Dimethyl Sulfate → Methyl 3-methoxy-2-(alpha,alpha,alpha-trifluoro-m-tolyl)-acrylate

HRID 648560Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 648560
[OH:1][CH:2]=[C:3]([C:8]1[CH:9]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:11]=[CH:12][CH:13]=1)[C:4]([O:6][CH3:7])=[O:5].S(OC)(O[CH3:22])(=O)=O>[OH-].[Na+].O>[CH3:22][O:1][CH:2]=[C:3]([C:8]1[CH:9]=[C:10]([C:14]([F:15])([F:16])[F:17])[CH:11]=[CH:12][CH:13]=1)[C:4]([O:6][CH3:7])=[O:5]

Komponenten

5

Edukt 2

HCID 6497Dimethyl Sulfate2×HCID 67828062Methyl 3-hydroxy-2-(alpha,alpha,alpha-trifluoro-m-tolyl)acrylate

Produkt 1

HCID 53807060Methyl 3-methoxy-2-(alpha,alpha,alpha-trifluoro-m-tolyl)-acrylate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 14798Sodium HydroxideLösungsmittel2×

Versuchsvorschrift

(ba) 26 g of methyl 3-hydroxy-2-(α,α,α-trifluoro-m-tolyl)acrylate were dissolved in 1N sodium hydroxide solution while cooling in an ice-bath and treated with 10.6 ml of dimethyl sulfate. The mixture was stirred at about 0° for about 40 hours and an additional 40 ml of 1N sodium hydroxide solution and 3.8 ml of dimethyl sulfate were added. After the reaction was completed, the mixture was diluted with water and extracted with methylene chloride. After drying with sodium sulfate, the extract was distilled, whereby methyl 3-methoxy-2-(α,α,α-trifluoro-m-tolyl)-acrylate was obtained as a colorless oil of b.p. 75°-90°/0.2 mm.

Aufarbeitung

  1. temperaturewhile cooling in an ice-bath
  2. extractionextracted with methylene chloride
  3. dry with materialAfter drying with sodium sulfate
  4. distillationthe extract was distilled

Quellen und Nachweise

ORD-Eintrag
ord-adada935c86147f0b440dcc8278ebe80
Quelldatensatz
uspto-grants-1988_04
Patentnummer
US04735940

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