1. Home
    2. Journals
    3. Journal of Chemical Sciences
    4. Volume 89
    5. Issue 3

    • Fulltext

       

        Click here to view fulltext PDF


      Permanent link:
      https://www.ias.ac.in/article/fulltext/jcsc/089/03/0295-0299

    • Keywords

       

      Isothiocyanates; a-anilino benzylnitrile; thin layer chromatography; thiazolines

    • Abstract

       

      Interaction of aryl/alkyl isothiocyanates and a-anilino benzylnitrile has been found to afford the corresponding 5-amino-4-phenyl-3-aryl-2-aryl/alkylimino thiazolines. These have been characterised. The reaction is found to be a general one. The thiazolines on hydrolysis with alkali afford hydrogen sulphide, benzaldehyde along with nonreacted products. Formation of these products, obtained by the hydrolysis, has been confirmed by thin layer chromatography.

    • Author Affiliations

       

      S T Ingle1 S M Kapley1 M S Chande1

      1. Department of Chemistry, Institute of Science, Nagpur - 440 001, India

    • Dates

       
      Published
      June 1980
      Manuscript received
      26 November 1979
      Manuscript revised
      1 February 1980

  • Journal of Chemical Sciences | News

© 2022-2023 Indian Academy of Sciences, Bengaluru.

Contact | Site index