Nickel‐Catalyzed Cyanoalkylation of Ketone Derivatives

Author:

Coffinet Anaïs1,Levacher Vincent1,Gillaizeau Isabelle2ORCID,Brière Jean‐François1ORCID,Oudeyer Sylvain1ORCID

Affiliation:

1. Normandie Univ, UNIROUEN INSA Rouen, CNRS, COBRA 76000 Rouen France

2. Université d'Orléans, CNRS, ICOA UMR 7311 Orléans 45067 France

Abstract

AbstractAlthough the metal‐based catalyzed cyanomethylation of aldehydes is well‐developed, a similar approach to ketones with acetonitrile derivatives remains a challenge. Thanks to Tolman type complexes, NiII‐complexes with a pyridine(dicarboxamide) pincer ligand, an alternative metal‐catalyzed (1–5 mol% catalyst) cyanomethylation of an array of isatins and activated ketones is reported at room temperature. High isolated yields (up to 99%) were obtained not only with the poorly acidic acetonitrile but also with more challenging substituted alkyl cyanide nucleophiles. The in situ generated putative ion paired catalysts [NiCR2CN]Cat+ likely benefit from the cation part (Cs+ or n‐Bu4N+) to facilitate their formation and catalytic activity.magnified image

Funder

Région Normandie

Publisher

Wiley

Subject

General Chemistry

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