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Phenylpyruvic acid → Sodium 2-oxo-3-phenylbutanoate

HRID 1086340
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HRID 1086340 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>O1CCCC1>[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

5

반응물 3

HCID 997Phenylpyruvic acidHCID 6328Methyl iodideHCID 14798Sodium Hydroxide

생성물 1

HCID 23676252Sodium 2-oxo-3-phenylbutanoate수율 68%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A 1N aqueous solution of sodium hydroxide (20 ml, 20 mmoles) and 30 ml of tetrahydrofuran 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 concentrated, and ether was added to the resulting pale yellowish white semi-solid. The precipitated sodium 2-oxo-3-phenylbutanoate as a white solid (0.68 g, yield 68 %) was isolated by filtration.

후처리

  1. customto form a solution
  2. concentrationThe reaction mixture was concentrated
  3. additionether was added to the resulting pale yellowish white semi-solid

출처 및 근거

ORD 기록
ord-e00b7c8585e447fbb58d58e56489a553
출처 데이터셋
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05028738

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