Abstract: The invention concerns a selective hydrodehalogenation method characterised in that it comprises a step which consists in contacting a substrate including a sp 3 hybridisation carbon atom bearing an electro-attracting group and at least a fluorine atom, and a halogen atom heavier than fluorine, with a reagent comprising: an aqueous phase, a base, a group VIII metal as hydrogenation catalyst, and hydrogen dissolved in the aqueous phase, at a concentration in equilibrium with a gas phase whereof the partial pressure in hydrogen is not less than 50 kPa, advantageously ranging between 50 kPa and 2.10 7 Pa. The invention is applicable to organic synthesis.

Abstract: The present invention relates to new metal compounds, to a process for the preparation of these metal compounds and to their use as catalysts.The new metal compounds according to the invention have, when they are used as catalysts, in particular as hydrogenation catalysts, an efficiency of the same order as that obtained with Raney nickel or cobalt.These metal compounds are more precisely compounds containing one or a number of divalent metals at least partially in the reduced state, bulked by a phase comprising one or a number of doping metals chosen from chromium, molybdenum, iron, manganese, titanium, vanadium, gallium, indium, bismuth, yttrium, cerium, lanthanum and the other trivalent lanthanides, in the form of oxides.

Abstract: The instant invention relates to a process for the preparation of fluoroanilines of formula (I) wherein a fluorinated nitrated benzene compound of formula (II) is subjected to a catalytic hydrogenation in a liquid medium containing a catalyst, under hydrogen pressure, carrying out a catalytic reduction reaction and, optionally, a hydrogenolysis reaction, wherein the compound of formula (II) is introduced gradually into the said medium so that the content of compound of formula (II) in the liquid remains less than or equal to 1000 ppm by mass, in order selectively to form the compound of formula (I).

Abstract: The invention relates to a method of doping a Raney nickel catalyst doped with metals by the incorporation of the doping metals in the form of a complex into the alkaline attack medium. Also disclosed is a process for the hydrogenation of nitriles to amines using said catalyst.

Abstract: The present invention relates to the field of the catalytic hydrogenation of nitrites to amines and, more particularly, of dinitriles such as adiponitrile (ADN) to diamines such as hexamethylenediamine (HMD).More precisely, the present invention relates to a process for the preparation of a catalyst for the hydrogenation of nitriles to amines of Raney nickel type doped with at least one additional metal element selected from columns IVb, Vb and VIb of the periodic classification.It is targeted at providing an economic and easy-to-implement process which makes it possible to obtain catalysts which are both active and selective with respect to nitrites and stable.The process is characterized in that it consists in suspending Raney nickel in a solution, preferably an acid solution, of the additional metal element.

Abstract: The present invention relates to the field of the catalytic reduction of nitriles to amines by use of Raney catalysts doped with one or a number of additional metal elements chosen from the elements of group IVb of the periodic classification.More precisely, it relates to a process for the hydrogenation of nitriles to amines, characterized in that it essentially consists:in selecting a liquid reaction medium which dissolves the nitrile substrate to be hydrogenated,in using at least one inorganic alkali metal or alkaline-earth metal hydroxide base,and in adopting a catalyst whose doping element/Ni ratio by weight is between 0.05 and 10%.More specific application to the hydrogenation of dinitriles to diamines or to aminonitriles.

Abstract: Halonitroaromatic compounds, e.g., 3-chloro-4-fluoronitrobenzene, are selectively hydrogenated into the corresponding haloaromatic amines, in the essential absence of hydrodehalogenation, by reacting same with hydrogen in the presence of a catalytically effective amount of a novel Raney-type catalyst composition consisting essentially of an alloy of nickel, aluminum and molybdenum, Ni/Al/Mo, the Al/Mo ratio by weight thereof being equal to or greater than 1.

Abstract: Halonitroaromatic compounds, e.g., 3-chloro-4-fluoronitrobenzene, are selectively hydrogenated into the corresponding haloaromatic amines, in the essential absence of hydrodehalogenation, by reacting same with hydrogen in the presence of a catalytically effective amount of a novel Raney-type catalyst composition consisting essentially of an alloy of nickel, aluminum and molybdenum, Ni/Al/Mo, the Al/Mo ratio by weight thereof being equal to or greater than 1.

Abstract: A process for the hydrogenation of halogenonitro-aromatic compounds wherein said compounds are contacted with a nickel-, cobalt- or iron-based catalyst, preferably Raney nickel, and hydrogen in the presence of a sulfur-containing compound. Preferably, the sulfur-containing compound is a sulfoxide or sulfone, and the molar ratio of the sulfur-containing compound to the catalyst ranges from about 1:1 to 10:1.

Abstract: A process for the preparation of amino halogeno aromatic compounds, according to which a halogenonitro-aromatic compound is brought into the presence of a nickel-, cobalt- or iron-based catalyst, preferably nickel-based, and, more preferably, Raney nickel, in the presence of an effective amount of iodide, at a temperature and hydrogen pressure sufficient to form said halogenoamino-aromatic compound.

Abstract: This invention relates to a process for preparation of a platinum-cobalt bi-metallic catalyst having an alloy structure.

Abstract: The present invention relates to a process for the industrial preparation of trifluoroethanol by passage of a reaction mixture containing trifluoroacetic acid, water and trifluoroethanol over a percolating fixed bed consisting of a rhodium- or ruthenium-based catalyst.

Abstract: 2-Methylpentanediamine is prepared by selectively liquid-phase hydrogenating a minimum concentration 2-methylglutaronitrile, initially nonammoniacal basic reaction medium in the presence of a catalytically effective amount of a Raney nickel-based catalyst, at a temperature of from 40.degree. to 150.degree. C., at a total pressure of less than 40 bars, and said reaction medium containing not more than 10% by weight of water.

Abstract: Unsaturated alcohols are prepared by hydrogenation of the corresponding carbonyl compounds in the presence of a platinum-cobalt bi-metallic catalyst having an alloy structure.

Abstract: A process is disclosed for the preparation of perfluoroalkanols by reacting an ester of a perfluorinated acid in the liquid phase with hydrogen under a pressure of between about 1 and 300 bars in the presence of a catalyst based on at least one metal selected from nickel, cobalt, copper and the metals of the platinum group. The perfluoroalkanols are employed as synthesis intermediates in the pharmaceutical and plant-protection industries.

Abstract: A process for preparing perfluoroalkanols by hydrogenation of the corresponding aliphatic perfluoroacids. An acid of the formula:C.sub.n F.sub.2n+1 COOHin which n is greater than or equal to 1, is reacted with hydrogen, in the presence of a catalyst based on ruthenium, rhodium, iridium or platinum, under a total pressure of between 1 and 50 bar and in the presence of at least one additive chosen from the group comprising the halide anions and the metal cations of columns IB, IIB, IVA, VA and VB of the periodic table of the elements.

Abstract: The invention relates to a process for the preparation of metachlorophenols.The process consists in selectively hydrodechlorinating, under the action of heat and in the liquid phase, polychlorophenols containing at least one chlorine atom in the meta position relative to the phenolic hydroxyl, by reacting these polychlorophenols with hydriodic acid in a quantity which is sufficient in relation to the chlorine atoms to be removed.The metachlorophenols obtained are organic synthesis intermediates.

Abstract: Process for the preparation of trifluoroethanol by the hydrogenation of trifluoroacetic acid in the liquid phase. The reaction is carried out in the presence of a catalyst based on ruthenium, rhodium, iridium or platinum, under a total pressure of between 5 and 50 bar, and with a ratio of the volume of the liquid phase used in the reactor to the total volume of the reactor of more than about 1/2. An absolute partial pressure of hydrogen of more than 1 bar is maintained during the reaction.

Abstract: Process for the selective preparation of metachloroanilines.It is carried out by the hydrodechlorination of polychloroanilines or polychloronitrobenzenes with hydrogen, in the liquid phase and in an acid medium, under the action of heat and under pressure, in the presence of a noble metal used in association with a heavy metal.These meta-chloroanilines are intermediates especially for active plant-protection substances.

Abstract: Process for the preparation of anilines substituted in the meta-position by a halogen atom.An aniline of the formula: ##STR1## in which: X' and X", R', R" and R"' are a halogen atom, alkyl (C.sub.1 -C.sub.4) or alkoxy (C.sub.1 -C.sub.4), one of the symbols X and one of the symbols R necessarily being a halogen and it being possible for one of the symbols X and one of the symbols R to be a hydrogen atom,is subjected to catalytic hydrogenation, in an anhydrous organic liquid phase, namely a chlorobenzene phase, in the presence of a halogen-containing hydracid and of a noble metal from group VIII of the periodic classification.