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Methanetricarboxylic acid

Methanetricarboxylic Acid.—Mulliken1 employed the method, which has already been discussed (p. 104), in the electrolysis of the sodium salt of the triethyl ester of this acid and obtained othanehexacarboxylic ester, besides some malonic ester. Further oxidation caused the formation of sodium bicarbonate ... [Pg.117]

Diethyl cyanomalonate Dieth ester nitrile of methanetricarboxylic acid, cyanonudonic ester)... [Pg.798]

The oxidation of thioanilides of diethyl methanetricarboxylate (15 X = S) by bromine in polar solvents, especially formic acid, yields the corresponding benzothiazoles (17). An examination of the reaction under a variety of conditions suggests that sulphenyl bromides (16) function as intermediates. In non-polar solvents, desulphurization to the amides (15 X = O) becomes the predominating reaction. ... [Pg.620]

See other pages where Methanetricarboxylic acid is mentioned: [Pg.172]    [Pg.172]    [Pg.78]    [Pg.51]    [Pg.37]    [Pg.176]    [Pg.724]   
See also in sourсe #XX -- [ Pg.117 ]



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