Water → 2-Chloro-1-(2,4-difluorophenyl)-2-fluoroethan-1-one
Reaktionsgleichung
[F:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([F:11])=[CH:7][C:6]=1[F:12])=[O:4].O.S(Cl)([Cl:17])(=O)=O>>[F:1][CH:2]([Cl:17])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([F:11])=[CH:7][C:6]=1[F:12])=[O:4]Komponenten
4
Versuchsvorschrift
A solution of 2,2',4'-trifluoroacetophenone (1.60 g; 9.2 mM) in sulphuryl chloride (4 ml) was heated at 75° for 18 hours. The mixture was then cooled and iced-water (40 ml) was added. The product was extracted into ether (80 ml), which was washed with water and aqueous sodium bicarbonate solution, and then dried over magnesium sulphate. Evaporation yielded the desired product as a colourless, intensely lachrymatory liquid (2.0 g; 100%).
Aufarbeitung
- temperatureThe mixture was then cooled
- extractionThe product was extracted into ether (80 ml), which
- washwas washed with water and aqueous sodium bicarbonate solution
- dry with materialdried over magnesium sulphate
- customEvaporation
Quellen und Nachweise
- ORD-Eintrag
- ord-0dff33e52fe64197946070a2cd32454e
- Quelldatensatz
- uspto-grants-1990_10
- Patentnummer
- US04960782
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