Sodium Nitrate → 5-fluoro-2-methoxypyridine

HRID 1932292노트

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HRID 1932292 반응식
N[C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1.[N+]([O-])([O-])=O.[Na+].[F:15][P-](F)(F)(F)(F)F.[H+]>Cl.O>[F:15][C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1

참가 물질

6

실험 절차

5-amino-2-methoxypyridine (81.5 g, 0.657 mol) was dissolved in a mixture of concentrated hydrochloric acid (120 ml) and water (530 ml). A solution of sodium nitrate (56.5 g, 0.819 mol) in water (100 ml) was added at −5° C. to the solution. The reaction mixture was stirred for 45 minutes at room temperature and sodium nitrate (56.5 g, 0.819 mol) was further added thereto. Hexafluorophosphoric acid (132 ml) was added to the reaction mixture, which was then stirred for 20 minutes at room temperature. The reaction mixture was filtered to obtain a solid, which was washed with water and ethyl ether and then dried under reduced pressure. The resulting compound was heated for 15 minutes at 150° C., dissolved in dichloromethane, and then washed with 3N sodium hydroxide solution. The organic layer was dried on anhydrous magnesium sulfate, concentrated under reduced pressure, and then fractionally distilled to give 22.6 g of the titled compound as colorless oil. (Yield: 27%).

후처리

  1. stirringwas then stirred for 20 minutes at room temperature
  2. filtrationThe reaction mixture was filtered
  3. customto obtain a solid, which
  4. washwas washed with water and ethyl ether
  5. customdried under reduced pressure
  6. temperatureThe resulting compound was heated for 15 minutes at 150° C.
  7. dissolutiondissolved in dichloromethane
  8. washwashed with 3N sodium hydroxide solution
  9. dry with materialThe organic layer was dried on anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. distillationfractionally distilled

출처 및 근거

ORD 기록
ord-b5b7fc632b394349b3241fa75290883d
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08188114B2

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