Basf Se Corporation

Andreas Weickgenannt

Alexander Panchenko

Ralph Busch

Rolf Pinkos

Holger Friedrich

Jan-Oliver Weidert

Kai Thiele

Andreas Woelfert

Sandra Kramp

Artur Kozicki

Kirsten Dahmen

Nicole Holub

Regina Benfer

Martin Bock

Gerrit Waters

Klaus Breuer

Daniel Pfeiffer

Albert Werner

Bernd Bastian Schaack

Pawel Czajka

Lukas Schulz

Barbara Wucher

Michael Lorenz

Marta Porta Garcia

Norbert Gutfrucht

Oliver Christian Gobin

Alexander Duefert

Michael Hübner

Frank Hettche

Annebart Wentink

Simon Kokolakis

Viktor Ladnak

Wolfgang Gmeiner

Silvia Tauro

Aik Meam Tan

Marcus Reble

Andreas WÖLFERT

Described is a process for producing 1-(4-isobutylphenyl)ethanol by reacting 1-(4-isobutyl-phenyl)ethanone with hydrogen in the presence of a catalyst composition comprising cop-per and one or more metals other than copper, and a use of a respective composition and/or of a pre-composition, the pre-composition comprising a mixture of oxides of copper and oxides of one or more metals other than copper, in a catalytic hydrogenation process for producing 1-(4-isobutylphenyl)ethanol from 1-(4-isobutylphenyl)ethanone.

Process for producing 1-(4-isobutylphenyl)ethanol by hydrogenation of 1-(4-isobutyl-phenyl)ethanone in the presence of a catalyst composition comprising copper

The present invention relates to a process for hydrogenating a mixture (G1) in the presence of a catalyst, where the mixture (G1) comprises at least one colorless amine and at least one color-imparting component. As a result of the hydrogenation step, the at least one color-imparting component is firstly partially, preferably fully, hydrogenated, while the colorless amine, in particular aniline, is not hydrogenated or hydrogenated to only a very small extent. The color-imparting components which cause the discoloration of the amine which is itself in principle colorless are thus removed by hydrogenation, as a result of which purification of the colorless amine or the mixture (G1) is achieved.

Process for hydrogenating a mixture in the presence of a colorless amine

A process for preparing trans-enriched MDACH, including: distilling an MDACH starting mixture in the presence of an auxiliary, which is an organic compound having a molar mass of 62 to 500 g/mol, a boiling point at least 5&#xb0; C. above the boiling point of cis,cis-2,6-diamino-1-methylcyclohexane, and 2 to 4 functional groups, each of which is independently an alcohol group or a primary, secondary or tertiary amino group. The MDACH starting mixture includes 0 to 100% by weight of 2,4-MDACH and 0 to 100% by weight of 2,6-MDACH, based on the total amount of MDACH present in the MDACH starting mixture. The MDACH starting mixture includes both trans and cis isomers. Trans-enriched MDACH includes 0 to 100% by weight of 2,4-MDACH and 0 to 100% by weight of 2,6-MDACH, where the proportion of trans isomers in the mixture is higher than the proportion of trans isomers in the MDACH starting mixture.

Method for producing cis- and trans-enriched MDACH

A method for isomerizing a starting mixture comprising 2,4-diamino-1-methylcyclohexane, 2,4-MDACH for short, 2,6-diamino-1-methylcyclohexane, 2,6-MDACH for short, or mixtures thereof, wherein the isomerization is carried out in the presence of a supported catalyst with zirconium dioxide as support and ruthenium as active metal.

Isomerization of MDACH

The present invention relates to a process for hydrogenating 4,4'-methylenedianiline and/or polymeric MDA with hydrogen in the presence of a catalyst comprising ruthenium on a zirconium oxide support material, and also to the use of a catalyst comprising ruthenium on a zirconium oxide support material for hydrogenating 4,4&#x2032;-methylenedianiline and/or polymeric MDA.

Process for hydrogenating 4,4'-methylenedianiline

The present invention relates to a process for preparing cyclohexane from methylcyclopentane (MCP) and benzene. In the context of the present invention, MCP and benzene are constituents of a hydrocarbon mixture (HM1) additionally comprising dimethylpentanes (DMP), possibly cyclohexane and possibly at least one compound (low boiler) selected from acyclic C-C-alkanes and cyclopentane. First of all, benzene is converted in a hydrogenation step to cyclohexane (that present in the hydrocarbon mixture (HM2)), while MCP is isomerized in the presence of a catalyst, preferably of an acidic ionic liquid, to cyclohexane. After the hydrogenation but prior to the isomerization the dimethylpentanes (DMP) are removed, with initial removal of the cyclohexane present in the hydrocarbon mixture (HM2) together with DMP. This cyclohexane already present prior to the isomerization can be separated again from DMP in a downstream rectification step and isolated and/or recycled into the process for cyclohexane preparation. Between the DMP removal and MCP isomerization&#x2014;if low boilers are present in the hydrocarbon mixture (HM1)&#x2014;low boilers are, optionally removed. After the isomerization, the cyclohexane is isolated, optionally with return of unisomerized MCP and optionally of low boilers. Preferably, cyclohexane and/or low boilers are present in the hydrocarbon mixture (HM1), and so a low boiler removal is preferably conducted between the DMP removal from isomerization. It is additionally preferable that the removal of the cyclohexane from DMP is additionally conducted, meaning that the cyclohexane component which arises in the benzene hydrogenation and may be present in the starting mixture (HM1) is isolated and hence recovered.

Process for preparing cyclohexane from benzene and methylcyclopentane with upstream benzene hydrogenation

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Mannheim, Germany

Andreas Weickgenannt