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Bis-acenaphthyls

Significant shortcomings of such a technique for the preparation of 4,4 -keto-bis(naphthalic anhydride) are low yields of bis-acenaphthyls (4,4 -diacenaphthylmethane-15% 4,4 -diacenaphthyl ketone-5 %) and work with phosgene and carbon disulfide. [Pg.122]

This bisfnaphthalic anhydride) was prepared from acenaphthene derivative-4,4 -diacenaphthyl sulfone, which was synthesized by the interaction of acenaphthene with a mixture of dimethybulfate and sulfuric anhydride [94] or chlorosulfonic acid [95]. Sulfone-bis-(4,5-dicarboxynaphthyl l) dianhydride results from oxidation of bis-acenaphthyl with potassium permanganate in pyridine [94] ... [Pg.124]

Its isomer 2,2 -sulfone-bi naphthalic anhydride) resulted from sulfonation of acenaphthene with chlorosulfonic acid at 125-130 °C and subsequent oxidation of the obtained bis-(acenaphthyl)-sulfone with chromium anhydride [95] ... [Pg.124]

Another important group of bis(naphthalic anhydrides) - the so called bis(ketonaphthalic anhydrides) - was formed by the Fri lel-Crafts reaction between aromatic dicarboxylic acids dichlorides and two-fold molar amounts of acenaphthene and subsequent oxidation of tte obtained bis-acenaphthyls to bis(ketonaphthalic anhydrides) [111-115] according to heme 24. [Pg.129]

Oxidation of bis-acenaphthyls Interaction of bis-fo-phenyl-enediamine) with 4-(phenyl glyoxalyl) naphthalic anhydride... [Pg.136]


See other pages where Bis-acenaphthyls is mentioned: [Pg.120]    [Pg.225]    [Pg.120]    [Pg.120]    [Pg.225]    [Pg.120]    [Pg.383]    [Pg.383]    [Pg.135]    [Pg.135]   
See also in sourсe #XX -- [ Pg.119 , Pg.128 ]




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Acenaphthyle

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