Abstract:
A process is disclosed for preparing anhydrous hydrazines by reacting a tertiary hydrazinium halide with a corresponding alkali metal or alkaline earth metal amide in the presence of a non-aqueous inert carrier.
Abstract:
The catalytic hydrogenation of o-nitro-chlorobenzene in aqueous alkali metal hydroxide solution with addition of an aromatic non-watermiscible solvent at an elevated temperature and under pressure using a noble metal catalyst and a polycyclic quinone as a co-catalyst leads to high and well-reproducible yields of 2,2'-dichloro-hydrazobenzene when the quinone is a derivative of anthraquinone, especially a hydroxy-anthraquinone. The product is obtained in so high a quality that it can be transformed without isolation or purification into 3,3'-dichlorobenzidine.
Abstract:
Novel polymers formed from the reaction of tetracarboxylic dianhydrides and hydrazines or hydrazides which may be cross-linkable by further reaction with a hydrazine or a hydrazide are disclosed.
Abstract:
Benzene-ring substituted (2-methylhydrazino)-methyl-benzene compounds and intermediates therefore are described. The former compounds are useful as cytostatic agents and, particularly, inhibit the growth of transplantable tumors in both mice and rats. Thus, they are active, for example, against Walker tumors, Ehrlich carcinoma and Ehrlich ascites carcinoma.
Abstract:
A process for preparing hydrazine hydrohalogenide is disclosed. The process comprises the steps of:(a) oxidizing benzophenone-imines with molecular oxygen in the presence of a copper halide catalyst to produce benzophenone-azines;(b) contacting the oxidation reaction mixture with an aqueous solution containing a hydrohalogenic acid thereby hydrolyzing the benzophenone-azines to produce a hydrazine hydrohalogenide and, simultaneously, extracting and removing the catalyst with the hydrohalogenic acid-containing aqueous solution to obtain an aqueous solution containing the hydrazine hydrohalogenide and the catalyst;(c) separating the aqueous solution and adjusting the solution to a pH of from 3 to 7 with an alkali;(d) contacting the aqueous solution with benzophenone-imines to extract the catalyst;(e) separating the catalyst-containing benzophenone-imines solution from the aqueous solution containing the hydrazine hydrohalogenide to recover the hydrazine hydrohalogenide and to recycle the catalyst-containing benzophenone-imines solution to step (a).The process is advantageous in that the catalyst is easily recovered for reuse.
Abstract:
A process for the production of 1-anthraquinonyl hydrazines of the formula ##STR1## wherein X is hydrogen or --NH--NH.sub.2, which comprises reacting 1-nitroanthraquinones of the formula ##STR2## wherein Z is hydrogen or nitro, in aprotic dipolar solvents, with hydrazine or hydrazine hydrate, at normal or slightly elevated temperature, to give 1-anthraquinonyl hydrazines of the formula (1).
Abstract:
Organic substituted hydrazines are prepared by introducing chloramine optionally carrying one or two alkyl groups into an intensely agitated or finely divided liquid, substantially anhydrous phase of a liquid primary or secondary amine or a solution of a primary or secondary amine in an inert solvent. Especially phenylhydrazine can be obtained in a very good yield from chloramine and aniline. The organic substituted hydrazines are important intermediates for syntheses, especially of pharmaceutical products.
Abstract:
3-amino-2,6-dinitrophenylhydrazines of the formula
WHEREIN Y is halogen, haloalkyl carbamyl, lower alkyl substituted carbamyl, carboxyl, lower alkoxy carbonyl, trifluoromethyl, nitro or cyano; Z is amino which is optionally substituted with lower alkyl, lower alkoxy, substituted lower alkyl, substituted lower alkoxy or mono or di-lower alkylamino, with the proviso that not more than one of the substituents is alkoxy, substituted alkoxy or mono or di-lower alkylamino; R1 is H, lower alkyl or lower alkenyl, said alkyl and alkenyl groups are optionally substituted with halogen, lower alkoxy, phenyl or cycloalkyl; R2 and R3 are independently H, C1-C5 alkyl, C2-C5 alkenyl, said alkyl and alkenyl groups are optionally substituted with cycloalkyl groups; R2 and R3 can also be taken together with the nitrogen atom to which they are linked forming the ring structures piperidino, hexamethylenimino, morpholino, or 4methylpiperazino. These compounds are very active plant growth regulators and are particularly useful as herbicides and in tobacco sucker control.
Abstract translation:3-氨基-2,6-二硝基苯肼,其结构式为:Y是卤素,卤代烷基氨基甲酰基,低级烷基取代的氨基甲酰基,羧基,低级烷氧基羰基,三氟甲基,硝基或氰基; Z是任选被低级烷基,低级烷氧基,取代的低级烷基,取代的低级烷氧基或单或二低级烷基氨基取代的氨基,条件是不超过一个取代基是烷氧基,取代的烷氧基或单或二 - 低级烷基氨基; R 1是H,低级烷基或低级烯基,所述烷基和烯基任选被卤素,低级烷氧基,苯基或环烷基取代; R2和R3独立地为H,C1-C5烷基,C2-C5烯基,所述烷基和烯基任选被环烷基取代; R2和R3也可以与它们所连接的氮原子一起形成环结构哌啶子基,六亚甲基亚氨基,吗啉代或4-甲基哌嗪基。
Abstract:
Fluoro-alkyl hydrazine compounds corresponding to the formula:
WHERE X is a hydrogen atom or a fluorine atom, R is hydrogen alkyl or aryl and n is a positive integer of from 1 to 25, and their method of preparation is described. The compounds are useful in preparing 1-fluoroalkyl-2-pyrazoline-5-one color couplers.