Reaktionsgleichung
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1.[Br:12]Br.O>C(=S)=S>[F:1][C:2]([F:10])([F:11])[C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][C:8]=1[Br:12]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3-Trifluoromethylphenol (compound I) (5.0 g) was dissolved in carbon disulfide (3.0 ml) and then to the solution was added a solution of bromine (5.0 g) in carbon disulfide (2.0 ml) over a period of about 15 minutes at 25° C. or less, followed by allowing the reaction to proceed for 2 hours at 25° C. The resulting reaction mixture was added to water (10 ml) and then subjected to repeated extraction with methylene chloride. The methylene chloride layer was washed with aqueous sodium hydrogen-carbonate solution and then with water and dehydration-dried by adding anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to obtain 3-trifluoromethyl-4-bromophenol (compound II, 4.4 g).
Aufarbeitung
- customthe reaction
- customThe resulting reaction mixture
- extractionextraction with methylene chloride
- washThe methylene chloride layer was washed with aqueous sodium hydrogen-carbonate solution
- dry with materialwith water and dehydration-dried
- additionby adding anhydrous sodium sulfate
- customThe solvent was removed by distillation under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-f290902f7b8f414595c1f7c01ec506ef
- Quelldatensatz
- uspto-grants-1993_02
- Patentnummer
- US05183934
Verknüpfte Notizen
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