Synthesis of photochromic 2,3-bis(2,5-dimethyl-3-thienyl)-3-cyanoacrylates by the Beckmann rearrangement of a cyclobutenedione derivative
An unusual Beckmann rearrangement was discovered in the reaction of 3,4-bis(2,5-dimethyl-3-thienyl)cyclobut-3-ene-1,2-dione with hydroxylamine hydrochloride to give esters of 2,3-bis(2,5-dimethyl-3-thienyl)-3- cyanoacrylic acid.
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Veröffentlicht in: | Mendeleev communications 2004, Vol.14 (5), p.202-204 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | An unusual Beckmann rearrangement was discovered in the reaction of 3,4-bis(2,5-dimethyl-3-thienyl)cyclobut-3-ene-1,2-dione with hydroxylamine hydrochloride to give esters of 2,3-bis(2,5-dimethyl-3-thienyl)-3- cyanoacrylic acid. |
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ISSN: | 0959-9436 |
DOI: | 10.1070/MC2004v014n05ABEH001916 |