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HRID 220481Erstellt: 25. Oktober 2026

Sodium hydride → 1-(3,5-Dimethylisoxazol-4-ylmethyl)-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/220481

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktIsoxazole, 4-(chloromethyl)-3,5-dimethyl-HCID 88246—
Edukt1H-pyrazole-4-carbaldehydeHCID 5130673—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(3,5-Dimethylisoxazol-4-ylmethyl)-1H-pyrazole-4-carbaldehydeHCID 86641653—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Add N,N-dimethylformamide (3 mL) to sodium hydride (0.092 g, 2.29 mmol) and stir at 0° C. Add 1-H-pyrazole-4-carboxaldehyde (0.200 g, 2.08 mmol) and stir at 0° C. for 20 min. Dissolve 4-chloromethyl-3,5-dimethylisoxazole (0.318 g, 2.18 mmol) in N,N-dimethylformamide (4 mL) and add to reaction mixture. Stir reaction at room temperature for 18 hr. Quench with aqueous saturated sodium bicarbonate solution. Add ethyl acetate and separate organic layer. Extract aqueous layer twice with ethyl acetate. Dry combined organic layers (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 25:75 to 75:25 ethyl acetate:hexanes), to give the title preparation (387 mg, 91%). GC-MS: m/z=205 [M+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202873B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-b49960dd7d97476f83026d6423df702e
Quellennotizuspto-grants-2012_06