Hydrochloric Acid → 2-Methylthio-2,2,2',4'-tetrafluoroacetophenone

HRID 1976924

Reaktionsgleichung

Reaktionsgleichung von HRID 1976924
CCCCCC.C([Li])CCC.Br[C:13]1[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=1[F:20].[F:21][C:22]([F:30])([S:28][CH3:29])[C:23](OCC)=[O:24].Cl>CCOCC>[F:20][C:14]1[CH:15]=[C:16]([F:19])[CH:17]=[CH:18][C:13]=1[C:23](=[O:24])[C:22]([F:30])([F:21])[S:28][CH3:29]

Komponenten

7

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A hexane solution (13.7 ml, 21.6 mmol) of 1.58 M n-butyllithium was added dropwise to a solution of 1-bromo-2,4-difluorobenzene (4.2 g, 21.8 mmol) in absolute ether (60 ml) at −70° C., and the mixture was stirred for 15 minutes at the same temperature. A solution of ethyl 2,2-difluoro-2-(methylthio)acetate (3.7 g, 21.6 mmol) in absolute ether (20 ml) was added to this solution at −70° C. After the resultant mixture was stirred for 1 hour at the same temperature, the temperature of the reaction mixture was raised to 0° C. for 1 hour. The reaction mixture was poured into diluted hydrochloric acid-containing ice to conduct extraction with ether. After the resultant ether solution was washed with water and dried, the solvent was distilled off. The resultant residue was purified by distillation under reduced pressure to obtain 1-(2,4-difluorophenyl)-2,2-difluoro-2-(methylthio)-1-ethanone (4.1 g, yield: 90.0%) as a colorless oil.

Aufarbeitung

  1. additioncontaining ice
  2. extractionextraction with ether
  3. washAfter the resultant ether solution was washed with water
  4. customdried
  5. distillationthe solvent was distilled off
  6. distillationThe resultant residue was purified by distillation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-05a8462147184f9aa1bf386379b403c3
Quelldatensatz
uspto-grants-2001_05
Patentnummer
US06229049B1

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