Dsm Fine Chemicals Austria Nfg Gmbh & Co. Kg

Curt Zimmermann

Gerhard Steinbauer

Peter Hildebrand

Engelbert Kloimstein

Michael Stanek

Alexander Sajtos

Erich Steinwender

Ernst Wressnegger

Marianne Castelijns

Helmut Sengstschmid

Willibald Scheuchenstuhl

The invention relates to a method for producing monocarbonyl compounds or biscarbonyl compounds or hydroxyl compounds by ozonizing, unsaturated organic carbon compounds that, per molecule, have one or more olefinic or aromatic double bonds, which can be cleaved by ozone, and by subsequently processing the ozonization products. According to the inventive method, unsaturated organic carbon compounds that, per molecule, have one or more olefinic or aromatic double bonds, which can be cleaved by ozone, are: (a) in 1 to 2 steps, continuously reacted with ozone in stoichiometric quantities or in excess while using counter educt currents and being in an organic solvent or in an aqueous solution inside a device, which consists of one to two absorption apparatuses, of devices for carrying away reaction heat, and of devices for separating the gas and liquid phases, and; (b) the peroxides resulting therefrom are, according to reaction parameters from step (a), converted into the corresponding monocarbonyl compounds or biscarbonyl compounds or hydroxyl compounds either by continuous or discontinuous hydrogenation, oxidation or heating.

Method for producing monocarbonyl compounds or biscarbonyl compounds or hydroxyl compounds

The invention relates to a method for the production of 2-coumarone or substituted 2-coumarones, whereby cyclohexanone or substituted cyclohexanone is reacted with a carboxyl-containing acylating agent a) to give methyl 2-(2-oxo-cyclohexyl)-2-hydroxyacetate or substituted methyl 2-(2-oxo-cyclohexyl)-2-hydroxyacetates, which are either a) directly converted to 2-coumarone or substituted 2-coumarones by means of catalytic gas-phase dehydrogenation, or a) dehydrated by means of azeotropic distillation under basic conditions, or by use of a strong acid, or a strongly acidic ion exchanger to a mixture of methyl 2-oxocyclohexylidenacetate and the enol-lactone of the 2-oxocyclohexylidenacetic acid, or a mixture of substituted methyl 2-oxocyclohexylidenacetate and the enol-lactone of the substituted 2-oxocyclohexylidenacetic acid, which is finally converted in turn by catalytic gas-phase dehydrogenation to 2-coumarone, or substituted 2-coumarones, or b) are directly converted under acidic or basic conditions into a mixture of methyl 2-oxocyclohexylidenacetate and the enol-lactone of 2-oxo-cyclohexylidenacetic acid, or a mixture of substituted methyl 2-oxocyclohexylidenacetate and the enol-lactone of the substituted 2-oxo-cyclohexylidenacetic acid, which is finally converted in turn by catalytic gas-phase dehydrogenation into 2-coumarone or substituted 2-coumarones.

Method for the production of 2-coumarone and substituted 2-coumarones

A process for reducing the amount of nitrification-inhibiting sulfur compounds in reaction solutions obtained by the sulfur-compound-catalyzed conversion of &agr;,&bgr;-unsaturated carboxylic acids into the corresponding trans or cis isomer, in which an oxidizing agent is added in molar deficiency up to a maximum of twice the molar amount, based on the catalyst compound, to the reaction mixture obtained after the termination of the isomerization and then isolating the corresponding trans or cis isomer in a known manner and working it up and supplying the resultant process waste waters to a biological cleanup stage.

Process for reducing the amount of nitrification-inhibiting sulfur compounds

An improved process for the preparation of substituted pyridinecarboxylic acids (II), useful as herbicide intermediates, by ozonolysis of quinolines (I).

Method for producing substituted pyridine-carboxylic acids

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Riedmark, Austria

Curt Zimmermann