摘要:
Substituted 2-haloanilines are prepared from the correspondingly substituted 2,4-dichloro- or 2,4-dibromoanilines by selectively reducing a chloro or bromo substituent para to a protected amino group in the presence of the same halogen as an ortho substituent. The selective reductions are accomplished by protecting the amino function of the aniline with two protecting groups, e.g., as the diacetanilide or the succinimide.
摘要:
Novel substituted styrene compounds of the formula ##STR1## wherein R is halogen or --CF.sub.3 ; n is an integer from 0 to 5; and X.sub.1, X.sub.2, X.sub.3, X.sub.4 and X.sub.5 are halogen, and are useful as intermediates for preparing herbicidal compounds.
摘要翻译:新颖的取代苯乙烯化合物,其中R是卤素或-CF 3; n为0〜5的整数, X 1,X 2,X 3,X 4和X 5为卤素,可用作制备除草化合物的中间体。
摘要:
The invention is a process for coupling 2-naphthols which comprises contacting 2-naphthols dissolved in a polar acidic solvent in the presence of a catalytic amount of a catalyst which comprises a readily reducible form of a Group IB, Group VIII or manganese metal in the further presence of oxygen or a source of oxygen, under conditions such that 1,1'-bi-2-naphthol is prepared.
摘要:
Novel 1,4-Dithiinopyrazinetetracarbonitriles are disclosed. Their method of use in the control and kill of bacteria and fungi, and compositions containing the novel compounds as the active ingredients therein are claimed.
摘要:
The rate of photochlorination of methyl aromatic compounds, such as toluene, cresol, xylene, toluenesulfonyl chloride, methylnaphthalene, diphenylmethane, etc., is increased when carried out in the presence of bromine.
摘要:
Compounds are prepared corresponding to the formula ##STR1## WHEREIN R represents hydrogen or methylenethiocyanate (--CH.sub.2 SCN) and each of R.sup.1 and R.sup.2 represents loweralkyl of 1 to 4 carbon atoms. Those compounds wherein R is methylenethiocyanate have been found to be active antimicrobial agents and those wherein R is hydrogen are useful as intermediates therefor.
摘要:
The title compound is made by the direct bromination of citraconic anhydride in the vapor phase at 200.degree.-500.degree. C. with a contact time of less than about 20 seconds. The reactants are preferably diluted with an inert solvent, such as a halogenated hydrocarbon and/or a gaseous diluent, such as N.sub.2.