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

HRID 2367864
ノート
印刷プレビュー

反応式

HRID 2367864 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 1382182,2,5,5-Tetramethyl-3,4-hexanedione収率 82.2%

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-cf1e82c912544c77948ee3700f6d3928
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08703103B2

反応ノート

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