Reaktionsgleichung
O.[O:2]=[CH:3][C:4]([Cl:7])([Cl:6])[Cl:5].[CH2:8]([OH:13])[CH2:9][CH2:10][CH2:11][CH3:12]>C1C=CC=CC=1>[CH2:8]([O:2][CH:3]([O:13][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[C:4]([Cl:7])([Cl:6])[Cl:5])[CH2:9][CH2:10][CH2:11][CH3:12]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 5 g of chloral-hydrate, 10 ml of amyl-alcohol, 0.1 g of 4-methyl-sulphonic acid and 50 ml of benzene is kept at reflux temperature and the formed water is separated by means of a Dean-Stark apparatus. After a reaction time of 9 hours the benzene is washed with a sodium hydrogen carbonate solution and water, dried on magnesium sulfate, then it is vacuum-distilled.
Aufarbeitung
- temperatureat reflux temperature
- customthe formed water is separated by means of a Dean-Stark apparatus
- washAfter a reaction time of 9 hours the benzene is washed with a sodium hydrogen carbonate solution and water
- customdried on magnesium sulfate
- distillationit is vacuum-distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-c1dab98a054a4eb980152bafb5a7767f
- Quelldatensatz
- uspto-grants-1992_05
- Patentnummer
- US05116402
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