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Ethanol → Ethyl 2-bromo-4-(trifluoromethyl)benzoate

HRID 439548
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반응식

HRID 439548 반응식
[Br:1][C:2]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(=O)(=O)(O)O.[CH2:20](O)[CH3:21]>>[Br:1][C:2]1[CH:10]=[C:9]([C:11]([F:12])([F:13])[F:14])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH2:20][CH3:21])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 676052-Bromo-4-(trifluoromethyl)benzoic acid

생성물 1

HCID 15766264Ethyl 2-bromo-4-(trifluoromethyl)benzoate수율 100%

실험 절차

238 g (0.885 mol) of 2-bromo-4-(trifluoromethyl)benzoic acid, 1000 ml of absolute ethanol and 100 ml of concentrated sulfuric acid are introduced successively into a 2-liter round-bottomed flask. The reaction mixture is brought to reflux for 6 hours and then poured, after cooling, onto 2.5 liters of ice-cold water; the oil formed is extracted with ethyl acetate. The organic phase is successively washed with water, with 1N sodium hydroxide solution and then again with water. After drying over magnesium sulfate, the solvent is evaporated to provide 263 g (yield: 100%) of ethyl 2-bromo-4-(trifluoromethyl)benzoate in the form of a yellow oil.

후처리

  1. temperatureto reflux for 6 hours
  2. additionpoured
  3. customthe oil formed
  4. extractionis extracted with ethyl acetate
  5. washThe organic phase is successively washed with water, with 1N sodium hydroxide solution
  6. dry with materialAfter drying over magnesium sulfate
  7. customthe solvent is evaporated

출처 및 근거

ORD 기록
ord-bb6e42ca444748fd9e19e6039f031dd1
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05514719

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