Water tolerant base free Copper (I) catalyst for the selective aerobic oxidation of primary alcohols

Emi Lagerspets, Donatella Abba, Joseph Sharratt, Aleksi Eronen, Timo Repo

Research output: Contribution to journalArticleScientificpeer-review

Abstract

We report here a base free copper(I) catalyst for the selective aerobic oxidation of primary alcohols to their corresponding aldehydes and various diols to their corresponding lactones or lactols. In the presence of the in situ generated Cu(I)-catalyst with 2,2′-dipyridylamine (dpa) as a ligand and 2,2,6,6-tetramethylpiperdine-N-oxyl (TEMPO) as a persistent radical, the oxidation reaction proceeds under true aerobic conditions, at ambient temperature, utilizing air as the oxidant and without added base. High catalytic activity without over oxidation was achieved for numerous primary alcohols (aliphatic, allylic, benzylic and diols) with different substitution patterns. The catalyst's stability is unique among reported Cu(I)-catalysts. It is not moisture or air sensitive, and is capable of e.g. oxidizing aliphatic and benzyl alcohols in a water/acetonitrile solution in moderate or in quantitative yield (> 99%) in 3 h.
Original languageEnglish
Article number112167
JournalMolecular catalysis
Volume520
Number of pages6
ISSN2468-8274
DOIs
Publication statusPublished - Mar 2022
MoE publication typeA1 Journal article-refereed

Fields of Science

  • ALDEHYDES
  • Aerobic oxidation
  • BENZYLIC ALCOHOLS
  • Base free
  • CHEMISTRY
  • CU(II) COMPLEXES
  • Catalyst
  • Copper(I)
  • EFFICIENT
  • LIGANDS
  • METAL
  • OXYGEN
  • SITE
  • SYSTEM
  • Water
  • acetonitrile mixture
  • 116 Chemical sciences

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