Misplaced Pages

Cadiot–Chodkiewicz coupling

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
(Redirected from Cadiot-Chodkiewicz coupling) Reaction in organic chemistry

Cadiot–Chodkiewicz coupling
Named after Paul Cadiot
Wladyslaw Chodkiewicz
Reaction type Coupling reaction
Identifiers
Organic Chemistry Portal cadiot-chodkiewicz-coupling
RSC ontology ID RXNO:0000100

The Cadiot–Chodkiewicz coupling in organic chemistry is a coupling reaction between a terminal alkyne and a haloalkyne catalyzed by a copper(I) salt such as copper(I) bromide and an amine base. The reaction product is a 1,3-diyne or di-alkyne.

The reaction mechanism involves deprotonation by base of the terminal alkyne proton followed by formation of a copper(I) acetylide. A cycle of oxidative addition and reductive elimination on the copper centre then creates a new carbon-carbon bond.

Scope

Unlike the related Glaser coupling the Cadiot–Chodkiewicz coupling proceeds selectively and will only couple the alkyne to the haloalkyne, giving a single product. By comparison the Glaser coupling would simply produce a distribution of all possible couplings. In one study the Cadiot–Chodkiewicz coupling has been applied in the synthesis of acetylene macrocycles starting from cis-1,4-diethynyl-1,4-dimethoxycyclohexa-2,5-diene. This compound is also the starting material for the dibromide through N-bromosuccinimide (NBS) and silver nitrate:

Cadiot–Chodkiewicz coupling application
Cadiot–Chodkiewicz coupling application

The coupling reaction itself takes place in methanol with piperidine, the hydrochloric acid salt of hydroxylamine and copper(I) bromide.

See also

References

  1. Chodkiewicz, W. Ann. Chim. Paris 1957, 2, 819–69.
  2. Cadiot, P.; Chodkiewicz, W. In Chemistry of Acetylenes; Viehe, H. G., Ed.; Marcel Dekker: New York, 1969; pp. 597–647.
  3. ^ Bandyopadhyay, Arkasish; Varghese, Babu; Sankararaman, Sethuraman (2006). "Synthesis of 1,4-Cyclohexadiene-Based Acetylenic Macrocycles with Cadiot–Chodkiewicz Coupling. Structure of a Tub-Shaped Tetrameric Container". Journal of Organic Chemistry. 71 (12): 4544–4548. doi:10.1021/jo0605290. PMID 16749787.
Alkynes
Preparations
Reactions
Topics in organic reactions
List of organic reactions
Carbon-carbon
bond forming
reactions
Homologation reactions
Olefination reactions
Carbon-heteroatom
bond forming
reactions
Degradation
reactions
Organic redox
reactions
Rearrangement
reactions
Ring forming
reactions
Cycloaddition
Heterocycle forming reactions
Categories: