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Methylhydrazine → HCID 178481857, Verbindung

HRID 2387146
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2387146
[F:1][CH:2]([F:10])[C:3](=O)[CH2:4][C:5](OC)=[O:6].[CH3:11][NH:12][NH2:13]>CO>[F:1][CH:2]([F:10])[C:3]1[CH:4]=[C:5]([OH:6])[N:12]([CH3:11])[N:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 6061MethylhydrazineHCID 13179258Methyl 4,4-difluoro-3-oxobutanoate

Produkt 1

HCID 178481857HCID 178481857, VerbindungAusbeute 49,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of methyl 4,4-difluoro-3-oxobutanoate (64 g, 0.38 mol) in methanol (500 mL) was added methylhydrazine (20.5 mL, 0.38 mol). The reaction mixture was left to stir overnight at room temperature. The volatiles were removed in vacuo, toluene was added (400 mL), the mixture was evaporated again, and this procedure was repeated. The resulting solid residue was purified chromatographically on silica gel using ethyl acetate/dichloromethane mixture (1:2, Rf=0.35). The resulting oil was crystallized from ether (200 mL) and dried under the vacuum of a membrane pump (10 mm Hg) for 3 h to give 28 g (49.8%) of the title product.

Aufarbeitung

  1. waitThe reaction mixture was left
  2. customThe volatiles were removed in vacuo, toluene
  3. additionwas added (400 mL)
  4. customthe mixture was evaporated again
  5. customThe resulting solid residue was purified chromatographically on silica gel
  6. customThe resulting oil was crystallized from ether (200 mL)
  7. customdried under the vacuum of a membrane pump (10 mm Hg) for 3 h

Quellen und Nachweise

ORD-Eintrag
ord-375f6727a633438695d9c08f5128658b
Quelldatensatz
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08268835B2

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