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

HRID 1789629
ノート
印刷プレビュー

反応式

HRID 1789629 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6340IodoethaneHCID 6569Methyl Ethyl Ketone2 回HCID 73763-(Trifluoromethyl)phenolHCID 11430Potassium Carbonate

生成物 1

HCID 184153071-Ethoxy-3-(trifluoromethyl)benzene

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-e53b31a39b7e456887d2989addfbee81
出典データセット
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07070838B2

反応ノート

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