Dimethylformamide → 2-Chloro-6-fluoro-3-methylbenzaldehyde

HRID 374954노트

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HRID 374954 반응식
C([Li])(CC)C.C1CCCCC1.[C:12](=[O:14])=O.CC(C)=O.CN(CCN(C)C)C.[Cl:27][C:28]1[CH:33]=[C:32]([F:34])[CH:31]=[CH:30][C:29]=1[CH3:35].CN(C=O)C>C1COCC1.CCOCC>[F:34][C:32]1[CH:31]=[CH:30][C:29]([CH3:35])=[C:28]([Cl:27])[C:33]=1[CH:12]=[O:14]

참가 물질

9

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온도
-30 °C

실험 절차

A solution of 1.3M s-butyl lithium in cyclohexane (75 mL, 98 mmol) is added to a dry-ice/acetone cooled solution of TMEDA (9.67 g, 83 mmol) in THF (90 mL), maintaining the internal reaction temperature <-70° C. The reaction mixture is cooled and maintained at ≤-80° C. with an ether/liquid nitrogen bath while a solution of 2-chloro-4-fluorotoluene (10 g, 69 mmol) in THF (10 mL) is added dropwise. The resulting reaction mixture is stirred with dry-ice/acetone cooling for 1h, then is cannulated into an ether/liquid nitrogen cooled and mechanically stirred solution of DMF (25.1 g, 345 mmol) in THF (50 mL). The resulting mixture is warmed to -30° C. and partitioned between dilute aqueous HCl and ether. The organic solution is washed with aqueous NaHCO3, dried (MgSO4), and concentrated and triturated with hexanes to afford 2-fluoro-5-methyl-6-chlorobenzaldehyde as a crystalline solid.

후처리

  1. temperaturemaintaining the internal reaction temperature <-70° C
  2. temperatureThe reaction mixture is cooled
  3. additionis added dropwise
  4. customThe resulting reaction mixture
  5. temperaturecooled
  6. custompartitioned between dilute aqueous HCl and ether
  7. washThe organic solution is washed with aqueous NaHCO3
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated
  10. customtriturated with hexanes

출처 및 근거

ORD 기록
ord-836b52912f9942059d71827ee5d90a0e
출처 데이터셋
uspto-grants-1996_01
특허 번호
US05482974

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