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Iodoethane → 1-Ethoxy-3-(trifluoromethyl)benzene

HRID 1789629
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반응식

HRID 1789629 반응식
C(=O)([O-])[O-].[K+].[K+].[CH2:7](C(C)=O)[CH3:8].C(I)C.[F:15][C:16]([F:25])([F:24])[C:17]1[CH:18]=[C:19]([OH:23])[CH:20]=[CH:21][CH:22]=1>O>[CH2:7]([O:23][C:19]1[CH:18]=[C:17]([C:16]([F:24])([F:25])[F:15])[CH:22]=[CH:21][CH:20]=1)[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6340IodoethaneHCID 6569Methyl Ethyl Ketone2회HCID 73763-(Trifluoromethyl)phenolHCID 11430Potassium Carbonate

생성물 1

HCID 184153071-Ethoxy-3-(trifluoromethyl)benzene

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Potassium carbonate (22.6 g) and then a mixture of methyl ethyl ketone (MEK) (150 mL) and ethyl iodide (47.8 g) were added to a mixture of MEK (310 mL) and 3-trifluoromethylphenol (a) (25.0 g) at room temperature, and the reaction mixture was heated and stirred for 2 hours. After returning the mixture to room temperature, water was added for liquid separation and the aqueous layer was extracted three times with diethyl ether. The organic layers were combined, washed with an 1 M aqueous sodium hydroxide solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 19.3 g of Compound (b).

후처리

  1. temperaturethe reaction mixture was heated
  2. customto room temperature
  3. extractionthe aqueous layer was extracted three times with diethyl ether
  4. washwashed with an 1 M aqueous sodium hydroxide solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-e53b31a39b7e456887d2989addfbee81
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07070838B2

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