Basf Aktiengesellschaft

Werner Fliege

Bernd Meissner

Christian Dudeck

Axel Nissen

Peter Horn

Roman Fischer

Gerd Heilen

Wolfgang Koernig

Norbert Petri

Hans Diem

Karl-Heinz Ross

Gunter Lehmann

Arnold Wittwer

Walter Himmele

Wolfgang Sauer

Otto Woerz

Hans Diehm

Ekkehard Sapper

Hardo Siegel

Werner Aquila

Dieter Voges

Walter Rebafka

Michael Horner

Hans-Juergen Quadbeck-Seeger

Peter Tonne

Gerhard Epple

Fritz Brunnmueller

Guenter Boettger

Gernot Teege

Wolfgang Muehlthaler

Frank Weiss

Gerd Heiien

Wolfgang Keernig

A process for removing formaldehyde from aqueous solutions of but-2-yne-1,4-diol by treating the solutions with an alkaline agent at an elevated temperature in the presence of hydrogen peroxide.

Process for removing formaldehyde from aqueous solutions of

Saturated aliphatic, cycloaliphatic and araliphatic aldehydes are prepared by selective hydrogenation of the corresponding olefinically unsaturated aldehydes with hydrogen in the liquid phase over a palladium-containing catalyst, using a catalyst system in which the active constituents are from 2 to 90% by weight of palladium and from 10 to 98% by weight of an oxide or a salt of a rare earth metal or of a mixture of different oxides and/or salts of this type.

Preparation of saturated aliphatic, cycloaliphatic and araliphatic

Aldehydes or ketones of not less than 4 or 5 carbon atoms, respectively, are manufactured in a one stage process in the liquid phase by subjecting aldehydes and/or ketones of not less than 2 or 3 carbon atoms, respectively, to an aldol condensation and hydrogenating the resulting olefinically unsaturated aldehyde, the catalyst used for the aldol condensation and hydrogenation containing nickel or cobalt or their mixtures, zinc oxide and at least one of the elements iron, arsenic, antimony, bismuth, gallium, indium, thallium, germanium, tin, lead, cadmium and mercury or compounds of the said elements.

Manufacture of carbonyl compounds

Diketones are prepared by oxidizing glycols in the presence of a silver catalyst and/or copper catalyst of a specific particle size, under specific temperature conditions and with a specific composition of the catalyst. The end products are starting materials for the preparation of dyes, drugs, plastics, scents, wrinkle-resist finishes and assistants for increasing the tear strength and resilience of fibrous materials, hardeners for use in the photographic industry, textile assistants for preventing shrinkage after washing, and paper assistants.

Preparation of diketones

Aliphatic hydroxycarbonyl compounds etherified with aliphatic groups are prepared by oxidizing hydroxyalcohols in the presence of a metal catalyst which consists of one or more layers, each of a particular weight and each containing particles of a particular size, the catalyst bed also having a particular total thickness, and the catalyst components used being silver and copper, with or without added copper/tin/phosphorus or silver alone. The etherified hydroxyaldehydes and hydroxyketones obtainable by the process of the invention are valuable starting materials for the preparation of dyes, pesticides, plastics and scents.

Manufacture of aliphatic hydroxycarbonyl compounds etherified with

Alkyl pyruvates are prepared by oxidizing alkyl lactates in the presence of a silver catalyst of a defined particle size, at from 450.degree. to 700.degree. C. The products are starting materials for the preparation of drugs, synthetic resins and plastics.

Preparation of alkyl pyruvates

Aromatic and araliphatic aldehydes are prepared by oxidizing corresponding alcohols with oxygen in the presence of a silver catalyst of a defined particle size, and under defined temperature conditions. The products are starting materials for the preparation of dyes, pesticides, plastics and scents.

Preparation of aromatic and araliphatic aldehydes

Aldehydes or ketones of not less than 4 or 5 carbon atoms, respectively, are manufactured in a one stage process in the liquid phase by subjecting aldehydes and/or ketones of not less than 2 or 3 carbon atoms, respectively, to an aldol condensation and hydrogenating the resulting olefinically unsaturated aldehyde, the catalyst used for the aldol condensation and hydrogenation containing a mixture of nickel and cobalt, zinc oxide and at least one of the elements iron, arsenic, antimony, bismuth, gallium, indium, thallium, germanium, tin, lead, cadmium and mercury or compounds of the said elements.

Aldol condensation and hydrogenation process using a catalyst of nickel

3-Methyl-2-buten-1-al is prepared by isomerizing 3-methyl-3-buten-1-al in the presence of acidic or basic compounds. The product is a starting material for the manufacture of dyes, pesticides, pharmaceuticals, plastics and scents.

Preparation of 3-methyl-2-buten-1-al

4-(m,m'-ditert.-butyl-p-hydroxyphenyl)-butan-2-ones are produced by reaction of a 4-hydroxybutanone-(2) with 2,6-ditert.-butylphenol in the presence of a strong acid at elevated temperature. The compounds obtainable by the process, particularly 4-(m,m'-ditert.-butyl-p-hydroxyphenyl)-butane-2-one, are starting materials for the production of dyes, pest control agents and plastics auxiliaries and particularly of stabilizers for polyolefins and polyamides.

Production of 4-(m,m'-ditert.-butyl-p-hydroxyphenyl)-butan-2-ones

3-Alkyl-buten-1-als are prepared by oxidative dehydrogenation of 3-alkyl-buten-1-ols in the presence of a silver catalyst, of a particular total thickness, comprising 2 or more layers each of a particular weight and containing particles of a particular size. The products are starting materials for the manufacture of dyes, pesticides, drugs, plastics, naturally occurring materials and scents.

Preparation of 3-alkyl-buten-1-als

A process for the manufacture of higher ketones by reacting an aldehyde with a ketone in the presence of hydrogen over a catalyst system which contains, firstly, oxides or salts of the rare earth metals and, secondly, metals of group VIII of the periodic table of the elements. The process gives numerous higher ketones, required, for example, as solvents for surface coatings, or as scents, with high conversions and good selectivities, and therefore more simply and more economically than conventional methods.

Manufacture of higher ketones

Dyes of the formula ##STR1## where X is chlorine or bromine, Y is ##STR2## and n is 0, 1 or 2. On synthetic fiber materials, the dyes give clear blue colorations which are very fast to thermofixing and fast to light.

Anthraquinonoid disperse dyes

Novel 4-(m,m'-di-t-butyl-p-hydroxyphenyl)-butyl-2 compounds which are intermediates in the manufacture of dyes, pesticides and plastics auxiliaries, particularly stabilizers for polyolefins and polyamides. When molten, they form specific solvents for alkylphenols and are perfumes or form ingredients of perfume compositions having a fruity odor.

4-M,M'-Di-t-butyl-p-hydroxyphenyl) butyl-2 compounds

Novel 4-(m,m'-di-t-butyl-p-hydroxyphenyl)-butyl-2 diamides of aliphatic, araliphatic, cycloaliphatic or aromatic dicarboxylic acids which are intermediates in the manufacture of dyes, pesticides and plastics auxiliaries, particularly stabilizers for polyolefins and polyamides. When molten, they form specific solvents for alkylphenols and are perfumes or form ingredients of perfume compositions having a fruity odor.

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Otterstadt, Germany

Werner Fliege