Sustainable purification-free synthesis of N–H ketimines by solid acid catalysis

Among imines, nitrogen-unprotected ketimines (N-H ketimines) are valuable precursors to nitrogen-containing compounds. However, their applications are limited compared with those of nitrogen-protected ketimines (N-R ketimines) owing to difficulties in synthesis and purification. We develop remarkably simple methods for synthesizing and isolating high-purity N-H ketimines and N-H ketimine hydrochlorides via the dehydration-condensation of ketones with stoichiometric ammonia, generated in situ with inorganic solid acid catalysts. Our methods offer exceptionally broad substrate scope, use non-toxic and reusable catalysts, do not require tedious synthetic steps, are inexpensive, and are suited to large-scale production. Additionally, ketones can be easily converted to N-R ketimines, α-aminonitriles, and hydantoins in one pot via N-H ketimines. All products can be isolated by filtration or concentration; other purification methods, such as column chromatography, are not required. This study guides the advancement of the design of new transition metal catalysts and pharmaceutical synthesis.

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Publication Details

Journal
Nature Communications
Published
2025-12-10
DOI
https://doi.org/10.1038/s41467-025-66949-5
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94

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article

Sustainable purification-free synthesis of N–H ketimines by solid acid catalysis

Makoto Onaka, Shintaro Shibata
1 citations
Nature Communications
Catalytic C–H Functionalization Methods
0.94
article

Sustainable purification-free synthesis of N–H ketimines by solid acid catalysis

Makoto Onaka, Shintaro Shibata
article en
1 citations

Abstract

Among imines, nitrogen-unprotected ketimines (N-H ketimines) are valuable precursors to nitrogen-containing compounds. However, their applications are limited compared with those of nitrogen-protected ketimines (N-R ketimines) owing to difficulties in synthesis and purification. We develop remarkably simple methods for synthesizing and isolating high-purity N-H ketimines and N-H ketimine hydrochlorides via the dehydration-condensation of ketones with stoichiometric ammonia, generated in situ with inorganic solid acid catalysts. Our methods offer exceptionally broad substrate scope, use non-toxic and reusable catalysts, do not require tedious synthetic steps, are inexpensive, and are suited to large-scale production. Additionally, ketones can be easily converted to N-R ketimines, α-aminonitriles, and hydantoins in one pot via N-H ketimines. All products can be isolated by filtration or concentration; other purification methods, such as column chromatography, are not required. This study guides the advancement of the design of new transition metal catalysts and pharmaceutical synthesis.

Nature CommunicationsVol. 16(1)
Tokyo University of Agriculture (JP), Research Foundation ITSUU Laboratory (JP)
Keio University, University of Tokyo, Kanagawa University, Tokyo University of Agriculture
Openalex Percentile: Top 19%
Catalytic C–H Functionalization Methods
0.94
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