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

HRID 1063477
ノート
印刷プレビュー

反応式

HRID 1063477 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-486fa88912014a20b3534d7a866b4f23
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06965029B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート