Scalable and safe synthetic organic electroreduction inspired by Li-ion battery chemistry

  • Byron K. Peters
  • , Kevin X. Rodriguez
  • , Solomon H. Reisberg
  • , Sebastian B. Beil
  • , David P. Hickey
  • , Yu Kawamata
  • , Michael Collins
  • , Jeremy Starr
  • , Longrui Chen
  • , Sagar Udyavara
  • , Kevin Klunder
  • , Timothy J. Gorey
  • , Scott L. Anderson
  • , Matthew Neurock
  • , Shelley D. Minteer
  • , Phil S. Baran*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

356 Citations (Scopus)

Abstract

Reductive electrosynthesis has faced long-standing challenges in applications to complex organic substrates at scale. Here, we show how decades of research in lithium-ion battery materials, electrolytes, and additives can serve as an inspiration for achieving practically scalable reductive electrosynthetic conditions for the Birch reduction. Specifically, we demonstrate that using a sacrificial anode material (magnesium or aluminum), combined with a cheap, nontoxic, and water-soluble proton source (dimethylurea), and an overcharge protectant inspired by battery technology [tris(pyrrolidino)phosphoramide] can allow for multigram-scale synthesis of pharmaceutically relevant building blocks. We show how these conditions have a very high level of functional-group tolerance relative to classical electrochemical and chemical dissolving-metal reductions. Finally, we demonstrate that the same electrochemical conditions can be applied to other dissolving metal-type reductive transformations, including McMurry couplings, reductive ketone deoxygenations, and epoxide openings.

Original languageEnglish
Pages (from-to)838-845
Number of pages8
JournalScience
Volume363
Issue number6429
DOIs
Publication statusPublished - 2019
Externally publishedYes

Fingerprint

Dive into the research topics of 'Scalable and safe synthetic organic electroreduction inspired by Li-ion battery chemistry'. Together they form a unique fingerprint.

Cite this