Catalyst, Base, Additives, and Solvent: The Tools to Dig a Better CANAL Reaction

The Catalytic Arene Norbornene Annulation (CANAL) reaction has been established as an effective method for the preparation of norbornene-cyclobutenyl-arene products. To expand the scope of this reaction to encompass sensitive substrates, such as ones which will provide next generation polyacene dimers, we herein report the development of a CANAL protocol through a parallel experimentation approach, aiming to reduce the temperature of the reaction. This was accomplished through exploration and modification of the catalyst-ligand system, base, solvent, and concerted metalation-deprotonation (CMD) promoters, providing conditions with typical temperatures of 70 °C and as low as 60 °C with some substrates. Through these studies, we have discovered reliable conditions for aryl bromides, chlorides, and triflates. In addition, we have demonstrated the utility of these conditions through preparation of a novel anthracene dimer, TIPS-BAS, which could not be prepared using literature conditions.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-08-08
DOI
https://doi.org/10.1021/acs.joc.5c01281
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Catalyst, Base, Additives, and Solvent: The Tools to Dig a Better CANAL Reaction

Tarek Sammakia, Kajal Kajal, Ethan G. Miller, Niels H. Damrauer
1 links
The Journal of Organic Chemistry
Asymmetric Hydrogenation and Catalysis
article

Catalyst, Base, Additives, and Solvent: The Tools to Dig a Better CANAL Reaction

Tarek Sammakia, Kajal Kajal, Ethan G. Miller, Niels H. Damrauer
article en

Abstract

The Catalytic Arene Norbornene Annulation (CANAL) reaction has been established as an effective method for the preparation of norbornene-cyclobutenyl-arene products. To expand the scope of this reaction to encompass sensitive substrates, such as ones which will provide next generation polyacene dimers, we herein report the development of a CANAL protocol through a parallel experimentation approach, aiming to reduce the temperature of the reaction. This was accomplished through exploration and modification of the catalyst-ligand system, base, solvent, and concerted metalation-deprotonation (CMD) promoters, providing conditions with typical temperatures of 70 °C and as low as 60 °C with some substrates. Through these studies, we have discovered reliable conditions for aryl bromides, chlorides, and triflates. In addition, we have demonstrated the utility of these conditions through preparation of a novel anthracene dimer, TIPS-BAS, which could not be prepared using literature conditions.

The Journal of Organic ChemistryVol. 90(33)
Energy Institute (GB), University of Colorado Boulder (US), University of Colorado System (US)
University of Colorado Boulder, Division of Chemistry
Clean water and sanitation
Openalex Percentile: Top 84%
Asymmetric Hydrogenation and Catalysis
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