Reaktionsgleichung
[CH:1]([CH:4]([C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1)[C:5](O)=[O:6])([CH3:3])[CH3:2].S(Cl)([Cl:17])=O>>[CH:1]([CH:4]([C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1)[C:5]([Cl:17])=[O:6])([CH3:3])[CH3:2]Komponenten
3
Versuchsvorschrift
10 g of the product of Step D were added to a mixture of 50 ml of petroleum ether (b.p.=35°-70° C.) and 20 ml of thionyl chloride and the mixture was refluxed for 4 hours and was then cooled. The mixture was evaporated to dryness to obtain 10.8 g of D 2-isopropyl-2-p-chlorophenyl acetyl chloride.
Aufarbeitung
- temperaturethe mixture was refluxed for 4 hours
- temperaturewas then cooled
- customThe mixture was evaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-55d226453b9140adbbf9185143dcf950
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04344895
Verknüpfte Notizen
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