Elucidation of a polychlorinated bipyrrole structure using enantioselective GC.

A hexachloro congener (Q1-hex) of the natural heptachloro-1'-methyl-1,2'-bipyrrole Q1 was recently observed as a byproduct of the Q1 synthesis. NMR investigation confirmed that Q1-hex has a proton on a carbon in beta-position to a nitrogen. Three isomers are possible that fulfill this prerequisite; unfortunately, however, the NMR data were not sufficient to distinguish among the three structural variants. Because only one isomer of Q1-hex is expected to be chiral, we utilized enantioselective gas chromatography and two chiral stationary phases to separate the atropisomers. Baseline separation of the Q1-hex atropisomers was obtained on 10% chemically bonded permethyl-beta-cyclodextrin. In the full-scan mode, it was found that Q1-hex was racemic and that both atropisomers had identical mass fragmentation patterns. Partial resolution of the Q1-hex atropisomers was obtained on 25% tert-butyldimethylsilylated beta-cyclodextrin diluted in PS086. In concert with previous NMR data, these enantioseparations prove that the structure of Q1-hex is 2,3,3',4',5,5'-hexachloro-1'-methyl-1,2'-bipyrrole (5). To our knowledge, this is the first gas chromatographic separation of atropisomers of an axially chiral 1,2'-bipyrrole derivative.