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

Temperature

-78 °C

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).

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

ORD record

ord-f0ed34e6248448be8ca7fb43b1ca901f

Source dataset

uspto-grants-2011_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07863293B2