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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250991Generated: October 25, 2026

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

https://huagongshe.com/reaction/250991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Cyano-3,5-difluoropyridineHCID 2783253—
SolventDichloromethaneHCID 6344—
Product3,5-Difluoropyridine-2-carbaldehydeHCID 4508348620%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863293B2
Source datasetuspto-grants-2011_01
ORD IDord-f0ed34e6248448be8ca7fb43b1ca901f
Source noteuspto-grants-2011_01