Sulfuric Acid → 2-(2,6-Difluorophenyl)acetohydrazide

HRID 2372401Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2372401
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[CH2:9][C:10]([OH:12])=O.S(=O)(=O)(O)O.O.[NH2:19][NH2:20]>C(O)C>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[CH2:9][C:10]([NH:19][NH2:20])=[O:12]

Komponenten

5

Versuchsvorschrift

70.4 g (0.41 mol) of 2,6-difluorophenylacetic acid, 700 ml of ethanol and 35 ml of concentrated sulphuric acid are heated under reflux for 3 hours. The reaction mixture is then concentrated by evaporation, taken up in dichloromethane and the solution is extracted by shaking in succession with water, 2N sodium carbonate solution and again with water. After drying over magnesium sulphate, the organic phase is concentrated by evaporation. The residue is dissolved in 560 ml of ethanol. After the addition of 30 ml (31 g; 0.62 mol) of hydrazine hydrate, the whole is heated under reflux for 4 days. After cooling, the resulting crystals are filtered off to yield 56.4 g (74% of the theoretical yield) of 2,6-difluorophenylacetic acid hydrazide which melts at 177-178°.

Aufarbeitung

  1. temperatureunder reflux for 3 hours
  2. concentrationThe reaction mixture is then concentrated by evaporation
  3. extractionthe solution is extracted
  4. dry with materialAfter drying over magnesium sulphate
  5. concentrationthe organic phase is concentrated by evaporation
  6. dissolutionThe residue is dissolved in 560 ml of ethanol
  7. temperaturethe whole is heated
  8. temperatureunder reflux for 4 days
  9. temperatureAfter cooling
  10. filtrationthe resulting crystals are filtered off
  11. customto yield 56.4 g (74% of the

Quellen und Nachweise

ORD-Eintrag
ord-82dfaa7e0fb545bfbe2df6f7431b8260
Quelldatensatz
uspto-grants-1992_03
Patentnummer
US05098922

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