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Chemical Upcycling of Waste Poly(bisphenol A carbonate) to 1,4,2‐Dioxazol‐5‐ones and One‐Pot C−H Amidation

Hyun Jin Jung, Sora Park, Hyun Sub Lee, Hyun Gyu Shin, Yeji Yoo, Ek Raj Baral, Jun Hee Lee, Jaesung Kwak, Jeung Gon Kim

2021ChemSusChem21 citationsDOI

Abstract

Chemical upcycling of poly(bisphenol A carbonate) (PC) was achieved in this study with hydroxamic acid nucleophiles, giving rise to synthetically valuable 1,4,2-dioxazol-5-ones and bisphenol A. Using 1,5,7-triazabicyclo[4.4.0]-dec-5-ene (TBD), non-green carbodiimidazole or phosgene carbonylation agents used in conventional dioxazolone synthesis were successfully replaced with PC, and environmentally harmful bisphenol A was simultaneously recovered. Assorted hydroxamic acids exhibited good-to-excellent efficiencies and green chemical features, promising broad synthetic application scope. In addition, a green aryl amide synthesis process was developed, involving one-pot depolymerization from polycarbonate to dioxazolone followed by rhodium-catalyzed C-H amidation, including gram-scale examples with used compact discs.

Topics & Concepts

Bisphenol APhosgeneChemistryDimethyl carbonateBisphenolOrganic chemistryDiphenyl carbonateGreen chemistryAmideCarbonateDepolymerizationArylNucleophileCatalysisCarbonylationEpoxyReaction mechanismTransesterificationCarbon monoxideAlkylCarbon dioxide utilization in catalysisSynthetic Organic Chemistry MethodsChemistry and Chemical Engineering
Chemical Upcycling of Waste Poly(bisphenol A carbonate) to 1,4,2‐Dioxazol‐5‐ones and One‐Pot C−H Amidation | Litcius