Naturally Occurring Organic Acid-catalyzed Facile Diastereoselective Synthesis of Biologically Active (E)-3-(arylimino)indolin-2-one Derivatives in Water at Room Temperature

Author(s): Gurpreet Kaur, Arvind Singh, Kiran Bala, Mamta Devi, Anjana Kumari, Sapna Devi, Rekha Devi, Vivek Kumar Gupta, Bubun Banerjee*.

Journal Name: Current Organic Chemistry

Volume 23 , Issue 16 , 2019

Become EABM
Become Reviewer

Graphical Abstract:


A simple, straightforward and efficient method has been developed for the synthesis of (E)-3-(arylimino)indolin-2-one derivatives and (E)-2-((4-methoxyphenyl)imino)- acenaphthylen-1(2H)-one. The synthesis of these biologically-significant scaffolds was achieved from the reactions of various substituted anilines and isatins or acenaphthaquinone, respectively, using commercially available, environmentally benign and naturally occurring organic acids such as mandelic acid or itaconic acid as catalyst in aqueous medium at room temperature. Mild reaction conditions, energy efficiency, good to excellent yields, environmentally benign conditions, easy isolation of products, no need of column chromatographic separation and the reusability of reaction media are some of the significant features of the present protocol.

Keywords: Aqueous medium, isatin based schiff base, itaconic acid, mandelic acid, organic acids as catalyst, room temperature reaction, sustainable synthesis.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2019
Page: [1778 - 1788]
Pages: 11
DOI: 10.2174/1385272822666190924182538
Price: $58

Article Metrics

PDF: 9