Polydepsipeptides, copolymers of α - amino acids and α - hydroxy acids, could prove to be a valuable new class of synthetic biodegradable polymers. In this paper, steps in synthesis of poly (dl-lactide-co-3, 6-dimethylmorpholine-2,5-dione) from dl-Iactide and dl-3,6-dimethylmorpholine-2,5-dione was explained. dl -Lactide was synthesized from lactic acid. In the reaction of 2-bromopropionyl chloride and dl-alanine, N-(2-bromopropionyl)-dl-alanine was prepared and this material was converted to its salt and finally this salt was converted to 3, 6-dimethylmorpholine-2, 5-dione in a sublimer. These two monomers, that is, dl -lactide and dl-3, 6-dimethylmorpholine-2, 5-dione was polymerized by ring-opening polymerization. FT-IR, 1H NMR, 13C NMR Spectra were used for structure elucidation of all intermediate compounds and final product.