Sustainable Pd‐Catalyzed Aminations “on <i>Dirty</i> Water”

A new approach to Pd-catalyzed C─N bond formation is disclosed based on observations from Nature, where its use of an "on water" phenomenon allows for variations in its pH and content. By employing highly basic conditions generated from addition of a certain amount of KOH (i.e., the "dirt") to the water, aminations take place quickly. This "on dirty water" approach also provides the needed base, further simplifying reactions. The viscosity of the KOH/water (i.e., 30% KOH) presumably prevents dissolution of the organic coupling partners; hence, base-sensitive groups (e.g., esters, nitriles, etc.) are readily accommodated, thereby broadening the scope of this process. Recycling of this highly basic medium is also illustrated, resulting in a very low complete E-Factor. Several comparisons with recent literature routes are made using not only Pd catalysis, but also with aminations based on earth-abundant metals such as Ni and Cu, which tend to be carried out in various organic solvents. Water-based sequences are also shown, including chemoenzymatic catalysis. Prospects for extending this discovery to several other types of valuable bond formations in synthetic chemistry are also presented.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-06-26
DOI
https://doi.org/10.1002/anie.9297515
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Sustainable Pd‐Catalyzed Aminations “on Dirty Water”

Erfan Oftadeh, Bruce H. Lipshutz, Jie Yang, Marco Ortiz et al.
Angewandte Chemie International Edition
Catalytic Cross-Coupling Reactions
article

Sustainable Pd‐Catalyzed Aminations “on Dirty Water”

Erfan Oftadeh, Bruce H. Lipshutz, Jie Yang, Marco Ortiz, Kylee Dismuke Rodriguez
article en

Abstract

A new approach to Pd-catalyzed C─N bond formation is disclosed based on observations from Nature, where its use of an "on water" phenomenon allows for variations in its pH and content. By employing highly basic conditions generated from addition of a certain amount of KOH (i.e., the "dirt") to the water, aminations take place quickly. This "on dirty water" approach also provides the needed base, further simplifying reactions. The viscosity of the KOH/water (i.e., 30% KOH) presumably prevents dissolution of the organic coupling partners; hence, base-sensitive groups (e.g., esters, nitriles, etc.) are readily accommodated, thereby broadening the scope of this process. Recycling of this highly basic medium is also illustrated, resulting in a very low complete E-Factor. Several comparisons with recent literature routes are made using not only Pd catalysis, but also with aminations based on earth-abundant metals such as Ni and Cu, which tend to be carried out in various organic solvents. Water-based sequences are also shown, including chemoenzymatic catalysis. Prospects for extending this discovery to several other types of valuable bond formations in synthetic chemistry are also presented.

Angewandte Chemie International Edition
University of California, Santa Barbara (US)
National Science Foundation
Responsible consumption and production
Openalex Percentile: Top 12%
Catalytic Cross-Coupling Reactions
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Sustainable Pd‐Catalyzed Aminations “on <i>Dirty</i> Water” — Erfan Oftadeh, Bruce H. Lipshutz, et al. · Angewandte Chemie International Edition (2026) | TGRS Research Map | TGRS