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

HRID 1733430
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반응식

HRID 1733430 반응식
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]
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참가 물질

3

반응물 2

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

생성물 1

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

반응 조건

온도
80 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-1a9b9497231d4624b18dec1c85193d0e
출처 데이터셋
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04242278

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