Reaktionsgleichung
[I:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[OH-].[Na+].C1COCC1.Cl[CH:17]([F:19])[F:18]>O>[F:18][CH:17]([F:19])[O:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
100 g (0.455 mol) of 4-iodophenol and 54.6 g (1.365 mol) of sodium hydroxide are added to a mixture of 300 ml of THF and 30 ml of water. After stirring for about 1/2 hour, the mixture is evaporated in a rotary evaporator; this is repeated after the addition of 200 ml of toluene. The residue is taken up in 400 ml of THF. The mixture is cooled to 0° C., 47.1 g (0.545 mol) of chlorodifluoromethane are introduced, and the mixture is then stirred for 1 hour. It is then stirred at about +5° C. for 18 hours. The solution above the resulting slurry-like precipitate was decanted off. It was evaporated in a rotary evaporator, and the residue was chromatographed through a silica gel column, using petroleum ether as eluent.
Aufarbeitung
- customthe mixture is evaporated in a rotary evaporator
- additionafter the addition of 200 ml of toluene
- stirringthe mixture is then stirred for 1 hour
- stirringIt is then stirred at about +5° C. for 18 hours
- customThe solution above the resulting slurry-like precipitate was decanted off
- customIt was evaporated in a rotary evaporator
- customthe residue was chromatographed through a silica gel column
Quellen und Nachweise
- ORD-Eintrag
- ord-a749331d7eec4c6295277b8e570169b7
- Quelldatensatz
- uspto-grants-1995_02
- Patentnummer
- US05389292
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