Novel reaction of 3, 4-dibromofuran with azo diesters to give tetrahydropyridazinones. Issue 27 (29th February 2016)

• Record Type: Journal Article
• Authors: Aitken, Kati M.; Aitken, R. Alan; Slawin, Alexandra M. Z.
• Is Part Of: RSC advances. Volume 6:Issue 27(2016)
• Page Start: 22969
• Page End: 22972
• Publication Date: 2016-02-29
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra02735k
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Diels–Alder cycloaddition followed by rearrangement gives unexpected heterocyclic products whose structure is investigated by variable-temperature NMR spectroscopy and X-ray diffraction. Abstract : Cycloaddition of 3, 4-dibromofuran with azo diesters proceeds by a Diels–Alder reaction followed by a novel rearrangement to give 3, 5-dibromotetrahydropyridazin-4-ones. Variable-temperature NMR spectroscopy shows four separate conformations at low temperature attributed to restricted rotation about the carbamate functions. The ethyl compound decomposes upon storage with loss of the carbamate groups and aromatisation to give a simple bromohydroxypyridazinium salt.