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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349924Erstellt: 25. Oktober 2026

Water → 4-[3-methyl-1-(2-pyridyl)-1H-pyrazol-4-ylmethoxy]benzaldehyde

https://huagongshe.com/reaction/349924

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt4-FluorobenzaldehydeHCID 68023—
Edukt[3-Methyl-1-(pyridin-2-yl)-1H-pyrazol-4-yl]methanolHCID 23076503—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[3-methyl-1-(2-pyridyl)-1H-pyrazol-4-ylmethoxy]benzaldehydeHCID 8676041886%

Reaktionsschritte

Sodium hydride (60%, oily, 0.80 g) was added to a solution of [3-methyl-1-(2-pyridyl)-1H-pyrazol-4-yl]methanol (3.20 g) in N,N-dimethylformamide (50 ml) at 0° C., and the mixture was stirred at room temperature for one hour. 4-fluorobenzaldehyde (2 ml) was added to the reaction mixture, and the mixture was stirred overnight at 50° C. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and then concentrated. The residue was subjected to silica gel column chromatography, and 4-[3-methyl-1-(2-pyridyl)-1H-pyrazol-4-ylmethoxy]benzaldehyde (4.26 g, yield: 86%) was obtained as colorless crystals from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 84–85° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179823B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-89a4efc031f442a183adb41a574dc0ee
Quellennotizuspto-grants-2007_02