BACKGROUND: AROMATIC CONDENSED OXAZINONE DERIVATIVES HAVE RECEIVED CONSIDERABLE ATTENTION DUE TO THE ATTRACTIVE PHARMACOLOGICAL PROPERTIES ASSOCIATED WITH THEIR HETEROCYCLIC SCAFFOLD [1]. NAPHTHOXAZINE, AN IMPORTANT MOTIF IN HETEROCYCLIC CHEMISTRY, HAS REPORTED CYTOTOXIC AND ANTIFUNGAL ACTIVITIES [2]. THEREFORE, DEVELOPMENT OF SIMPLE, ROBUST AND SAFER METHODOLOGIES FOR THE SYNTHESIS OF NAPHTHOXAZINONE DERIVATIVES IS OF PRIME INTEREST FOR OBTAINING THESE PRODUCTS UNDER CONDITIONS TOLERATED BY SENSITIVE FUNCTIONAL GROUPS FROM BOTH SYNTHETIC AND ENVIRONMENTAL POINTS OF VIEW. THE ROLE OF COPPER NANOPARTICLES IN COUPLING CHEMISTRY HAS BEEN WELL DOCUMENTED [3-4].METHODS: AN EFFICIENT PROTOCOL FOR THE SYNTHESIS OF 2-NAPHTHOL-CONDENSED 1, 3-OXAZINONE, (SCHEME1) BY THE REACTION BETWEEN BENZALDEHYDE, UREA, AND B-NAPHTHOL, WAS CARRIED OUT IN THE PRESENCE OF NA2CO3 AND COPPER FERRITE NANOPARTICLES STABILIZED BY PEG-400. THE PROGRESS OF THE REACTION WAS MONITORED BY TLC, AND THE PRODUCTS PURIFICATION THE CHARACTERIZED BY 1H NMR, 13C NMR, FT-IR AND MASS ANALYSIS.RESULTS: IN THE ABSENCE OF CU, THE REACTION WAS NOT INITIATED. WHEN THE SAME REACTION WAS CARRIED OUT WITHOUT PEG- 400, THE YIELD WAS ONLY 30%, THE IDEAL SOLVENT FOR THIS SYNTHESIS IS PEG-400. BECAUSE IT ACTS AS A SOLVENT AND CU NANOPARTICLES STABILAZER.CONCLUSION: THIS PROCESS IS SIMPLE, COST EFFECTIVE, GREEN AND ECO-FRIENDLY AS IT IS A ONE-POT SYNTHESIS WITH EASY WORKUP AND DOES NOT REQUIRE SPECIAL CONDITIONS SUCH AS ELEVATED TEMPERATURE AND HARSH REAGENTS, ALSO NEEDS LESSER QUANTITY OF CATALYST (USUALLY MG) AND THE COPPER-NANOPARTICLES CAN BE USED TO AN EFFICIENT RECYCLABLE MEDIUM.