Abstract
7-Aryl-8 H -benzo[ f ]indeno[2,1- b ]quinoline-8-one derivatives were synthesized by means of a one-pot condensation of 2-naphthylamine, aromatic aldehydes, and indane-1,3-dione in ethanol under refluxing conditions in the presence of poly(4-vinylpyridinium) hydrogen sulfate, a solid acid catalyst. This method has the advantages of high yield, clean reaction, simple methodology, and short reaction time. The catalyst could be recycled and reused four times without significant loss of activity. The structure of the novel compounds was confirmed by IR, 1 H NMR, and 13 C NMR spectroscopy and elemental analysis. One-pot condensation of 2-naphthylamine, aromatic aldehydes, and indane-1,3-dione was performed in refluxing ethanol in the presence of poly(4-vinylpyridinium) hydrogen sulfate as a catalyst. The catalyst could be recycled and reused four times without significant loss of activity.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
