Nitration with ytterbium triflate catalyst

As anticipated from the complexation experiments, reaction of 4.42 with cyclopentadiene in the presence of copper(II)nitrate or ytterbium triflate was extremely slow and comparable to the rate of the reaction in the absence of Lewis-acid catalyst. Apparently, Lewis-acid catalysis of Diels-Alder reactions of p-amino ketone dienophiles is not practicable. 

Hafnium and zirconium mononitrate tris(triflate), [M(H20)x(N03)](0Tf)35 were prepared from their tetrachlorides in analogous fashion to the lanthanide salts. Much to our delight these (deliquescent) salts displayed A, nitrate stretching frequencies in their IR spectra at 1651 and 1650 cm1 respectively. Armed with this pleasing information and with a specific programme aim of nitrating o-nitrotoluene (ONT) to dinitrotoluenes (DNTs) with these catalyst types, (catalytic quantities of ytterbium(III) triflate were essentially ineffective for this transformation) hafnium(IV) and zirconium(IV) triflate were prepared as their hydrated salts via metathesis of their tetrachlorides with silver triflate in water. 

To avoid excessive acid waste, lanthanide(III) triflates are used as recyclable catalysts for economic aromatic nitration. Among a range of lanthanide(III) triflates examined, the ytterbium salt is the most effective. A catalytic quantity (1-10 mol%) of ytterbium(III) triflate catalyzes the nitration of simple aromatics with excellent conversions using an equivalent of 69% nitric acid in refluxing 1,2-dichloromethane for 12 h. The only by-product of the reaction is water, and the catalyst can be recovered by simple evaporation of the separated aqueous phase and reused repeatedly for further nitration.12... 

Ytterbium(III) Triflate as a Recyclable Catalyst for the Nitration of Arenes with Nitric Acid... 

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