EconPapers    
Economics at your fingertips  
 

Synthesis of a Number of Unsymmetrical Bridged Terphthaloyl Acetophenone Oxime Esters

Ramadan Ali Bawa and Hana Mansoure Elmajdoub
Additional contact information
Ramadan Ali Bawa: Chemistry Department, Faculty of Science, Misurata University, Misurata, Libya
Hana Mansoure Elmajdoub: Chemistry Department, Faculty of Science, Misurata University, Misurata, Libya

Academic Journal of Chemistry, 2020, vol. 5, issue 7, 98-100

Abstract: A number of unsymmetrical bridged terphthaloyl acetophenone oxime esters has been synthesized throughout an esterification reaction between four different acetophenone oximes and the terphthaloyl chloride in a molar ratio of (2:1) under mild basic conditions. Spectroscopic techniques, such as IR, HNMR and mass spectrometer, were used to confirm the structures of the targeted oxime esters. The yields of the obtained oxime esters ranged from 80% to 95%.

Keywords: Unsymmetrical; Bridged; Oxime esters; Esterification; Spectroscopic (search for similar items in EconPapers)
Date: 2020
References: Add references at CitEc
Citations:

Downloads: (external link)
https://www.arpgweb.com/pdf-files/ajc5(7)98-100.pdf (application/pdf)
https://www.arpgweb.com/journal/20/archive/09-2020/7/5 (text/html)

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:arp:ajcarp:2020:p:98-100

DOI: 10.32861/ajc.57.98.100

Access Statistics for this article

Academic Journal of Chemistry is currently edited by Prof. Dr. Sadek khalifa Shakshooki

More articles in Academic Journal of Chemistry from Academic Research Publishing Group Rahim Yar Khan 64200, Punjab, Pakistan.
Bibliographic data for series maintained by Managing Editor ().

 
Page updated 2025-03-19
Handle: RePEc:arp:ajcarp:2020:p:98-100