CoBr2-catalyzed straightforward synthesis of quinoxalines via dehydrogenative coupling strategy

TitleCoBr2-catalyzed straightforward synthesis of quinoxalines via dehydrogenative coupling strategy
Publication TypeJournal Article
Year of Publication2025
AuthorsDubey, S, Punji, B
JournalChemistry-an Asian Journal
Volume20
Issue24
Date PublishedDEC
Type of ArticleArticle
ISSN1861-4728
Keywordscobalt, dehydrogenative coupling, heterocycles, ligand-free process, Quinoxaline
Abstract

Establishing a benign and straightforward protocol for synthesizing biorelevant and synthetically valuable quinoxaline is very important. Herein, we report a simple and efficient protocol for the sustainable synthesis of diverse quinoxaline derivatives catalyzed by cobalt salt. The reaction proceeds through the dehydrogenative coupling of alkyl and aryl ethane 1,2-diols with aryl diamines in the presence of a catalytic CoBr2/K2CO3. The usage of the greener solvent 2-MeTHF and the release of H2 and H2O as the sole byproducts make the process advantageous. The protocol led to the synthesis of diverse quinoxalines bearing synthetically useful functionalities, such as fluoro, chloro, bromo, cyano, trifluoromethyl, and ether. The reaction is presumed to proceed via the dehydrogenative-condensation pathway involving a cobalt-hydride intermediate.

DOI10.1002/asia.202500916
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

3.3

Divison category: 
Organic Chemistry
Database: 
Web of Science (WoS)

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