Tuneable Copper Catalysed Transfer Hydrogenation of Nitrobenzenes to Aniline or Azo Derivatives. Issue 13 (11th May 2020)

• Record Type: Journal Article
• Authors: Moran, Maria Jesus; Martina, Katia; Baricco, Francesca; Tagliapietra, Silvia; Manzoli, Maela; Cravotto, Giancarlo
• Is Part Of: Advanced synthesis & catalysis. Volume 362:Issue 13(2020)
• Page Start: 2689
• Page End: 2700
• Publication Date: 2020-05-11
• Subjects: copper nanoparticles -- azoarene -- nitrobenzene -- microwaves -- ultrasound; Catalysis -- Periodicals; Organic compounds -- Synthesis -- Periodicals; Chemistry -- Periodicals; Chemistry, Technical -- Periodicals; Chemistry -- Periodicals; Catalysis -- Periodicals; Technology, Pharmaceutical -- Periodicals; 547.2
• DOI: 10.1002/adsc.202000127
• Languages: English
• ISSNs: 1615-4150

Abstract

Abstract: A highly versatile and flexible copper nanoparticle (Cu(0) NPs) catalytic system has been developed for the controlled and selective transfer hydrogenation of nitroarene. Interestingly, the final catalytic product is strongly dependent on the nature of the hydrogen donor source. The yield of nitrobenzene reduction to aniline increased from 20% to an almost quantitative yield over a range of alcohols, diols and aminoalcohols. In glycerol at 130 °C aniline was isolated in 93% yield. In ethanolamine, the reaction was conveniently performed at a lower temperature (55 °C) and gave selectively substituted azobenzene (92% yield). Experimental studies provide support for a reaction pathway in which the Cu(0) NPs catalysed transfer hydrogenation of nitrobenzene to aniline proceeds via the condensation route. The high chemoselectivity of both protocols has been proved in experiments on a panel of variously substituted nitroarenes. Enabling technologies, microwaves and ultrasound, used both separately and in combination, have successfully increased the reaction rate and reaction yield. Abstract :