Facile intramolecular cyclization of N-(2 hydroxybenzoyl) hydrazones to N,N'-diacetyl benzo-1,3,4-oxadiazepine derivatives / Chan Pei Qie

Chan, Pei Qie (2018) Facile intramolecular cyclization of N-(2 hydroxybenzoyl) hydrazones to N,N'-diacetyl benzo-1,3,4-oxadiazepine derivatives / Chan Pei Qie. Masters thesis, University of Malaya.

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      Abstract

      The synthesis of seven-membered benzo-1,3,4-oxadiazepines can be carried out through one-step intramolecular cyclization of N-(2-hydroxybenzoyl)hydrazones. The reaction was catalyzed by 4.50% (v/v) of sulfuric acid in acetic anhydride (Vt = 1 mL) at room temperature. The catalytic and substituent effects on the reactivity of this intramolecular cyclization were investigated. Through this strategy, a series of benzo-1,3,4-oxadiazepine derivatives were prepared (with yield up to 83%). These new heterocyclic compounds were characterized through their melting point, NMR and HRMS (ESI). It was observed that when electron-withdrawing group is at the para position of salicylic ring and electron-donating group at the para position of benzylidene ring, a good yield of seven-membered benzoxadiazepines were obtained. This strategy provided good method to a variety of substitution.

      Item Type: Thesis (Masters)
      Additional Information: Dissertation (M.A.) – Faculty of Science, University of Malaya, 2018.
      Uncontrolled Keywords: Benzo-1,3,4-oxadiazepine; Brønsted acids; Cyclization; hydrazones; Substituent effects
      Subjects: Q Science > Q Science (General)
      Q Science > QD Chemistry
      Divisions: Faculty of Science
      Depositing User: Mr Mohd Safri Tahir
      Date Deposited: 08 Jul 2019 04:38
      Last Modified: 08 Jul 2019 04:39
      URI: http://studentsrepo.um.edu.my/id/eprint/9617

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