Synthesis of Benzo[c]acridine Derivatives: Reaction of N-Arylidenenaphthalen- 1-amine with 5,5-Dimethyl-1,3-cyclohexadione
Corresponding Author(s) : Gajanan B. Kasawar
kajanan2002@rediffmail.com
Asian Journal of Chemistry,
Vol. 20 No. 6 (2008): Vol 20 Issue 6
Abstract
Synthesis of 10,10-dimethyl-7-aryl-7,9,10,11-tetrahydro- 9H-benzo[c]acridin-8-one derivatives was accomplished in high yields via the reaction of N-arylidenenaphthalen-1-amine with 5,5-dimethyl-1,3-cyclohexadione in aqueous medium catalyzed by triethylbenzyl ammonium chloride. The structures were established from spectroscopic data and melting points.
Keywords
Synthesis
Benzo[c]acridine derivatives
Triethylbenzyl ammonium chloride
B. Kasawar, G., B. Shejul, P., H. Kadam, N., V. Vyavahare, A., & Panpaliya, P. (2010). Synthesis of Benzo[c]acridine Derivatives: Reaction of N-Arylidenenaphthalen- 1-amine with 5,5-Dimethyl-1,3-cyclohexadione. Asian Journal of Chemistry, 20(6), 4678–4684. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/19079
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