Currently, amidst atmospheric menace where natural calamities
such
as wildfire and floods are becoming more frequent than ever, biobased
derivatives offer a sustainable alternative to conventional ways,
for instance, petrochemical commodities. Biobased products, obtained
from agricultural waste, including 5-(hydroxymethyl)furfural (HMF),
2,5-bis(hydroxymethyl)furan (BHMF), and 2,5-furandicarboxylic acid
(FDCA) are promising chemical platforms in the biorefinery, which
is yet to be explored. The Diels–Alder cycloaddition of BHMF
and N-phenylmaleimide derivatives under optimal reaction
conditions is investigated in this report. First, HMF is reduced to
BHMF in the presence of NaBH4, and then the Diels–Alder
reaction of BHMF and N-phenylmaleimide derivatives
is investigated to produce Diels–Alder adducts. All novel compounds
are synthesized in acceptable yields and effectively characterized
by employing important techniques such as one-dimensional (1D) NMR
spectroscopy (1H, 13C, DEPT-90, and DEPT- 135),
two-dimensional (2D) NMR spectroscopy (1H–1H COSY, 1H–13C HSQC, and 1H–13C HMBC), IR spectroscopy, elemental analysis,
mass spectrum (QTOF), and single-crystal X-ray diffraction (SC-XRD).
Furthermore, this study underlines the necessity of sustainable synthetic
methodologies and gives critical insights into the progress of ecologically
friendly methodologies, providing a new avenue as a tunable precursor
for the challenging functionalized polymer in the future.