Abstract: Higher &agr;,&bgr;-unsaturated alcohols are prepared by monoethynylation of a ketone by the NH3/KOH method, if desired hydrogenation of the acetylene alcohol in the presence of hydrogen over a Pd-containing thin layer catalyst, purifying distillation of the hydrogenation product, preferably in a dividing wall column with recirculation of the unreacted ketone to the ethynylation step, and, if desired, preparation of higher alcohols having in each case 5 more carbon atoms in the chain by reacting the alcohols prepared by monoethynylation and, if desired, partial hydrogenation with alkyl acetoacetatesor diketene in a Carroll reaction to form ketones and using these as starting materials for the steps ethynylation, optional hydrogenation and fractional distillation.

Abstract: A process for the storage and transport of chloroformic acid esters in tanks or pipelines which have a plastic inside surface, which comprises using a plastic having a total nitrogen content of from 0 to 100 ppm by weight, where this plastic forms from 20 to 100% of the inside surface, and the use of tanks or pipelines of this type for the storage and transport of chloroformic acid esters.

Abstract: A process for preparing vinylphosphonic acid compounds of the formula (I) where R1 and R2 are, independently, H, C1-16-alkyl, C6-12-aryl, C7-12-alkaryl or C7-12-aralkyl, it being possible for the organic radicals to be substituted by one or more halogen atoms, hydroxyl, acyl or acetoxy groups, by reacting phosphorous acid compounds of the formula (II) with acetylene in the presence of a Pd(O) complexe or Pt(O) complex as catalyst.

Abstract: A process for hydrogenating an anthraquinone compound or a mixture of two or more thereof utilizes specific catalysts comprising, as active metal, a metal of transition group VIII of the Periodic Table of the Elements.

Abstract: A process for oxidizing an organic compound having at least one C—C double bond or a mixture of two or more thereof comprises the following steps:

Abstract: The invention relates to a process for the preparation of acid chlorides by reaction of carboxylic acids, carboxylic anhydrides, cyclic carboxylic esters or sulfonic acids with phosgene in the presence of a catalytic amount of a compound from the group consisting of N,N,N′,N′-tetrasubstituted amidinium halides (I), N,N,N′-trisubstituted amidinium hydrohalides (II) and N,N,N′-trisubstituted amidines (III).

Abstract: In a process for reacting an organic compound in the presence of a catalyst comprising, as active metal, at least one metal of transition group VIII of the Periodic Table, either alone or together with at least one metal of transition group I or VII of the Periodic Table, in an amount of from 0.01 to 30% by weight, based on the total weight of the catalyst, applied to a support containing macropores, the support comprises, as a support component, boron(III) oxide in an amount of from 10 to 100% by weight, based on the total weight of the support.

Abstract: In the process for the preparation of vinylsilanes by reacting acetylenic hydrocarbons with silanes which have at least one silicon-bonded hydrogen atom in the liquid phase in the presence of a catalyst, the silane is added to the liquid phase. In particular, the reaction is carried out at superatmospheric pressure, and the spent acetylenic hydrocarbon is replenished during the reaction while maintaining a pressure which is constant during the entire reaction.

Abstract: Alkenylphosphonic acid derivatives are prepared by reacting phosphonic acid derivatives with alkynes in the presence of a metal complex catalyst system comprising

Abstract: The invention relates to a process for preparing 1-substituted 5- and/or 3-hydroxypyrazoles of the formulae I and II in which R1 is C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl or C1-C4-alkoxy, where these groups may be substituted by halogen, C1-C4-alkoxy, phenoxy, C1-C6-alkoxycarbonyl, C1-C6-alkylthiocarbonyl or by a cyclic ring system having 3-14 ring atoms, which comprises reacting an alkyl 3-alkoxyacrylate of the formula III in which R2, R3 independently of one another are C1-C6-alkyl or C3-C6-cycloalkyl with a hydrazine of the formula IV in which R1 is as defined above a) at a pH of 6-11 to give 5-hydroxypyrazoles of the formula I or b) at a pH of 11-14 to give 3-hydroxypyrazoles of the formula II.

Abstract: A process for the reaction of an organic compound in the presence of a catalyst comprising, as active metal, ruthenium alone or together with at least one Group Ib, VIIb, or VIIIb metal in an amount of from 0.01 to 30 wt %, based on the total weight of the catalyst, applied to a support, wherein from 10 to 50% of the pore volume of the support comprises macropores having a pore diameter in the range of from 50 nm to 10,000 nm and from 50 to 90% of the pore volume of the support comprises mesopores having a pore diameter in the range of from 2 to 50 nm, the sum of said pore volumes being 100%, and said catalyst as such.

Abstract: The present application describes a process for preparing compounds of the indole type of the formula in which A is a hydrocarbon radical which, together with the carbons to which it is attached, forms a substituted or unsubstituted mono- or polycyclic aromatic system which may contain one or more heteroatoms from the group consisting of N, O and S, and R1, R2 independently of one another are H, a saturated, linear or branched aliphatic C1-C20-hydrocarbon radical, an unsaturated, linear or branched aliphatic C2-C20-hydrocarbon radical, a saturated or unsaturated, unsubstituted or alkyl-substituted cycloaliphatic C3-C20-hydrocarbon radical or an aromatic C5-C20-hydrocarbon radical, where these radicals may contain in their molecular skeleton one or more heteroatoms from the group consisting of the halogens, N, P, O, S, Si, Sn and B and may be substituted or unsubstituted, by cyclization of alkynylaminoaromatics of the formula in which R1 and R2 are as defined in formula (I)

Abstract: The process for preparing alkynediols of the formula (I) R1R2C(OH)—C≡C—C(OH)R1R2  (I) where R1, R2 are each independently H, or a C1-20-hydrocarbon radical which may be substituted by one or more C1-6-alkyls and/or be interrupted by nonadjacent heteroatoms and/or contain C—C double or triple bonds, by reacting compounds of the formula (II) R1—C(═O)—R2  (II) with acetylene in a polar aprotic solvent is carried out in the presence of basic alkali metal salts as catalysts.

Abstract: In a process for preparing carbonyldiimidazole of the general formulae Ia, Ib, Ic or mixtures thereof where R1 is hydrogen or a C1-4-alkyl radical and R2 is hydrogen or a methyl radical, by reacting at least one imidazole of the general formulae IIa and IIb in which R1 and R2 have the abovementioned meaning, with phosgene in an inert solvent, stoichiometric amounts, based on the imidazoles, of an organic nitrogen base which has a lower pKb than imidazole are added to the reaction mixture.

Abstract: The invention relates to a process for the preparation of &agr;-chloronitriles by reaction of cyanohydrins of aldehydes or ketones with phosgene using a phosphine oxide as catalyst.

Abstract: The present invention relates to a process for preparing a catalyst by activating a catalytic composition which comprises a) at least one metal of group IB or IIB or a compound thereof, b) where appropriate a carrier which comprises treating the composition with an alkyne of the general formula I R1—C≡C—R2  (I) in which R1 is alkyl, cycloalkyl, aryl, hydroxyalkyl, haloalkyl, alkoxy or alkoxyalkyl, R2 is a hydrogen atom, alkyl, cycloalkyl or aryl, and a carbonyl compound of the general formula II in which R3 and R4 are, independently of one another, a hydrogen atom, alkyl, haloalkyl, cycloalkyl or aryl, to catalysts obtainable by this process, and to alkynylations and aminoalkylations employing these catalysts.

Abstract: A process for hydrogenating benzenepolycarboxylic acids or a derivatives thereof by bringing one or more benzenepolycarboxylic acids or derivatives thereof into contact with a hydrogen-containing gas is carried out in the presence of a catalyst containing macropores. The catalyst contains, as an active metal, at least one metal of transition group VIII of the Periodic Table alone or together with at least one metal of transition group I or VII of the Periodic Table. Except that hydrogenation of dimethyl terephthalate using a catalyst containing ruthenium as active metal, either alone or together with at least one metal of transition group I, VII or VIII of the Periodic Table, applied to a support having a mean pore diameter of at least 50 nm and a BET surface are of at most 30 m2/g, where the active metal is present in an amount of from 0.01 to 30% by weight, based on the total weight of the catalyst, and the ratio of the surface areas of the active metal and the catalyst support is less than 0.

Abstract: Process for producing butyrolactones of the general formula I where R1 and R2 are each hydrogen, alkyl, hydroxyalkyl, substituted or unsubstituted aryl or substituted or unsubstituted trialkylsilyl, by reacting alkynes of the general formula II where R1 and R2 are each as defined above, with carbon monoxide and water in the presence of a rhodium catalyst under pressures from 20 to 300 bar and hydrogenating the unhydrogenated 2(5H)-furanone intermediates comprises a) reacting the carbonylation reaction mixture with hydrogen at from 150 to 250° C. and from 100 to 300 bar, b) removing the precipitated catalyst and returning it into the carbonylation reaction, and c) subjecting the catalyst-free reaction mixture to a distillation to recover the butyrolactone.

Abstract: In the process for the preparation of vinylsilanes by reacting acetylenic hydrocarbons with silanes which have at least one silicon-bonded hydrogen atom in the liquid phase in the presence of a catalyst, the silane is added to the liquid phase. In particular, the reaction is carried out at superatmospheric pressure, and the spent acetylenic hydrocarbon is replenished during the reaction while maintaining a pressure which is constant during the entire reaction.

Abstract: A process for hydrogenating an anthraquinone compound or a mixture of two or more thereof utilizes specific catalysts comprising, as active metal, a metal of transition group VIII of the Periodic Table of the Elements.