Abstract: Saturated, fluorine-containing and chlorine-free hydrocarbons are prepared by catalytically hydrogenating unsaturated, fluorine- and chlorine-containing hydrocarbons at temperatures above 80.degree. C. in the gas phase.

Abstract: Acylbenzenes of the formula ##STR1## can be prepared by reaction of benzene with carboxylic acids of the formulaHOOC--R.sup.1 (II)where R.sup.1 has the meaning given in the text, using a molar ratio of benzene:carboxylic acid=1-50:1 at a temperature of 200.degree.-400.degree. C., a zeolite of the Pentasil type having an SiO.sub.2 /M.sup.2 O.sub.2 ratio of 15-500:1 being used as acid catalyst; in the latter formula, M.sup.2 is one element or more from the group comprising Al, B, Ga, In, Fe, Cr, V, As and Sb.

Abstract: A process for the preparation of a substituted 2-chloropyridine derivatives of the formula ##STR1## in which R.sup.1, R.sup.2, R.sup.3 and R.sup.4 represent hydrogen or various other radicals, which comprises reacting a pyridine-1-oxide of the formula ##STR2## with an aromatic carbonyl chloride in the presence of an inert organic solvent and in the presence of an acid acceptor at a temperature between about -20.degree. C. and 200.degree. C.

Abstract: A process for the preparation of aniline by hydrogenation of nitrobenzene in the gas phase in the presence of a catalyst containing a noble metal is described. The process can be carried out in an improved manner if the catalyst employed is palladium on graphite or petrol coke, as the support, containing 0.001-1% by weight of Pd, based on the total weight of the catalyst, it being possible for the catalyst also to contain, in addition to the Pd, 0.001-0.5% by weight of Ir and/or 0.001-0.3% by weight of Rh, all figures being based on the total weight of the catalyst.

Abstract: Di-(4-aminocyclohexyl)-methane containing 15 to 25% by weight of the trans-trans isomer can be obtained by the catalytic hydrogenation of di-(4-aminophenyl)-methane at elevated temperature and elevated hydrogen pressure in the presence of a ruthenium-containing supported catalyst containing 0.05 to 5% by weight ruthenium on an Al.sub.2 O.sub.3 support which has been treated with compounds of rare earth metals and manganese.

Abstract: Bismuth/alkaline earth metal catalysts which contain 0.005-0.8 g-atom of bismuth per mol of the alkaline earth metal compound employed and can furthermore contain promoters and/or inert additives, and lanthanide catalysts with or without catalyst supports can be employed as catalysts for halogen-fluorine exchange in organic compounds by means of hydrogen fluoride.

Abstract: Polychloro-fluoro-cyclopentenes can be prepared by catalytic reaction of hexachlorocyclopentadiene with hydrogen fluoride in the gas phase with the addition of chlorine.

Abstract: Aromatic amines, alkylated on the N-atom, can be prepared by catalytic alkylation of aromatic amines with alcohols or the corresponding ethers or by transalkylation with aromatic amines alkylated on the N-atom, whereby niobic acid or tantalic acid is used as the catalyst.

Abstract: 5-Fluoropyrimidines are obtained in an advantageous manner from halogenated 5-unsubstituted pyrimidines, when these are reacted with elemental fluorine in the presence of a solvent.

Abstract: Process for the preparation of polyaromatic compounds in which an aromatic dichloro compound, optionally in the presence of an anhydrous aprotic solvent, is reacted with metallic zinc, manganese or magnesium in the presence of a catalyst system of(1) from 0.1 to 25 mol-% (based on the dihalogen compound) of a nickel salt, nickel complex salt or nickel complex,(2) from 2 to 100 mol per mol of nickel in (1) of a triarylphosphine and optionally(3) from 0.1 to 10 mol per mol of nickel (1) of a halide, sulphate or phosphate of an alkali metal, alkaline earth metal, zinc, magnesium or manganese.

Abstract: The novel copper catalyst on an Al.sub.2 O.sub.3 -containing carrier which is impregnated with compounds of manganese and of one or more rare earth metals, having a Cu content of 0.1-5% by weight, a total content of compounds of manganese and of the rare earth metal or metals of 0.05 to 8% by weight, calculated as metals, is described, the weight ratio of rare earth metal(s) to manganese being 5:1-1:5, calculated as metal, and all percentages being relative to the total weight of the catalyst. Such catalyst is prepared by first impregnating the carrier with compounds of manganese and of the rare earth metal or metals, then fixing the copper salt on the impregnated carrier and activating the catalyst in a preferred manner by treatment with H.sub.2 at 150.degree. to 350.degree. C. Such a catalyst is suitable, for example, for the N-alkylation of aromatic amines with alkanols, where the aromatic amines can be prepared from the parent nitro compounds in an alkylation reactor with simultaneous addition of H.sub.2.

Abstract: Trifluoromethanesulphenyl chloride is prepared by reacting bis-(trifluoromethyl)disulfane in the liquid phase with chlorine in the presence of a strong acid.

Abstract: 4-Substituted 5-chloro-2-hydrazinothiazoles of the formula ##STR1## in which R represents CHF.sub.2, CF.sub.3, CN or COOR.sup.1, whereR.sup.1 represents C.sub.1 -C.sub.4 -alkyl.They are useful as pesticides and as intermediates for other pesticides.

Abstract: Process for the preparation of nuclear-fluorinated trifluoromethylbenzaldehydes from nuclear-chlorinated trifluoromethylbenzaldehydes, and new nuclear-fluorinated trifluoromethylbenzaldehydes.

Abstract: Unsymmetric biaryl compounds are prepared by coupling two different halogenoaromatics by reaction with a metal and carrying out the reaction in the presence of catalytic amounts of a nickel compound, a promoter and a phosphorus-containing ligand.

Abstract: The selective hydrogenation of unsaturated compounds which carry reducible groups containing nitrogen succeeds in a homogeneous phase with the preservation of the reducible groups containing nitrogen, characterized in that a compound of the formulaRuH.sub.2n L.sub.5-nis used as a catalyst, in whichL signifies a phosphane or arsane andn signifies 1 or 2.

Abstract: Aromatic, ring-fluorinated compounds are particularly advantageously prepared by nucleophilic exchange in the course of reaction wih potassium fluoride in the presence of phase transfer catalysts and, if desired, solvents by carrying out the reaction in the additional presence of metal salts.

Abstract: Benzotrifluorides substituted by fluorine and optionally in addition by chlorine, some of which are new, are prepared by hydrogenating benzotrifluorides which are substituted by fluorine and chlorine, in the presence of a catalyst and a hydrogen chloride acceptor.

Abstract: Benzotrifluorides substituted by fluorine and optionally in addition by chlorine, some of which are new, are prepared by hydrogenating benzotrifluorides which are substituted by fluorine and chlorine, in the presence of a catalyst and a hydrogen chloride acceptor.

Abstract: The selective hydrogenation of unsaturated compounds which carry reducible groups containing nitrogen succeeds in a homogeneous phase with the preservation of the reducible groups containing nitrogen, characterized in that a compound of the formulaRuH.sub.2n L.sub.5-nis used as a catalyst, in whichL signifies a phosphane or arsane andn signifies 1 or 2.