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Water → (1S,3S)-2,2-dimethyl-3-phenylcyclopropane-1-carboxylic acid

HRID 2240847
ノート
印刷プレビュー

反応式

HRID 2240847 の反応式
[CH3:1][C:2]1([CH3:13])[CH:4]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:3]1[C:11]#N.[OH-:14].[K+].[OH2:16]>C(O)CO.[Cl-].[Na+].O>[CH3:1][C:2]1([CH3:13])[C@@H:4]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)[C@@H:3]1[C:11]([OH:16])=[O:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 14797Potassium HydroxideHCID 134298982,2-Dimethyl-3-phenylcyclopropanecarbonitrile

生成物 1

HCID 68582304(1S,3S)-2,2-dimethyl-3-phenylcyclopropane-1-carboxylic acid収率 95%

試薬・触媒・溶媒 2

HCID 174Ethylene Glycol溶媒HCID 57417360
Sodium chloride; water
溶媒

反応条件

温度
165 °C

実験手順

A mixture of 2,2-dimethyl-3-phenyl-cyclopropanecarbonitrile (cis/trans mixture, 3.2 g, 18.7 mmol) and freshly ground KOH (3.143 g, 56.1 mmol) in ethylene glycol was heated at 165° C. for 28 hours. The reaction mixture was then cooled and poured into a mixture of water and brine (300 mL). The resulting mixture was extracted 3 times with ethyl ether, the combined organic extracts were dried over Na2SO4, filtered and evaporated under reduced pressure to give 3.36 g (95% yield) of trans-2,2-dimethyl-3-phenyl-cyclopropanecarboxylic acid.

後処理

  1. temperatureThe reaction mixture was then cooled
  2. extractionThe resulting mixture was extracted 3 times with ethyl ether
  3. dry with materialthe combined organic extracts were dried over Na2SO4
  4. filtrationfiltered
  5. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-26bc0c78278f40cc8951ed3d0ab7b1a9
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723391B2

反応ノート

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