| Literature DB >> 26235971 |
Shanmugam Thiyagarajan1,2, Homer C Genuino1, Michał Śliwa1, Jan C van der Waal3, Ed de Jong4, Jacco van Haveren2, Bert M Weckhuysen1, Pieter C A Bruijnincx5, Daan S van Es6.
Abstract
A novel route for the production of renewable aromatic chemicals, particularly substituted phthalic acid anhydrides, is presented. The classical two-step approach to furanics-derived aromatics via Diels-Alder (DA) aromatization has been modified into a three-step procedure to address the general issue of the reversible nature of the intermediate DA addition step. The new sequence involves DA addition, followed by a mild hydrogenation step to obtain a stable oxanorbornane intermediate in high yield and purity. Subsequent one-pot, liquid-phase dehydration and dehydrogenation of the hydrogenated adduct using a physical mixture of acidic zeolites or resins in combination with metal on a carbon support then allows aromatization with yields as high as 84 % of total aromatics under relatively mild conditions. The mechanism of the final aromatization reaction step unexpectedly involves a lactone as primary intermediate.Entities:
Keywords: Diels-Alder reaction; aromatics; aromatization; furans; hydrogenation
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Year: 2015 PMID: 26235971 DOI: 10.1002/cssc.201500511
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928