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Hydrochloric Acid → Sodium 2-oxo-3-phenylbutanoate

HRID 1086338
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HRID 1086338 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 997Phenylpyruvic acidHCID 6328Methyl iodideHCID 14798Sodium Hydroxide2회

생성물 1

HCID 23676252Sodium 2-oxo-3-phenylbutanoate수율 81%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f9e10aa7834042ca9059a2dcd6aabd3a
출처 데이터셋
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05028738

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