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Potassium Nitrate → 5-Nitro-2-(trifluoromethyl)quinoline

HRID 2182690
ノート
印刷プレビュー

反応式

HRID 2182690 の反応式
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1.[N+:15]([O-])([O-:17])=[O:16].[K+]>S(=O)(=O)(O)O>[N+:15]([C:9]1[CH:8]=[CH:7][CH:6]=[C:5]2[C:10]=1[CH:11]=[CH:12][C:3]([C:2]([F:1])([F:13])[F:14])=[N:4]2)([O-:17])=[O:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24434Potassium NitrateHCID 27778052-(Trifluoromethyl)quinoline

生成物 1

HCID 219488215-Nitro-2-(trifluoromethyl)quinoline

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

1.52 g (7.7 mmol) of 2-(trifluoromethyl)quinoline is dissolved in 7.90 ml of concentrated sulfuric acid, and 1.47 g of potassium nitrate is added in portions at 0° C. After 20 hours at room temperature, the reaction solution is poured onto ice/water. It is extracted with ethyl acetate, the combined organic phases are washed with saturated sodium bicarbonate solution and dried on sodium sulfate. After removal of the solvent and chromatography on silica gel with hexane-ethyl acetate (10-100%), 390 mg (21% of theory) of the product is obtained.

後処理

  1. additionthe reaction solution is poured onto ice/water
  2. extractionIt is extracted with ethyl acetate
  3. washthe combined organic phases are washed with saturated sodium bicarbonate solution
  4. customdried on sodium sulfate
  5. customAfter removal of the solvent and chromatography on silica gel with hexane-ethyl acetate (10-100%), 390 mg (21% of theory) of the product
  6. customis obtained

出典と根拠

ORDレコード
ord-018a70e67d1846058801aef872484d26
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06897224B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート