Direct arylation/alkylation/magnesiation of benzyl alcohols in the presence of Grignard reagents via Ni-, Fe-, or Co-catalyzed sp3 C-O bond activation

J Am Chem Soc. 2012 Sep 12;134(36):14638-41. doi: 10.1021/ja307045r. Epub 2012 Aug 28.

Abstract

Direct application of benzyl alcohols (or their magnesium salts) as electrophiles in various reactions with Grignard reagents has been developed via transition metal-catalyzed sp(3) C-O bond activation. Ni complex was found to be an efficient catalyst for the first direct cross coupling of benzyl alcohols with aryl/alkyl Grignard reagents, while Fe, Co, or Ni catalysts could promote the unprecedented conversion of benzyl alcohols to benzyl Grignard reagents in the presence of (n)hexylMgCl. These methods offer straightforward pathways to transform benzyl alcohols into a variety of functionalities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Benzyl Alcohols / chemistry*
  • Benzyl Compounds / chemical synthesis*
  • Benzyl Compounds / chemistry
  • Catalysis
  • Cobalt / chemistry
  • Indicators and Reagents
  • Iron / chemistry
  • Magnesium / chemistry*
  • Molecular Structure
  • Nickel / chemistry
  • Organometallic Compounds / chemical synthesis*
  • Organometallic Compounds / chemistry*

Substances

  • Benzyl Alcohols
  • Benzyl Compounds
  • Indicators and Reagents
  • Organometallic Compounds
  • Cobalt
  • Nickel
  • Iron
  • Magnesium