Abstract
In this work, we addressed the challenge of using chitin-derived furans, 3-acetamido-5-ethylfuran (3A5EF) and 3-acetamido-5-(1-hydroxyethyl)furan (3A5HF), for the formation of 4-acetylaminophthalimides and other N-containing aromatic compounds. The transformation is carried out sequentially and involves the formation of the DA adduct, 7-oxa-norbornene, which in an acidic/acetylating medium undergoes a dehydration/aromatization process providing nitrogenated aromatic compounds in yields ranging from 16–80%. To the best of our knowledge, this is the first report involving a chitin derivative for the formation of 4-acetylaminophthalimides, which is the first step towards expanding the toolbox of chitin-derived furans in the synthesis of nitrogenated aromatic compounds with the nitrogen atom directly attached to the benzene ring.
Supplementary materials
Title
Supporting Information
Description
Electronic Supplementary Information (ESI) available: General Procedures, NMR spectrum, HRMS data, FTIR (ATR) and Theoretical model and computational methods.
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