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Carbon tetrabromide → 4-(2,2-Dibromovinyl)cyclohexanone

HRID 653362
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HRID 653362 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:20]([Br:24])(Br)(Br)[Br:21].[CH:25]([CH:27]1[CH2:32][CH2:31][C:30](=[O:33])[CH2:29][CH2:28]1)=O>C(Cl)Cl>[Br:21][C:20]([Br:24])=[CH:25][CH:27]1[CH2:32][CH2:31][C:30](=[O:33])[CH2:29][CH2:28]1
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참가 물질

5

반응물 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 111709734-Oxocyclohexane-1-carbaldehyde

생성물 1

HCID 197393224-(2,2-Dibromovinyl)cyclohexanone수율 85.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 36.72 g of triphenylphosphine in 200 ml of methylene chloride was treated slowly at -20° C. with 23.22 g of carbon tetrabromide and stirred for a further 10 minutes. Subsequently, the mixture was added dropwise by means of a cannula to a solution, cooled to -60° C., of 6.30 g of 4-formylcyclohexanone in 100 ml of methylene chloride. The mixture was stirred at -60° C. for a further 15 minutes and then partitioned in water/methylene chloride. The aqueous phases were extracted a further twice with methylene chloride. The organic phases were washed twice with water, dried over magnesium sulphate and evaporated. Low-pressure chromatography of the resulting, pale yellow oil (16 g) on silica gel with ethyl acetate/petroleum ether (vol. 10:90) gave 12.08 g (85.8%) of 4-(2,2-dibromovinyl)cyclohexanone as a pale yellow liquid.

후처리

  1. additionSubsequently, the mixture was added dropwise by means of a cannula to a solution
  2. stirringThe mixture was stirred at -60° C. for a further 15 minutes
  3. custompartitioned in water/methylene chloride
  4. extractionThe aqueous phases were extracted a further twice with methylene chloride
  5. washThe organic phases were washed twice with water
  6. dry with materialdried over magnesium sulphate
  7. customevaporated

출처 및 근거

ORD 기록
ord-5ef9db48bb2b4b15bbfecc19da04d668
출처 데이터셋
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04676604

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