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Hydrochloric Acid → Sodium 2-oxo-3-phenylbutanoate

HRID 1086338
ノート
印刷プレビュー

反応式

HRID 1086338 の反応式
[OH-].[Na+:2].[C:3]1([CH2:9][C:10](=[O:14])[C:11]([OH:13])=[O:12])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH3:15]I.Cl>CO>[O:14]=[C:10]([CH:9]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)[CH3:15])[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 997Phenylpyruvic acidHCID 6328Methyl iodideHCID 14798Sodium Hydroxide2 回

生成物 1

HCID 23676252Sodium 2-oxo-3-phenylbutanoate収率 81%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A 1N aqueous solution of sodium hydroxide (20 ml, 20 mmoles) and 40 ml of methanol were added to 1.64 g (10.0 mmoles) of phenylpyruvic acid to form a solution. Then, 2.0 ml of methyl iodide was added, and the mixture was stirred at room temperature for 10 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 solid. To the solid was added 3 ml of a 3N aqueous solution of sodium hydroxide, and the mixture was concentrated under reduced pressure. Ether was added to the resulting semi-solid mixture, and the precipitated sodium 2-oxo-3-phenylbutanoate was isolated as a white solid (1.62 g; yield 81 %) by filtration.

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 solid
  6. concentrationthe mixture was concentrated under reduced pressure
  7. additionEther was added to the resulting semi-solid mixture

出典と根拠

ORDレコード
ord-f9e10aa7834042ca9059a2dcd6aabd3a
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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