Hydrogen Bromide → 1-(2-Bromopyridin-4-yl)-2-(4-fluorophenyl)ethanone

HRID 429200

반응식

HRID 429200 반응식
Cl[C:2]1[CH:7]=[C:6]([C:8](=[O:19])[CH:9](C#N)[C:10]2[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=2)[CH:5]=[CH:4][N:3]=1.[BrH:20]>C(=O)(O)[O-].[Na+]>[Br:20][C:2]1[CH:7]=[C:6]([C:8](=[O:19])[CH2:9][C:10]2[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=2)[CH:5]=[CH:4][N:3]=1

참가 물질

4

반응 조건

온도
135 °C

실험 절차

To 1-(2-chloropyridin-4-yl)-2-cyano-2-(4-fluorophenyl)ethanone (22.0 g, 80 mmol) was added 48% hydrobromic acid (75 ml) and the reaction mixture was heated at reflux in an oil bath at 135° C. After 4 h, the reaction mixture was allowed to cool to room temperature and then further cooled in an ice bath. Saturated sodium bicarbonate (100 ml) was carefully added, followed by solid portions of sodium bicarbonate until the pH of the reaction mixture was neutral. The reaction mixture was then extracted with ethyl acetate and the ethyl acetate layer was dried over sodium sulfate, filtered and concentrated to a brown semi-solid (2.8 g). The crude product was purified by flash chromatography on silica gel, eluting with 1:1 mixture of ethyl acetate/hexanes to give 1-(2-bromopyridin-4-yl)-2-(4-fluorophenyl)ethanone (1.9 g).

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureto cool to room temperature
  3. temperaturefurther cooled in an ice bath
  4. extractionThe reaction mixture was then extracted with ethyl acetate
  5. dry with materialthe ethyl acetate layer was dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to a brown semi-solid (2.8 g)
  8. customThe crude product was purified by flash chromatography on silica gel
  9. washeluting with 1:1 mixture of ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-eab152bfa51b4349aa18c7d849f7cdb2
출처 데이터셋
uspto-grants-2001_11
특허 번호
US06316464B1

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