Issue 11, 2006

Synthesis of bis(azafulvene)s by dehydration of hydroxymethylpyrrole derivatives

Abstract

Bis(azafulvene) was isolated in 55% yield by the reaction of 4 equivalents of phenyllithium with 5,5′-diformyl-3,3′,4,4′-tetraethyl-2,2′-bipyrrole followed by quenching with acetic anhydride. Unstable bis(azafulvene)s were obtained in much higher yields by dehydrating 5,5′-bis(hydroxymethyl) derivatives of 2,2′-bipyrrole and gem-dimethyl-2,2′-dipyrrylmethane with (Boc)2O–DMAP at room temperature. X-Ray crystallography of two bis(azafulvene)s is reported.

Graphical abstract: Synthesis of bis(azafulvene)s by dehydration of hydroxymethylpyrrole derivatives

Supplementary files

Article information

Article type
Paper
Submitted
03 Jan 2006
Accepted
07 Apr 2006
First published
03 May 2006

Org. Biomol. Chem., 2006,4, 2247-2252

Synthesis of bis(azafulvene)s by dehydration of hydroxymethylpyrrole derivatives

J. Setsune, A. Tanabe, J. Watanabe and S. Maeda, Org. Biomol. Chem., 2006, 4, 2247 DOI: 10.1039/B518340E

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