Related Experiment Video
Updated: Mar 28, 2026
![[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)
[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
C-H bond halogenation catalyzed or mediated by copper: an overview
1Key Laboratory of the Functional Small Organic Molecules, Ministry of Education, and College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P.R. China.
This review covers advances in copper-catalyzed carbon-halogen (C-X) bond formation using direct C-H activation. It highlights methods for synthesizing C-F, C-Cl, C-Br, and C-I bonds, crucial in organic synthesis.
Area of Science:
- Organic Chemistry
- Catalysis
- Synthetic Methodology
Background:
- Carbon-halogen (C-X) bonds are fundamental in organic synthesis.
- Their formation is critical for creating diverse organic molecules.
- Direct C-H functionalization offers a more efficient synthetic route.
Purpose of the Study:
- To review recent advancements in copper-catalyzed C-X bond formation.
- To focus on methods utilizing direct C-H bond transformation.
- To cover the synthesis of various C-X bonds (X = F, Cl, Br, I).
Main Methods:
- Copper-catalyzed reactions
- Direct C-H activation strategies
- Halogenation reactions
Main Results:
- Successful copper-catalyzed direct C-H halogenation methods have been developed.
- These methods enable the formation of C-F, C-Cl, C-Br, and C-I bonds.
- The review consolidates key strategies and catalytic systems.
Conclusions:
- Copper catalysis provides effective pathways for direct C-H halogenation.
- These methods offer significant advantages in organic synthesis.
- Further development in this area holds great promise for efficient molecule construction.
More Related Videos
06:34Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides CHIPS
Published on: June 20, 2014
09:35Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Related Concept Videos
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Base-Promoted α-Halogenation of Aldehydes and Ketones
Acid-Catalyzed α-Halogenation of Aldehydes and Ketones
In the first step of the mechanism, the acid protonates the carbonyl oxygen resulting in a resonance-stabilized cation, which subsequently loses an α-hydrogen to form an enol tautomer. The C=C bond in an enol is highly nucleophilic because of the electron-donating nature of the –OH group. Consequently, the double bond attacks an electrophilic halogen to form a...
Electrophilic Addition to Alkynes: Hydrohalogenation
Reactions at the Benzylic Position: Halogenation
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene