122422-38-2Relevant academic research and scientific papers
Interaction of 3,5-di-tert-butyl-o-benzoquinone with secondary amines - A pathway to new sterically hindered N,N-disubstituted o-aminophenols
Cherkasov, Vladimir,Druzhkov, Nikolay,Kocherova, Tatiana,Fukin, Georgii,Shavyrin, Andrey
experimental part, p. 80 - 84 (2011/02/28)
The interaction of 3,5-di-tert-butyl-o-benzoquinone with secondary amines has been studied. The synthetic procedure was developed in order to synthesize a series of new N,N-disubstituted o-aminophenols. The interaction of 3,5-di-tert-butyl-o-benzoquinone
Reaction de derives a liaison germanium-azote (germylamines, cyclogermazanes et germa-imines transitoires) avec la di-t-butyl-3,5-orthoquinone
Riviere-Baudet, M.,Riviere, P.,Khallaayoun, A.,Satge, J.,Rauzy, K.
, p. 77 - 94 (2007/10/02)
Several germanium-nitrogen compounds were treated with 3,5-di-t-butylorthoquinone (1).In the case of germylamines R3GeNMe2 (R = Et, Ph), 1,2 and 1,4 adducts were formed, as shown by 1H NMR spectroscopy.The thermally unstable 1,4 adduct, decomposes with nitrene elimination to give 2,2-dialkyl or 2,2-diaryl (6,8-di-t-butyl)-4,5-benzo-2-germa-1,3-dioxolane.The 1,2 adduct, through intermolecular redistribution, leads to digermyloxide (R3Ge)2O and a gem-diamine with partial regeneration of the starting quinone 1.These addition reactions proceed through a monoelectric transfer mechanism, with formation of a transient o-semiquinonic radical identified by ESR spectroscopy.This transient radical leads to O-germyl 3,5-di-t-butylcatechol by hydrogen abstraction from the solvent.The proposed mechanism explains the formation of the germylated compounds as well as the organic by-products.Similar reactions were observed between cyclodigermazanes and 1.The 1,4 cycloaddition generates germadioxolanes with nitrene expulsion, whereas the 1,2-cycloaddition leads to the germoxane and conjugated ketoimine, or diimine.The latter is a good trapping agent for the nitrene formed in the decomposition of the 1,4 adduct.Both the 1,4 and 1,2 cycloadduct decompositions imply transient germaimine formation.The same germaimine, formed at room temperature from intramolecular dehydrogenation of the hindered R2ClGeNHR' by 1,8-diazabicyclo-7-undecene) gives the same reaction products.
