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Water → 7,8-Epoxy-6-oxo-octanoic acid methyl ester

HRID 1063477
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HRID 1063477 반응식
C([O-])([O-])=[O:2].C([O-])([O-])=O.OO.OO.OO.[Na+].[Na+].[Na+].[Na+].[CH3:19][O:20][C:21](=[O:30])[CH2:22][CH2:23][CH2:24][CH2:25][C:26](=[O:29])[CH:27]=[CH2:28].O>CO>[CH3:19][O:20][C:21](=[O:30])[CH2:22][CH2:23][CH2:24][CH2:25][C:26](=[O:29])[CH:27]1[O:2][CH2:28]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 159762Sodium percarbonateHCID 179590916-Oxo-7-octenoic acid methyl ester

생성물 1

HCID 179590927,8-Epoxy-6-oxo-octanoic acid methyl ester수율 88.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

39.1 g (250 mmol) of sodium percarbonate were added in four portions at room temperature, over a period of 2 hours, with stirring, to 13.9 g (82 mmol) of 6-oxo-7-octenoic acid methyl ester in 210 ml of methanol. After stirring for a further one hour at room temperature, the reaction mixture was added to 1000 ml of water and extracted several times with methylene chloride. The combined organic phases were washed with water. After drying over sodium sulfate, the solvent was distilled off using a rotary evaporator. 13.5 g (88%) of 7,8-epoxy-6-oxo-octanoic acid methyl ester were obtained.

후처리

  1. extractionextracted several times with methylene chloride
  2. washThe combined organic phases were washed with water
  3. dry with materialAfter drying over sodium sulfate
  4. distillationthe solvent was distilled off
  5. customa rotary evaporator

출처 및 근거

ORD 기록
ord-486fa88912014a20b3534d7a866b4f23
출처 데이터셋
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06965029B2

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