Related Experiment Video
Updated: Dec 24, 2025

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Copper-Promoted One-Pot Approach: Synthesis of Benzimidazoles
S N Murthy Boddapati1,2, Ramana Tamminana3, Ravi Kumar Gollapudi1
1Department of Chemistry, Acharya Nagarjuna University, Guntur, Andhar Pradesh 522510, India.
Abstract:
A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C-N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations revealed that the synthetic pathway involves a copper-based desulphurization/nucleophilic substitution and a subsequent domino intra and intermolecular C-N cross-coupling reactions. Some of the issues typically encountered during the synthesis of 2-arylaminobezimidazoles, including the use of expensive catalytic systems and the low reactivity of bromo precursors, were addressed using this newly developed copper-catalyzed method. The reaction procedure is simple, generally with excellent substrate tolerance, and provides good to high yields of the desired products.
Related Concept Videos
Nucleophilic Aromatic Substitution: Elimination–Addition
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Electrophilic Aromatic Substitution: Nitration of Benzene
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
