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.
Authors
- Makoto Onaka (ORCID: https://orcid.org/0000-0001-7893-7264)
- Shintaro Shibata (ORCID: https://orcid.org/0009-0004-7057-7099)
Institutions
- Tokyo University of Agriculture (JP)
- Research Foundation ITSUU Laboratory (JP)
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
Funders
- Keio University
- University of Tokyo
- Kanagawa University
- Tokyo University of Agriculture