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Potassium Hydroxide → (1R,2S)-2-methoxycarbonylcyclopropane-1-carboxylic acid

HRID 498114
ノート
印刷プレビュー

反応式

HRID 498114 の反応式
[C@@H:1]1([C:8]([O:10]C)=[O:9])[CH2:3][C@@H:2]1[C:4]([O:6][CH3:7])=[O:5].[OH-].[K+]>CO>[CH3:7][O:6][C:4]([C@H:2]1[CH2:3][C@H:1]1[C:8]([OH:10])=[O:9])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 642979Dimethyl (1R,2S)-cyclopropane-1,2-dicarboxylate

生成物 1

HCID 12510973(1R,2S)-2-methoxycarbonylcyclopropane-1-carboxylic acid収率 92.6%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To 150 ml of a methanol solution of 14.68 g (92.8 mmol) of dimethyl cis-1,2-cyclopropanedicarboxylate was added 67 ml of an aqueous solution of 7.52 g (113.9 mmol) of potassium hydroxide under cooling with ice, and the mixture was stirred at room temperature for 24 hours. After completion of the reaction, the solvent was removed by evaporation under reduced pressure, and to the residue was added water. The reaction mixture was washed with diethyl ether. The aqueous layer was adjusted to pH 2 with concentrated hydrochloric acid and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give 12.38 g (92.5%) of the title compound as a colorless oily substance.

後処理

  1. temperatureunder cooling with ice
  2. customAfter completion of the reaction
  3. customthe solvent was removed by evaporation under reduced pressure
  4. additionto the residue was added water
  5. washThe reaction mixture was washed with diethyl ether
  6. extractionextracted with ethyl acetate
  7. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  8. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-f8ca7fa0ed9a412fae5f876e19778033
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06949662B2

反応ノート

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