-1996_09
- Patentnummer
- US05554757
Verknüpfte Notizen
Wird geladen…