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Hydrogen Peroxide → 3-Fluoro-2-phenylsulfinyl-5-trifluoromethylpyridine

HRID 636067
ノート
印刷プレビュー

反応式

HRID 636067 の反応式
[F:1][C:2]1[C:3]([S:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[N:4][CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.FC(F)(F)C(O)=[O:22].OO>C(O)(=O)C>[F:1][C:2]1[C:3]([S:12]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)=[O:22])=[N:4][CH:5]=[C:6]([C:8]([F:9])([F:10])[F:11])[CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 784Hydrogen PeroxideHCID 6422Trifluoroacetic acidHCID 184665183-Fluoro-2-phenylthio-5-trifluoromethylpyridine

生成物 1

HCID 184665193-Fluoro-2-phenylsulfinyl-5-trifluoromethylpyridine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
22 °C

実験手順

20 g (0.0693 mol) of 95% pure 3-fluoro-2-phenylthio-5-trifluoromethylpyridine were introduced into 100 ml of glacial acetic acid and 20 ml of trifluoroacetic acid and over a period of 5 min, with stirring at 22° C., 5.64 g (0.083 mol) of 50% strength hydrogen peroxide were added. The reaction mixture was stirred at 22° C. for 10 h and then poured into 1 l of ice-water and extracted with methylene chloride. The organic phase was washed with saturated sodium bicarbonate solution and water. After drying, filtration through silica gel and concentration under reduced pressure, 19.1 g (95.4% of theory) of the title compound of 24 n D

後処理

  1. stirringThe reaction mixture was stirred at 22° C. for 10 h
  2. extractionextracted with methylene chloride
  3. washThe organic phase was washed with saturated sodium bicarbonate solution and water
  4. customAfter drying
  5. filtrationfiltration
  6. concentrationthrough silica gel and concentration under reduced pressure, 19.1 g (95.4% of theory) of the title compound of 24 n D

出典と根拠

ORDレコード
ord-b9b1d0163ddc4a40b4e2f3efd531e50b
出典データセット
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06191280B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート