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A mild one-pot transformation of nitroalkanes to ketones or aldehydes via a visible-light photocatalysis-hydrolysis sequence.

Yin-Yin HsuSheng-Qi LuoBor-Cherng HongSu-Ying Chien
Published in: Organic & biomolecular chemistry (2022)
Using a visible-light photoredox catalysis strategy with household decorative blue LEDs and the additives Et 3 N and DIPEA, as well as the subsequent hydrolysis sequence, a mild one-pot process for the direct transformation of nitroalkanes to the corresponding ketones and aldehydes, constituting a Nef-like reaction, has been developed. It is worth noting that by using an appropriate photocatalyst ( e.g. , [Ir(dtbbpy)(ppy) 2 ]PF 6 ) and the extra additive Et 3 N with the combination of DIPEA and Mg(ClO 4 ) 2 in i-PrOH (instead of CH 3 CN), the transformation of nitroalkanes to the corresponding oximes, rather than nitrones, can be markedly more effective. The oximes can then be hydrolyzed to ketones by reaction with CuCl 2 ·2H 2 O in a pH 7 buffer solution. This process is appealing because of the benefits of efficient conversion, mild conditions, high yields, and general applicability to compounds with a wide range of labile functional groups.
Keyphrases
  • visible light
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  • room temperature
  • electron transfer