With the aim to investigate
new strategies for upcycling
of plastic
waste, we performed aminolysis of poly(lactic acid) (PLA), using
N,N
-dimethylethylenediamine (DMEDA),
N
,
N
-dimethylpropylenediamine (DMPDA), and 3-aminopropylimidazole
(API) as nucleophiles. The
N
-substituted lactamides
obtained were alkylated by using alkyl halides differing in alkyl
chain length, obtaining organic salts that in most cases behaved as
ionic liquids (ILs). Both aminolysis of PLA and alkylation of amides
were carried out taking into consideration the basic principles of
the holistic approach to green chemistry, applied at a laboratory
scale, and carefully selecting the nature of the reaction solvent,
temperature range, and amount of reagents. Organic salts obtained
from the alkylation of
N
-substituted lactamides were
investigated to determine their glass or solid–liquid transitions
and their thermal stability. Furthermore, cytotoxicity toward normal
lung fibroblasts was also assessed. Data collected show that the proposed
strategy represents a valuable protocol to upcycle plastic waste,
using it as starting material to obtain alternative solvents of potential
industrial relevance.