Abstract:
In a process for preparing methyl-nonyl-acetaldehyde from undecanal and formaldehyde or a source of formaldehyde, e.g., a substance which forms formaldehyde, in the presence of catalytic amounts of a secondary amine, the improvement whereinA. the undecanal is used in the form of the reaction mixture obtained by hydroformylation of 1-decene, andB. di-n-butylamine is used as the catalyst,C. the molar ratio of catalyst to undecanal is 0.025 to 0.050 to 1,D. the reaction is carried out at 90.degree. to 100.degree. C., andE. the 2-methylene-undecanal formed is then converted by partial hydrogenation into methyl-nonyl-acetaldehyde.
Abstract:
A process for selectively hydroformylating dicyclopentadiene to 8(9)-formyltricyclo-[5.2.1.02,6]dec-3-ene in a heterogeneous reaction system using an aqueous solution of transition metal compounds, containing water-soluble organic phosphorus(III) compounds in complex-bound form, of group VIII of the Periodic Table of the Elements, wherein the water-soluble organic phosphorus(III) compounds are alkali metal or alkaline earth metal salts of sulfonated arylphosphines and aryldiphosphines.
Abstract:
The present invention relates to a process for preparing aliphatic straight-chain and β-alkyl-branched carboxylic acids by catalytic oxidation of aldehydes by means of oxygen or oxygen-containing gas mixtures. Alkali metal carboxylates or alkaline earth metal carboxylates or a mixture thereof in an amount, calculated as alkali metal or alkaline earth metal, of from 1 mmol each to from 10 mmol each per mole of aldehyde used and also metals or compounds of metals of groups 5 to 11 of the Periodic Table of the Elements in amounts of not more than 5 ppm, based on aldehyde used, are present as catalyst.
Abstract:
The invention relates to a method for the synthesis of aliphatic carboxylic acids by the catalytic oxidation of aldehydes with oxygen, or oxygen-containing gas mixtures. Metals of groups 5 11 of the periodic table of elements, or the compounds thereof are used as catalyst, in amounts of up to 5 ppm, based upon the amount of aldehyde used.
Abstract:
A process for preparing saturated alcohols comprising effecting an aldol condensation of alkyl methyl ketones of 6 to 8 carbon atoms which are branched at the &bgr;-carbon atom with aldehydes of 4 to 15 carbon atoms which are branched at the &agr;-carbon atom to form &agr;,&bgr;-unsaturated ketones and subsequent hydrogenation of the &agr;,&bgr;-unsaturated ketones to obtain alcohols, wherein the aldol condensation is carried out at a temperature of 60 to 130° C. in the presence of a 30-55% strength aqueous solution of an alkali metal hydroxide resulting in very low by-product formation.
Abstract:
Isomeric mixtures of pentanoic acids are prepared by subjecting butene-1/butene-2 mixtures to hydroformylation to form aldehyde mixtures, followed by oxidation of the aldehyde mixtures which have been separated off from the reaction product. The hydroformylation is carried out in a heterogeneous system in the presence of rhodium catalysts which are dissolved in water. The mixture of isomeric 5 carbon monocarboxylic acids produced, when esterified with polyhydric alcohols, yields mixtures of isomeric esters which are useful as lubricants for refrigerant compressors operated with chlorine-free, at least partly fluorinated hydrocarbons as the refrigerant.
Abstract:
A process for the preparation of ethers of the formula R.sup.1 --CR.sup.2 .dbd.CH--O--R.sup.3, in which R.sup.1 and R.sup.3 are each a radical having 1 to 6 carbon atoms and R.sup.2 is hydrogen or a radical having 1 to 2 carbon atoms, by reaction of a diacetal of the formula R.sup.1 --CHR.sup.2 --CH(--O--R.sup.3).sub.2 in the presence of a catalyst composed of an acid and an amine at elevated temperature in the liquid phase. The unsaturated ether of the above-mentioned formula is formed from the diacetal with elimination of an alcohol R.sup.3 --OH.
Abstract:
Recovery of rhodium from the distillation residues from the crude products of oxo synthesis, the residue or the starting material containing the residue is treated with oxygen or an oxygen-containing gas in the presence of a monocarboxylic acid with 2 to 5 carbon atoms and of an alkali metal salt of a monocarboxylic acid with 2 to 5 carbon atoms. The rhodium is subsequently extracted with water as a water-soluble compound.
Abstract:
A process for the preparation of 2-(4-chlorophenyl)-3-methylbutyric acid from 4-chlorobenzaldehyde by conversion of the benzaldehyde to 3-(4-chlorophenyl)-2-methylpropenal, 3-(4-chlorophenyl)-2-methylpropanol, 1-(4-chlorophenyl)-2-methylpropene-1, and 2-(4-chlorophenyl)-2-methylbutyraldehyde, and finally to the desired corresponding butyric acid.
Abstract:
Preparation of 2,2-dimethylpropanediol-1,3 by the aldol addition of isobutyraldehyde and formaldehyde using tri-n-propylamine as a catalyst, followed by hydrogenation of the reaction mixture, and subsequent distillation of the hydrogenation product in the presence of isobutanol and water.