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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128684Erstellt: 24. Oktober 2026

3-Phenoxybenzoic acid → 5-Acetyl-4-methyl-2-(3-phenoxyphenyl)oxazole

https://huagongshe.com/de/reaction/128684

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Phenoxybenzoic acidHCID 19539—
Edukt3-PhenoxybenzamideHCID 16618625—
LösungsmittelSodium HydroxideHCID 14798—
Produkt5-Acetyl-4-methyl-2-(3-phenoxyphenyl)oxazoleHCID 1937492894%

Reaktionsbedingungen

Temperatur180 °C

Reaktionsschritte

A mixture of 3-phenoxybenzamide (2.13 g, 10 mmol), 3-phenoxybenzoic acid (4.28 g, 20 mmol), and 3-chloropenta-2,4-dione (0.44 g, 3.3 mmol) was heated to 180° C. under stirring for 23 h. The hot mixture was poured into 1N aqueous sodium hydroxide (100 ml), and extracted with diethyl ether (100+2×50 ml). The combined organic phases were washed with saturated aqueous sodium bicarbonate (50 ml) and brine (50 ml), dried over magnesium sulfate, and evaporated to dryness. Purification by silica gel column chromatography (135 g, 16.7% ethyl acetate in n-hexane) afforded the titled compound as solids in 94% yield: 1H NMR (CDCl3) δ7.88-7.83 (1H, m), 7.77-7.53 (1H, m), 7.49-7.34 (3H, m), 7.18-7.12 (2H, m), 7.07-7.00 (2H, m), 2.55 (3H, s), 2.54 (3 H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05464849
Quelldatensatzuspto-grants-1995_11
ORD IDord-73a8b1f0a08048a8937510601d49b623
Quellennotizuspto-grants-1995_11