<b>Targeted Intermediates of Eudesmic Acid Synthesis and X ray Investigations</b> it was carried out synthesis of esters and their dinitro derivatives of 3,4,5 trimethoxybenzoic eudesmic acid. Esterification of eudesmic acid carried out n absolute methanol or ethanol and corresponding methyl and ethyl 3,4,5 trimethoxybenzoates 2, 3 have been synthesized in good yields. It was revealed that nitration of these esters gives only dinitro products. The structure of the synthesized compounds of the methyl and ethyl 2,6 dinitro 3,4,5 trimethoxybenzoates 4, 5 was determined by X ray diffraction analysis XRD . In the asymmetric part of the crystal structures of 4, 5 one and two molecules are observed, respectively. In crystalline structures a flat nitro groups and carboxylic groups do not participate in the conjugation with aromatic rings. In the crystal structure of 4, an intermolecular C8 H...O9 hydrogen bond is observed, these H bonds link the molecules along the 010 axis. In the crystal structure of 5, intermolecular C9B H...O4A and C10B H...O8A hydrogen bonds form chains along the 011 axis. The formed chains are cross linked by the intermolecular C9B H...O5A hydrogen bonds. synthesis methyl and ethyl 3,4,5 trimethoxybenzoates methyl and ethyl 2,6 dinitro 3,4,5 trimethoxybenzoates esterification nitration X ray diffraction analysis. 176-181 Issue-6 Volume-1 Olimova M.I. | Okmanov R. Ya. | Elmuradov B. Zh.