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Hydrochloric Acid → Sodium 2-oxo-3-phenylbutanoate

HRID 1086339
ノート
印刷プレビュー

反応式

HRID 1086339 の反応式
[OH-].[Na+:2].[C:3]1([CH2:9][C:10](=[O:14])[C:11]([O-:13])=[O:12])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[Na+].[CH3:16]I.Cl>CO>[O:14]=[C:10]([CH:9]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)[CH3:16])[C:11]([O-:13])=[O:12].[Na+:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 14798Sodium Hydroxide2 回HCID 23667645Sodium phenylpyruvate

生成物 1

HCID 23676252Sodium 2-oxo-3-phenylbutanoate

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A 2N aqueous solution of sodium hydroxide (10 ml, 20 mmoles) and 30 ml of methanol were added to 3.92 g (20 mmoles) of sodium phenylpyruvate to form a solution. Then, 1.25 ml of methyl iodide was added, and the mixture was stirred at room temperature for 24 hours. The reaction mixture was acidified with 1N hydrochloric acid, and extracted with 150 ml of ether. The ether layer was dried over magnesium sulfate, and concentrated under reduced pressure to give a pale yellowish white oil. A 3N aqueous solution of sodium hydroxide (6.5 ml) was added, and the mixture was concentrated. Ether was added to the resulting semi-solid mixture, and the precipitated sodium 2-oxo-3-phenylbutanoate was isolated by filtration as a white solid (1.62 g, yield 85 %).

後処理

  1. customto form a solution
  2. extractionextracted with 150 ml of ether
  3. dry with materialThe ether layer was dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customto give a pale yellowish white oil
  6. concentrationthe mixture was concentrated
  7. additionEther was added to the resulting semi-solid mixture

出典と根拠

ORDレコード
ord-9088c69b4e8d4176a43a3a75d6754416
出典データセット
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05028738

反応ノート

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