Hydrochloric Acid → 3,5-Difluoropyridine-2-carbaldehyde

HRID 250991

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HRID 250991 반응식
[F:1][C:2]1[C:3]([C:9]#N)=[N:4][CH:5]=[C:6]([F:8])[CH:7]=1.CC(C[AlH]CC(C)C)C.Cl.C([O-])(O)=[O:22].[Na+]>C(Cl)Cl>[F:1][C:2]1[C:3]([CH:9]=[O:22])=[N:4][CH:5]=[C:6]([F:8])[CH:7]=1

참가 물질

6

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온도
-78 °C

실험 절차

To a solution of 3,5-difluoro-pyridine-2-carbonitrile (0.440 g, 3.14 mmol) (Niewoehner, U. et al. PCT Int. Appl. (2001), WO 2001068647) in dry CH2Cl2 (20 mL) cooled at −78° C., was added DIBAL-H (1.0 M in CH2Cl2, 3.2 mL, 3.2 mmol). After the mixture was stirred at −78° C. for 1 h, aqueous HCl (3 N, 10 mL) was added, and the mixture was warmed to room temperature. Saturated aqueous NaHCO3 (20 mL) was added, and the mixture was extracted with CH2Cl2 (3×20 mL). The extracts were combined and dried over anhydrous Na2SO4. After filtration the solvent was removed by evaporation under vacuum, and the residue was purified by flash chromatography on a silica gel column (CH2Cl2), affording afford 3,5-difluoro-pyridine-2-carbaldehyde as a colorless crystalline solid (0.0880 g, 20%). 1H NMR (CDCl3) δ 7.32-7.39 (m, 1H), 8.53 (d, 1H, J=2.4 Hz), 10.16 (s, 1H).

후처리

  1. temperaturethe mixture was warmed to room temperature
  2. extractionthe mixture was extracted with CH2Cl2 (3×20 mL)
  3. dry with materialdried over anhydrous Na2SO4
  4. filtrationAfter filtration the solvent
  5. customwas removed by evaporation under vacuum
  6. customthe residue was purified by flash chromatography on a silica gel column (CH2Cl2)
  7. customaffording

출처 및 근거

ORD 기록
ord-f0ed34e6248448be8ca7fb43b1ca901f
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07863293B2

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