Robust continuous-flow synthesis of deuterium-labeled ¢-nitroalcohols catalyzed by basic anion exchange resin

Tsuyoshi Yamada, Kwihwan Park, Naoya Ito, Hayato Masuda, Wataru Teranishi, Sunliang Cui, Hironao Sajiki*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

A practical and efficient continuous-flow system was developed for the synthesis of site-selectively deuterium-labeled ¢- nitroalcohols by using the tertiary amine-functionalized basic anion exchange resin, WA30, as a heterogeneous organocatalyst. For this system, WA30 was prepacked in a cartridge under metal-free conditions. The system was operated by pumping a solution of aldehydes or ketones, as electrophiles, and nitroalkanes in a solvent system of deuterium oxide and THF in the catalyst cartridge. Various deuterated ¢-nitroalcohols were obtained in moderate to excellent yields with high deuteration efficiencies. The continuous-flow system was applied in continuous synthesis for at least 72 h without degradation of the heterogeneous organocatalyst activity.

Original languageEnglish
Pages (from-to)1000-1006
Number of pages7
JournalBulletin of the Chemical Society of Japan
Volume93
Issue number8
DOIs
StatePublished - 2020/08

Keywords

  • Continuous-flow reaction
  • Deuteration
  • Nitroaldol reaction

ASJC Scopus subject areas

  • General Chemistry

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