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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 250991Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/250991

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiisobutylaluminum hydrideHCID 14487—
EduktSodium BicarbonateHCID 516892—
Edukt2-Cyano-3,5-difluoropyridineHCID 2783253—
LösungsmittelDichloromethaneHCID 6344—
Produkt3,5-Difluoropyridine-2-carbaldehydeHCID 4508348620%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863293B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-f0ed34e6248448be8ca7fb43b1ca901f
Quellennotizuspto-grants-2011_01