4.5 Article

Consecutive One-Pot Sonogashira-Glaser Coupling Sequence - Direct Preparation of Symmetrical Diynes by Sequential Pd/Cu Catalysis

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2011, Issue 2, Pages 238-242

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201001472

Keywords

Alkynes; C-C coupling; Copper; Multicomponent reactions; Palladium

Funding

  1. Merck Serono KGaA, Darmstadt

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Sonogashira coupling and the catalytic Glaser coupling are both catalyzed by the Pd-Cu complex couple and can be concatenated to a consecutive sequentially Pd/Cu-catalyzed process in a one-pot fashion, and air oxygen serves as the only oxidant in the second step. In a pseudo-four-component synthesis, a broad variety of symmetrically substituted 1,4-bis(hetero)aryl-1,3-butadiynes are obtained in good to excellent yields. Interestingly, the presence of iodide ions has been found to be advantageous over other halides to trigger the Pd/Cu-catalyzed Glaser step, and Pd and Cu species, as well as triethylamine as a base, are prerequisite for both couplings, which proceed with higher efficiency if performed in a one-pot sequence.

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