A one-pot, one-catalyst, sequential ring-opening transesterification polymerization (ROTEP) was used to prepare fully renewable amorphous poly(D,L-lactide)−poly(ε-decalactone)−poly(D,L-lactide) (LDL) triblock polymers. These α,ω hydroxy-telechelic polymers were subsequently coupled to prepare linear alternating (LDL) n multiblock polymers. Differential scanning calorimetry (DSC) and small-angle X-ray scattering (SAXS) indicated microphase separation into two domains in both the triblock and multiblock architectures. The temperature dependent Flory−Huggins interaction parameter for this system, χ(T) = 69.1/T − 0.072, was estimated from the experimentally determined order−disorder transition temperature (T ODT ) values of four symmetric LDL triblock polymers. Uniaxial extension tests revealed a dramatic dependence of the room-temperature mechanical properties on overall molar mass. Additionally, coupling low molar mass LDL triblocks to prepare (LDL) n multiblocks led to substantial increases in the ultimate elongation and tensile stress at break. Compared to high molar mass triblocks with inaccessible T ODT values, (LDL) n multiblocks of similar composition and molar mass were found to disorder at much lower temperatures (T ODT < 150°C). Because of this, it was possible to process (LDL) n using injection molding. The simple synthetic procedure and melt processability of the (LDL) n multiblock polymers make these multiblocks attractive as renewable thermoplastic elastomers (TPEs).