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Heterogenized Phenanthroline-Pd(2+)-Catalyzed Alkoxycarbonylation of Aryl Iodides in Base-Free Conditions

Authors
Ganesan, V.Moon, S.Yoon, Sungho
Issue Date
Apr-2023
Publisher
American Chemical Society
Citation
Journal of Organic Chemistry, v.88, no.8, pp 5127 - 5134
Pages
8
Journal Title
Journal of Organic Chemistry
Volume
88
Number
8
Start Page
5127
End Page
5134
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/67540
DOI
10.1021/acs.joc.2c02359
ISSN
0022-3263
1520-6904
Abstract
A phenanthroline-based porous organic polymer-supported heterogeneous Pd catalyst (Pd@Phen-POP) is facilely synthesized by the solvent knitting of a Phen scaffold via the Lewis-acid-catalyzed Friedel-Crafts reaction using dichloromethane as a source for linker in the presence of AlCl3. The catalyst very effectively catalyzes the alkoxycarbonylation of various substituted aryl iodides with various alcohols to give corresponding products in good to excellent yields. Owing to the heterotic nature of the catalyst, it can be easily separated by simple filtration from the reaction mixture and recycled. © 2023 American Chemical Society.
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