Beilstein Journal of Organic Chemistry (Oct 2010)

Formation of epoxide-amine oligo-adducts as OH-functionalized initiators for the ring-opening polymerization of ε-caprolactone

  • Julia Theis,
  • Helmut Ritter

DOI
https://doi.org/10.3762/bjoc.6.105
Journal volume & issue
Vol. 6, no. 1
pp. 938 – 944

Abstract

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Epoxide-amine oligo-adducts were synthesized via a one-pot microwave assisted heterogeneous catalytic transfer hydrogenation. Accordingly, 4-nitroanisole was reduced under microwave conditions to give 4-aminoanisole which reacted immediately with the diglycidyl ether of bisphenol A in an addition polymerization reaction to yield oligo(amino alcohol)s. The hydroxy groups of the new formed oligomers were used as the initiator for the ring-opening polymerization of ε-caprolactone to produce a graft copolymer.

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