Developing agents hydrazine

Functional biaryl derivatives are important industrial chemicals. They are used as monomers for the production of high performance and other polymers, as well as dyes, pharmaceuticals and agrochemical intermediates. We have developed an improved method for the dehalogeno-dimerization of aryl bromides to yield biaryl derivatives under mild conditions (temperature < 100°C, atmospheric pressure) using a common base, a 5 % Pd/C catalyst (0.1 - 10 % w/w, based on the starting material) in an aqueous medium and formyl hydrazine as the reducing agent. Several examples of biaryl derivatives are discussed. 

The procedure given here has been developed from the reaction with hypophosphite. Other reducing agents such as ethanol, hydrazine, or even molecular hydrogen6 are very effective catalysts and may be used instead of hypophosphite. 

This ammonium phosphomolybdate complex is yellow, but if mildly reduced by ascorbic acid in the presence of potassium antimonyl tartrate a solution of stable bluish-purple color ( molybdenum blue ) develops after about ten minutes, which has its strongest absorption at 882 pm (Fig. 4.6). Other mild reducing agents have also been used, including tin(II) chloride, or hydrazine sulfate, which give maximum absorbances at slightly different wavelengths. The intensity of the color which develops is linearly proportional to the... 

Uses Manufacture of acrylonitrile, hydrazine hydrate, hydrogen cyanide, nitric acid, sodium carbonate, urethane, explosives, synthetic fibers, fertilizers refrigerant condensation catalyst dyeing neutralizing agent synthetic fibers latex preservative fuel cells, rocket fuel nitrocellulose nitroparaffins ethylenediamine, melamine sulfite cooking liquors developing diazo films yeast nutrient. 

The essential difference between the hydroxylamine reaction and the hydrazine reaction appears to be that silver nuclei are formed in the solution much more readily by hydrazine than by hydroxylamine. At sufficiently low pH and in the absence of copper, hydroxylamine does not readily form nuclei in the solution, and the catalytic reduction of the silver chloride occurs essentially at a solid interface with the silver nuclei. Hydrazine, on the other hand, readily forms nuclei in the solution and an important fraction of the total reaction involves the catalytic reduction of dissolved silver chloride. This would account for the well-known photographic properties of the two agents. Hydroxylamine is a cleanworking developer which, under proper conditions, yields little fog. Hydrazine shows much less selectivity and, although it develops an image, it also yields a relatively high fog density. 

Although many antibiotics are effective to some extent in arresting the progress of tuberculosis, none is uniformly successful. One of the most effective is isonicotinic hydrazide (73), available from methyl isonicotinate by reaction with hydrazine (B-75MI20903). Extensive clinical use of this agent showed the drug to possess an additional antidepressant effect and led to the development of iproniazid (74), an established antidepressant (53JOC994). 

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