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Sodium Hydroxide → 3-(2,2-Dibromovinyl)-2,2-dimethylcyclopropane-1-carboxylic acid

HRID 2059157
ノート
印刷プレビュー

反応式

HRID 2059157 の反応式
Br[C:2]([Br:13])([Br:12])[CH2:3][CH:4]1[C:7]([CH3:9])([CH3:8])[CH:6](Cl)[C:5]1=[O:11].[OH-:14].[Na+]>>[Br:13][C:2]([Br:12])=[CH:3][CH:4]1[C:7]([CH3:8])([CH3:9])[CH:6]1[C:5]([OH:11])=[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

3

反応物 2

HCID 14798Sodium HydroxideHCID 125872302-Chloro-3,3-dimethyl-4-(2,2,2-tribromoethyl)cyclobutan-1-one

生成物 1

HCID 1812483-(2,2-Dibromovinyl)-2,2-dimethylcyclopropane-1-carboxylic acid収率 100%

反応条件

温度
80 °C

実験手順

A mixture of 800 mg (0.02 mole) of 2-(2',2',2'-tribromoethyl)-3,3-dimethyl-4-chlorocyclobutan-1-one and 5.6 ml of 5% by weight of aqueous sodium hydroxide solution is stirred for 18 hours at 0° C. and subsequently for one additional hour at 80° C. Then the reaction mixture is cooled to room temperature washed with diethyl ether, acidified with concentrated hydrochloric acid and extracted with diethyl ether. The extract is washed with water and dried over magnesium sulphate. After evaporation of the diethyl ether there is obtained 0.59 g (100% of theoriy) of 2-(2',2'-dibromovinyl)-3,3-dimethylcyclopropane-1-carboxylic acid consisting to 80% of the cis-isomer and to 20% of the trans-isomer.

後処理

  1. temperatureThen the reaction mixture is cooled to room temperature
  2. washwashed with diethyl ether
  3. extractionextracted with diethyl ether
  4. washThe extract is washed with water
  5. dry with materialdried over magnesium sulphate
  6. customAfter evaporation of the diethyl ether

出典と根拠

ORDレコード
ord-3bab2ea77fd34a62b37e6b6c75198634
出典データセット
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04322374

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート