K2S2O8‐Promoted Haloamination of Non‐Functionalized Olefins for the Synthesis of 2‐Halomethyl Indolines and 2‐Halomethyl Dihydrobenzofuran

A metal‐free, economical and effective method for intramolecular haloamination/cyclization of non‐functionalized olefins was developed. In the presence of K2S2O8 and sodium halide, 2‐allyl aniline can be converted into corresponding 2‐iodo, bromo and chloromethyl indolines skeleton compounds in good...

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Veröffentlicht in:ChemistrySelect (Weinheim) 2022-09, Vol.7 (33), p.n/a
Hauptverfasser: Liu, Ruyan, Wang, Yan, Hu, Zhouman, Wu, Jianglong, Gong, Chengwei, Jiang, Zishuo, Li, Dianjun, Wang, Fuqiang, Yang, Jinhui
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Sprache:eng
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Zusammenfassung:A metal‐free, economical and effective method for intramolecular haloamination/cyclization of non‐functionalized olefins was developed. In the presence of K2S2O8 and sodium halide, 2‐allyl aniline can be converted into corresponding 2‐iodo, bromo and chloromethyl indolines skeleton compounds in good to excellent yields. Mechanism research suggested that the reaction didn't involve radical addition pathway. Introduction A metal‐free, economical and effective method for intramolecular haloamination of non‐functionalized olefins by K2S2O8 was introduced in detail. In the presence of K2S2O8 and Sodium halide, various non‐functionalized olefins can be converted into corresponding 2‐iodo, bromo and chloromethyl indolines skeleton compounds
ISSN:2365-6549
2365-6549
DOI:10.1002/slct.202201932