Metal- and CO-Free Carbonylation of Alkyl Iodides

We report a new method for the carbonylation of alkyl iodides under photochemical conditions. The process relies on a simple aryl formate reagent, synthesized in one step from readily available chemicals and capable of releasing CO along with a phenolate species in the presence of a mild base. The photoactivity of this phenolate is harnessed to activate alkyl iodides via single-electron transfer and generate alkyl radicals that add to CO and ultimately offer access to carboxylic acids and amides. This new, user-friendly procedure overcomes the typical need for CO gas and/or metal catalysts in carbonylation chemistry while being highly efficient and versatile to accommodate a variety of functional groups.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-10-16
DOI
https://doi.org/10.1021/jacs.5c13505
Citations
1
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.70
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article

Metal- and CO-Free Carbonylation of Alkyl Iodides

Emilien Le Saux, Matthew Mathis, Bill Morandi, Giorgia Panizzolo
1 citations
Journal of the American Chemical Society
Carbon dioxide utilization in catalysis
0.70
article

Metal- and CO-Free Carbonylation of Alkyl Iodides

Emilien Le Saux, Matthew Mathis, Bill Morandi, Giorgia Panizzolo
article en
1 citations

Abstract

We report a new method for the carbonylation of alkyl iodides under photochemical conditions. The process relies on a simple aryl formate reagent, synthesized in one step from readily available chemicals and capable of releasing CO along with a phenolate species in the presence of a mild base. The photoactivity of this phenolate is harnessed to activate alkyl iodides via single-electron transfer and generate alkyl radicals that add to CO and ultimately offer access to carboxylic acids and amides. This new, user-friendly procedure overcomes the typical need for CO gas and/or metal catalysts in carbonylation chemistry while being highly efficient and versatile to accommodate a variety of functional groups.

Journal of the American Chemical SocietyVol. 147(43)
ETH Zurich (CH)
Openalex Percentile: Top 31%
Carbon dioxide utilization in catalysis
0.70
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