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Sodium Hydroxide → 2,2,5,5-Tetramethyl-3,4-hexanedione

HRID 2367864
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2367864
[CH3:1][C:2]([CH3:12])([C:4](=[O:11])[CH:5]([OH:10])[C:6]([CH3:9])([CH3:8])[CH3:7])[CH3:3].[Mn]([O-])(=O)(=O)=O.[K+].[OH-].[Na+]>CCCCCC>[CH3:8][C:6]([CH3:9])([C:5](=[O:10])[C:4](=[O:11])[C:2]([CH3:12])([CH3:3])[CH3:1])[CH3:7]
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Komponenten

5

Edukt 3

HCID 14798Sodium HydroxideHCID 2195934-Hydroxy-2,2,5,5-tetramethylhexan-3-oneHCID 516875Potassium Permanganate

Produkt 1

HCID 1382182,2,5,5-Tetramethyl-3,4-hexanedioneAusbeute 82,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8058HexaneLösungsmittel

Versuchsvorschrift

7.8 g (0.045 moles) of 2,2,5,5-tetramethyl-4-hydroxy-3-hexanone were dissolved in 90 ml of hexane and stirred vigorously with 157 ml of 1M aqueous potassium permanganate solution containing 1.8 g (0.045 moles) of sodium hydroxide. This mixture was then refluxed overnight. The mixture was then cooled to room temperature and the hexane layer separated. The aqueous layer was then extracted three times with 50 ml of hexane. The hexane solutions were then combined and washed three times with 50 ml of pure water before drying over anhydrous magnesium sulfate. The mixture was then filtered and the hexane distilled off at atmospheric pressure to yield 6.3 g of 2,2,5,5-tetramethyl-3,4-hexanedione (82% of theoretical).

Aufarbeitung

  1. temperatureThis mixture was then refluxed overnight
  2. customthe hexane layer separated
  3. extractionThe aqueous layer was then extracted three times with 50 ml of hexane
  4. washwashed three times with 50 ml of pure water
  5. dry with materialbefore drying over anhydrous magnesium sulfate
  6. filtrationThe mixture was then filtered
  7. distillationthe hexane distilled off at atmospheric pressure

Quellen und Nachweise

ORD-Eintrag
ord-cf1e82c912544c77948ee3700f6d3928
Quelldatensatz
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08703103B2

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