Synthesis of <i>N</i>‑Bromo and <i>N</i>‑Iodo Imides: A Rapid Redox-Neutral and Bench Stable\nProcess

This report presents\na rapid, ecofriendly technique for the formation\nof commonly used <i>N</i>-bromo and <i>N</i>-iodinating\nreagents by reacting readily available <i>N</i>-chloro derivatives\nwith inorganic bromide and iodide salts. All reagents were easily\nhandled, commercially available, and bench stable. This strategy illustrates\nthe expeditious formation of these halogenating reagents in multigram\nscale in high-yields and purity with an operationally straightforward\nrecrystallization. The mechanistic details suggest an in situ generation\nof an interhalogen species.

Publication Details

Journal
Figshare
Published
2024-10-11
DOI
https://doi.org/10.1021/acs.oprd.4c00194.s001
Primary Topic
Plant Taxonomy and Phylogenetics
Type
article
Field-Weighted Citation Impact
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article

Synthesis of N‑Bromo and N‑Iodo Imides: A Rapid Redox-Neutral and Bench Stable\nProcess

Figshare
Plant Taxonomy and Phylogenetics
article

Synthesis of N‑Bromo and N‑Iodo Imides: A Rapid Redox-Neutral and Bench Stable\nProcess

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Abstract

This report presents\na rapid, ecofriendly technique for the formation\nof commonly used <i>N</i>-bromo and <i>N</i>-iodinating\nreagents by reacting readily available <i>N</i>-chloro derivatives\nwith inorganic bromide and iodide salts. All reagents were easily\nhandled, commercially available, and bench stable. This strategy illustrates\nthe expeditious formation of these halogenating reagents in multigram\nscale in high-yields and purity with an operationally straightforward\nrecrystallization. The mechanistic details suggest an in situ generation\nof an interhalogen species.

Figshare
Openalex Percentile: Top 45%
Plant Taxonomy and Phylogenetics
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Synthesis of <i>N</i>‑Bromo and <i>N</i>‑Iodo Imides: A Rapid Redox-Neutral and Bench Stable\nProcess · Figshare (2024) | TGRS Research Map | TGRS