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Lignin hydrogenation, dimers from

The Structure of Dimers from the Alkaline Hydrogenation of Lignin... [Pg.262]

A third dimer was obtained from Norway sprucewood in somewhat impure condition (m.p., 117°-127°C.). However, its vapor phase retention time and ultraviolet spectrum 23) were identical with those of authentic 5,5 -diethyl-2,2 -dihydroxy-3,3 -dimethoxybiphenyl (VII), m.p. = 143°C. (P). Furthermore, the NMR spectrum and melting point of its purified diacetate were identical with those of the synthetic compound. The corresponding 5,5 -di-w-propyl derivative has already been isolated from neutral hydrogenation of softwood lignin in our laboratory 18). [Pg.267]

In summary, we have isolated and identified two dimeric compounds from the alkaline hydrogenation of sugar maplewood lignin—namely, 1,2-(4,4 -dihydroxy-3,3, 5,5 -tetramethoxydiphenyl)-ethane (I) l,2-(4,4 -... [Pg.267]


See other pages where Lignin hydrogenation, dimers from is mentioned: [Pg.262]    [Pg.264]    [Pg.147]    [Pg.367]    [Pg.409]    [Pg.68]    [Pg.497]    [Pg.518]    [Pg.253]    [Pg.271]    [Pg.129]    [Pg.184]    [Pg.72]    [Pg.504]    [Pg.294]    [Pg.457]    [Pg.61]   
See also in sourсe #XX -- [ Pg.249 ]




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