Dimethylformamide → 6-Methyl-3-pyridinecarboxaldehyde

HRID 85186

반응식

HRID 85186 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]([CH3:8])=[N:6][CH:7]=1.[Li]CCCC.CN([CH:17]=[O:18])C>C1COCC1>[CH3:8][C:5]1[CH:4]=[CH:3][C:2]([CH:17]=[O:18])=[CH:7][N:6]=1

참가 물질

5

실험 절차

To a solution of 5-bromo-2-methylpyridine (151; 10 g, 58.1 mmol) in THF (150 mL) was added n-BuLi (2.5 M, 25.6 mL) at −78° C. The reaction mixture was stirred at this temperature for 1 h. DMF (1.30 mL) was then added and the resulting reaction mixture was stirred for 1 h at −78° C. The reaction was quenched by the addition of aq. NH4Cl. Upon warming to room temperature, the mixture was extracted with EtOAc. The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The resulting residue was purified by chromatography to afford 6-methylnicotinaldehyde 152 (5.0 g, 72%).

후처리

  1. customthe resulting reaction mixture
  2. stirringwas stirred for 1 h at −78° C
  3. customThe reaction was quenched by the addition of aq. NH4Cl
  4. extractionthe mixture was extracted with EtOAc
  5. dry with materialThe combined organic layers were dried (Na2SO4)
  6. concentrationconcentrated under reduced pressure
  7. customThe resulting residue was purified by chromatography

출처 및 근거

ORD 기록
ord-2b79cc6d18e6464aaf106b76420e7363
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08846947B2

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