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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219187Generated: October 25, 2026

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

https://huagongshe.com/reaction/2219187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenyl)acetic acidHCID 4661—
ReactantMorpholineHCID 8083—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Morpholinyl)-2-(4-nitrophenyl)ethanoneHCID 5170165—

Reaction Conditions

Temperature35 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414054B2
Source datasetuspto-grants-2008_08
ORD IDord-2fbf54534b02460899091b2826bc383b
Source noteuspto-grants-2008_08