Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11562Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/11562

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
PatentnummerUS07098236B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-f62c3c18b80740c0b6b9fd0839671267
Quellennotizuspto-grants-2006_08