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Aminophenylmercuric acetate

SYNS (ACETATO)(p-AMNOPHENYL)MERCURY p-AMINOPHENYLMERCURIC ACETATE... [Pg.13]

AMINOPHENYL)(4-IMINO-2,5-CYCLOHEXADIEN-l-YLIDENE)METHYL), MONOCHLORIDE see RMK020 p-AMINOPHENYLMERCURIC ACETATE see ABQOOO... [Pg.1509]

When aniline is treated with mercuric acetate in aqueous solution at room temperature a mixture of o- and p-aminophenylmercuric acetates is formed,... [Pg.112]

The isomeric o-aminophenylmercuric acetate is difficult to separate from the larger amount of the p- compound which would separate with it if the filtrate from the initial crop of the p- acetate were allowed to stand. Dimroth found, however, that there was a considerable difference in the solubilities of the chlorides, so the filtrate is treated with an excess of sodium chloride solution, precipitating p-aminophenylmercuric chloride in the amorphous state, while the 0-amino chloride separates in crystalline form. The mixture is sucked off, dried, and the 0- derivative extracted with not too much warm alcohol, separating as leaflets after the solution is chilled and allowed to stand The amorphous residue of p- chloride may be boiled with alcohol or benzene, and separates from the cold solution as leaflets melting at 1880, with decomposition. [Pg.97]

The following p-aminophenylmercuric salts are obtained by the action of the corresponding alkali salts on. the acetate bromide, colourless lamina , M.pt, 182° C. iodide, M.pt. 165° C. (with decom-])Ositi(>n) nitrate, microscopic crystals sul Aiate, needles, M.pt. 150° C. (witli decomposition) thiosulphate, colourless plates, M.pt. 95° C. (with decomposition). [Pg.116]


See other pages where Aminophenylmercuric acetate is mentioned: [Pg.392]    [Pg.363]    [Pg.363]    [Pg.10]    [Pg.96]    [Pg.112]    [Pg.116]    [Pg.392]    [Pg.506]    [Pg.96]    [Pg.97]    [Pg.627]    [Pg.392]    [Pg.363]    [Pg.363]    [Pg.10]    [Pg.96]    [Pg.112]    [Pg.116]    [Pg.392]    [Pg.506]    [Pg.96]    [Pg.97]    [Pg.627]    [Pg.98]    [Pg.116]    [Pg.222]    [Pg.98]   


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