Crystal structure of rac-(3a'R,9a'R)-3a'-(indol-3-yl)-1′,2′,3′,3a',4′,9a'-hexahydrospiro[cyclopentane-1,9′-pentaleno[1,2-b]indole] p-xylene hemisolvate
The title compound, C26H26N2·0.5C8H10, is the first reported characterized 2:2 product from acid-catalyzed condensation of indole with cyclopentanone and no other 2:2 products were observed. Recrystallization from p-xylene gave the title hemisolvate with the p-xylene molecule located about an inversion center. The terminal pentalene ring is envelope-flap disordered at the C atom farthest from the skeletal indole unit, with a refined occupancy ratio of 0.819 (4):0.181 (4). The major component has this C atom bent away from the spiro-fused cyclopentane ring. In the crystal, molecules are connected by N—H...π interactions, forming chains along , and N—H...π and C—H...π interactions, forming chains along , which results in the formation of slabs parallel to (010).
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Document Type: Research Article
Affiliations: Department of Chemistry, University of Minnesota, Minneapolis, MN 55455-0431, USA
Publication date: January 1, 2015