Direct synthesis of 2,3-dihydroperimidine derivatives <i>via</i> dehydrogenative C–N coupling using a recyclable Fe catalyst

We report here an efficient and sustainable protocol for the direct synthesis of 2,3-dihydroperimidine derivatives <i>via</i> dehydrogenative C-N coupling, utilizing a recyclable Fe single-atom catalyst supported on nitrogen-doped carbon (Fe<sub>1</sub>-N-C). The catalyst was synthesized by encapsulating ferrocene within the ZIF-8 framework, followed by pyrolysis. The catalyst exhibited excellent activity, stability, and recyclability, facilitating the transformation of diverse primary alcohols, including aryl/heteroaryl methanol and aliphatic alcohols, into the desired products in moderate to good yields. To delineate the mechanism, several control experiments were performed, revealing the formation of aldehyde as the intermediate, which subsequently underwent annulation with naphthalene-1,8-diamine. Additionally, the gram-scale synthesis further showcased the versatility of the catalyst as well as the protocol.

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Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob01009h
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Direct synthesis of 2,3-dihydroperimidine derivatives via dehydrogenative C–N coupling using a recyclable Fe catalyst

Sandra Shabu
Organic & Biomolecular Chemistry
Asymmetric Hydrogenation and Catalysis
article

Direct synthesis of 2,3-dihydroperimidine derivatives via dehydrogenative C–N coupling using a recyclable Fe catalyst

Sandra Shabu
article en

Abstract

We report here an efficient and sustainable protocol for the direct synthesis of 2,3-dihydroperimidine derivatives <i>via</i> dehydrogenative C-N coupling, utilizing a recyclable Fe single-atom catalyst supported on nitrogen-doped carbon (Fe<sub>1</sub>-N-C). The catalyst was synthesized by encapsulating ferrocene within the ZIF-8 framework, followed by pyrolysis. The catalyst exhibited excellent activity, stability, and recyclability, facilitating the transformation of diverse primary alcohols, including aryl/heteroaryl methanol and aliphatic alcohols, into the desired products in moderate to good yields. To delineate the mechanism, several control experiments were performed, revealing the formation of aldehyde as the intermediate, which subsequently underwent annulation with naphthalene-1,8-diamine. Additionally, the gram-scale synthesis further showcased the versatility of the catalyst as well as the protocol.

Organic & Biomolecular ChemistryVol. 23(39)
National Institute of Technology Calicut (IN)
Department of Science and Technology, Ministry of Science and Technology, India, National Institute of Technology Calicut
Openalex Percentile: Top 82%
Asymmetric Hydrogenation and Catalysis
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