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

HRID 2182690
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HRID 2182690 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24434Potassium NitrateHCID 27778052-(Trifluoromethyl)quinoline

생성물 1

HCID 219488215-Nitro-2-(trifluoromethyl)quinoline

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-018a70e67d1846058801aef872484d26
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06897224B2

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