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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 83113Erstellt: 23. Oktober 2026

Sodium Chloride → 2-Methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridine

https://huagongshe.com/de/reaction/83113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktSodium hydrideHCID 24758—
Edukt2-Fluoro-6-methylpyridineHCID 96090—
Edukt(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridineHCID 5751983148,2%

Reaktionsschritte

To a suspension of sodium hydride (55% dispersion in mineral oil, 48 mg, 1.1 mmol) in THF (1.5 mL) was added a solution of (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (189 mg, 1.0 mmol) in THF (3 mL) at 0° C. and the reaction mixture warmed to room temperature over 30 min. Then a solution of 2-fluoro-6-methylpyridine (122 mg, 1.1 mmol) in THF (3 mL) was added dropwise at 0° C. and the reaction mixture was stirred at room temperature overnight. The reaction mixture was then poured into aqueous sodium chloride (saturated) and the mixture was extracted with ethyl acetate. The combined organic layers were then washed with water and brine and then dried over sodium sulfate, filtered and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 4:1) afforded the title compound (135 mg, 48%) which was obtained as a yellow oil. MS: m/e=281.1 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846719B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-97dc3e647fb34eddb9b3a2979bd6cb4a
Quellennotizuspto-grants-2014_09