2-Aryl-3-alkoxycarbonyl chromones were effectively constructed from aryl aldehydes and 3- (2-(methoxymethoxy) phenyl) propiolates via a cascade Lewis acid catalyzed phenol ether deprotection/aldehyde olefination/intramolecular oxa-Michael addition reaction, and a sequential oxidation. This four-step reaction could be conducted in one-pot with high atom efficiency.