Methyl p-toluenesulfonate → 3-Methoxy-4,4,4-trifluoro-2-butenoic acid ethyl ester

HRID 366300

Reaktionsgleichung

Reaktionsgleichung von HRID 366300
[C:1](=O)([O-])[O-].[Cs+].[Cs+].[F:7][C:8]([F:18])([F:17])[C:9](=[O:16])[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12].S(C1C=CC(C)=CC=1)(OC)(=O)=O>CN(C)C=O>[CH3:1][O:16][C:9]([C:8]([F:17])([F:18])[F:7])=[CH:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]

Komponenten

5

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

Cesium carbonate (132.8 g) was added to a mixture of ethyl 4,4,4-trifluoroacetoacetate (75.0 g) and dimethylformamide (400 ml). The reaction mixture was heated to 20° C. for 30 minutes. A mixture of methyl tosylate (83.4 g) and dimethylformamide (150 ml) was added to the resulting reaction mixture within 40 minutes. The mixture was heated for 3 hours and cooled to room temperature. Upon dilution with water (800 ml) the reaction mixture was extracted with diethyl ether three times. The combined organic phases were washed with water and dried. The mixture was concentrated and the residue distilled under reduced pressure to yield the product as a clear liquid (48.5 g, 60 %) with a boiling point of 62-70° C. at 12 mm.

Aufarbeitung

  1. additionwas added to the resulting reaction mixture within 40 minutes
  2. temperatureThe mixture was heated for 3 hours
  3. temperaturecooled to room temperature
  4. extractionUpon dilution with water (800 ml) the reaction mixture was extracted with diethyl ether three times
  5. washThe combined organic phases were washed with water
  6. customdried
  7. concentrationThe mixture was concentrated
  8. distillationthe residue distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-dd6e47b8277241ac9ff8f5d988721dab
Quelldatensatz
uspto-grants-2000_10
Patentnummer
US06130188

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