Dimethylformamide → 2-Chloro-6-fluoro-3-methylbenzaldehyde
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
반응물 6
생성물 1
시약·촉매·용매 2
반응 조건
- 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
- temperaturemaintaining the internal reaction temperature <-70° C
- temperatureThe reaction mixture is cooled
- additionis added dropwise
- customThe resulting reaction mixture
- temperaturecooled
- custompartitioned between dilute aqueous HCl and ether
- washThe organic solution is washed with aqueous NaHCO3
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customtriturated with hexanes
출처 및 근거
- ORD 기록
- ord-836b52912f9942059d71827ee5d90a0e
- 출처 데이터셋
- uspto-grants-1996_01
- 특허 번호
- US05482974
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