RESUMEN
The title compound, C40H41NO8, is a product of the reduction of the cyclic carbonyl group of the γ-piperidone subunit of the aza-14-crown-4 ether with subsequent re-esterification of its dimethyl butenoate substituent into a monoethyl monomethyl group. The aza-crown macrocycle exhibits a bowl conformation with a dihedral angle of 70.82â (5)° between the benzene rings fused to it. The piperidine ring adopts a chair conformation and the methyl ethyl ethyl-enedi-carboxyl-ate fragment has a cis conformation, with a dihedral angle of 66.51â (7)° between the two carboxyl-ate groups. The ethyl group is disordered over two sites with occupancies of 0.70â (1):0.30â (1). In the crystal, mol-ecules form inversion dimers, via pairs of O-Hâ¯O hydrogen bonds, that stack along the a axis.