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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2219187Erstellt: 26. Oktober 2026

(4-Nitrophenyl)acetic acid → 1-(4-Morpholinyl)-2-(4-nitrophenyl)ethanone

https://huagongshe.com/reaction/2219187

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Nitrophenyl)acetic acidHCID 4661—
EduktMorpholineHCID 8083—
EduktSodium BicarbonateHCID 516892—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(4-Morpholinyl)-2-(4-nitrophenyl)ethanoneHCID 5170165—

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

A room temperature solution of 1.8839 gms. (4-Nitro-phenyl)-acetic acid in tetrahydrofuran (5 mL) is treated with 1.8069 gms. 1′,1′-carbonyl-diimidizole. The reaction mixture is stirred for 1 h. The reaction mixture is then treated with 1.0 mL morpholine. The reaction is heated overnight at 35° C. The reaction is then allowed to cool to room temperature, and is made basic with the addition of saturated aqueous sodium bicarbonate. The resulting mixture is extracted with ethyl acetate. The aqueous layer is re-extracted four more times with ethyl acetate. The combined organics are evaporated to dryness in vacuo. The crude product residue is then chromatographed by flash silica gel chromatography using 60% ethyl acetate in hexanes as the eluant. Following evaporation of solvent, 1-morpholin-4-yl-2-(4-nitro-phenyl)-ethanone is isolated as a white solid in the amount of 1.4009 gms.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07414054B2
Quelldatensatzuspto-grants-2008_08
ORD IDord-2fbf54534b02460899091b2826bc383b
Quellennotizuspto-grants-2008_08