International Journal of Chemical Studies
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P-ISSN: 2349-8528, E-ISSN: 2321-4902   |   Impact Factor: GIF: 0.565 NAAS Rating: 5.31 NEW

International Journal of Chemical Studies

Vol. 5, Issue 1 (2017)
Synthesis and Characterisation of substituted Quinoline by Vilsmeier-Haack reagent


Author(s): Tekale AS and Shaikh SAL

Abstract: For the synthesis of substituted i.e. 2-chloro-3-formyl-8-methyl Quinoline an highly efficient, simple and convenient method through Vilsmeier-Haack reagent has been developed in high yields, less raw material, and less time requiring for completion of reaction. In the present research work the substituted quinoline and acetanilide are synthesized through Vilsmeier reaction has been reported to the substitution reaction by substituted acetanilide bearing electron donating group at ortho position and electron attracting group at ortho position are investigated and it is good in all case. Further, the nucleophilic substitution reaction of the substituted quinoline is also investigated. Similarly in quinoline the –CHO (formyl) group is subjected for further transformation of formyl group in to (4’-NO2 nitro group, 3’N-NH-C6H5) 3’-CH3 group and 3’-N-benzylidene group.

Pages: 01-04  |  1548 Views  159 Downloads

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How to cite this article:
Tekale AS, Shaikh SAL. Synthesis and Characterisation of substituted Quinoline by Vilsmeier-Haack reagent. Int J Chem Stud 2017;5(1):01-04.
International Journal of Chemical Studies