The crystal structure of a novel product from the acid-catalyzed condensation of 1-benzylindole with acetone

Wayland E Noland, Michael J. Konkel, Susan J. Fanburg, Shankar Venkatraman, Doyle Britton

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

The acid-catalyzed condensation of 1-benzylindole with acetone in the presence of N-phenylmaleimide gave a tetrahydrocarbazole, (4,5,10,10b-tetrahydro-5-methyl-2-phenyl-10-(phenylmethyl)pyrrolo[3,4-a]carbazol e-1,3[2H, 3aH]-dione (1), as the major product and a novel spiro compound, 1′,3,4,4′-tetrahydro-1′,1′,3,3-tetramethyl-4,4′-bi s(phenylmethyl)-1,3′(2H, 2′H)-spiro[cyclopent[b]indole] (2), as the minor product. The structure of the spiro compound was determined by an X-ray crystallographic determination. The acid-catalyzed condensation of 1-benzylindole with acetone in the absence of N-phenylmaleimide gave a bisindole, (1,1′-bis(phenylmethyl)-3,3′-(1-methylethylidene)diindole (3), as the major product and the spiro-compound as the minor product.

Original languageEnglish (US)
Pages (from-to)9-14
Number of pages6
JournalJournal of Chemical Crystallography
Volume29
Issue number1
DOIs
StatePublished - Jan 1999

Keywords

  • 1-benzylindole
  • Acetone
  • Spiro[cyclopent[b]indole]

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