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1,1-Dibromoethane → 1-(2-bromoethoxy)-2-chloro-4-nitrobenzene

HRID 1106864
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HRID 1106864 반응식
[Br:1][CH:2](Br)[CH3:3].[Cl:5][C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[CH:9]=[CH:8][C:7]=1[OH:15]>C(=O)([O-])[O-].[K+].[K+].O>[Cl:5][C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[CH:9]=[CH:8][C:7]=1[O:15][CH2:3][CH2:2][Br:1]
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참가 물질

5

반응물 2

HCID 112011,1-DibromoethaneHCID 12074Nitrofungin

생성물 1

HCID 3099731-(2-bromoethoxy)-2-chloro-4-nitrobenzene수율 86.6%

시약·촉매·용매 2

HCID 962Water용매HCID 11430Potassium Carbonate용매

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온도
85 °C

실험 절차

Dibromoethane (14.9 ml, 0.1728 mol) and 2-chloro-4-nitrophenol (10 g, 0.0576 mol) were dissolved in dimethylfomamide (250 ml) and potassium carbonate (9.55 g) was added to the resulting solution, followed by stirring at 85° C. for 30 min. Thereafter, the reaction solution was diluted with water and subjected to three extractions with ethyl acetate. The organic extracts were combined, dried with magnesium and the solvent was evaporated; thereafter, the residue was purified by being subjected to column chromatography using a 1:1 solvent system of n-hexane and ethyl acetate as an eluent and the fractions containing the end product were collected and subjected to evaporation to yield the end compound 1-(2-chloro-4-nitrophenoxy)-2-bromoethane (14.0 g) as a yellow solid mass.

후처리

  1. additionwas added to the resulting solution
  2. extractionsubjected to three extractions with ethyl acetate
  3. dry with materialdried with magnesium
  4. customthe solvent was evaporated
  5. customthereafter, the residue was purified
  6. additionthe fractions containing the end product
  7. customwere collected
  8. customsubjected to evaporation

출처 및 근거

ORD 기록
ord-e0c3fcc476fb47c5a5986c65e1824f45
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06057358

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