Abstract:
PROBLEM TO BE SOLVED: To provide a method for producing a 5-alkoxy-substituted oxazole, especially a 4-methyl-5-alkoxy-substituted oxazole and further a method for producing a pyridoxine derivative. SOLUTION: The method for producing the substituted oxazole is carried out as follows. An α-isocyanoalkanoic acid ester is converted into the 5-alkoxy- substituted oxazole in the presence of an assistant composed of an alcohol or an ester at >80°C. The resultant 5-alkoxy-substituted oxazole is taken out of the reactional mixture simultaneously with the conversion. COPYRIGHT: (C)2003,JPO
Abstract:
PROBLEM TO BE SOLVED: To economically prepare 2-alkyne-1-acetal with a high selectivity and in a high product yield. SOLUTION: In a preparation method of 2-alkyne-1-acetal of formula I (wherein substituents are as indicated in the patent claim), a compound of formula III (wherein R 1 is as indicated in formula I) is electrochemically oxidized either in the presence of a 1-6C alkyl alcohol (alcohol A) or in the form of a substance. COPYRIGHT: (C)2006,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide a method for producing a 5-alkoxy-substituted oxazole and a method for producing a pyridoxine derivative. SOLUTION: The 5-alkoxy-substituted oxazole is obtained by converting an α-isocyano alkylic acid ester in the presence of a base at >80°C and separating the 5-alkoxy-substituted oxazole from the reaction mixture simultaneously with the converting reaction, and the pyridoxine derivative is obtained by converting an amino acid into an amino acid ester, converting the obtained into a formamido acid ester, converting the obtained into an α-isocyanoalkyl acid ester, converting the obtained into a 5-alkoxy-substituted oxazole in the presence of a base at >80°C and separating the 5-alkoxy-substituted oxazole from the reaction mixture simultaneously with the converting reaction, reacting the obtained 5-alkoxy-substituted oxazole with a protective diol to obtain an Diels-Alder adduct and treating the obtained with an acid and removing the protective group to convert into the pyridoxine derivative. COPYRIGHT: (C)2003,JPO
Abstract:
The invention relates to a method for the production of orthoesters, wherein a first orthoester and a first alcohol are guided into a rectification column such that in at least one area of the column the first orthoester and the first alcohol react with a second orthoester and a second alcohol, and the second orthoester and the second alcohol are removed from the reaction area.
Abstract:
Disclosed is a method for separating acids from chemical reaction mixtures by means of an auxiliary base. Said auxiliary base b) forms a salt with the acid, which is liquid at temperatures at which the valuable product is not significantly decomposed during separation, and c) the salt of the auxiliary base and the valuable product or the solution of the valuable product form two immiscible fluid phases in a suitable solvent.
Abstract:
The present application describes a process for regenerating a ruthenium catalyst for the hydrogenation of benzene, which comprises flushing the catalyst with inert gas in a regeneration step until the original or part of the original activity is attained.
Abstract:
The present invention relates to a process for regenerating a ruthenium catalyst which is suitable for hydrogenation, which comprises flushing the catalyst with inert gas in a regeneration step until the original activity or part of the original activity is attained. The process is particularly suitable for ruthenium catalysts which are used for the hydrogenation of aromatics.
Abstract:
The present invention relates to a process for regenerating a ruthenium catalyst for the hydrogenation of phthalates, which comprises flushing the catalyst with inert gas in a regeneration step until the original activity or part of the original activity is attained.
Abstract:
A heterogeneous ruthenium catalyst comprises an amorphous silicium dioxide in the form of a support material and is produced by one or several impregnations of the support material with a rhenium salt solution, drying and reduction. Said invention is characterised in that the silicium dioxide support material has a BET surface (according to DIN 66131) ranging from 250 ti 440 m 2 /g, a pore volume (according to DIN 66134) ranging from 0.7 to 1.1 ml/g and a pore diameter (according to DIN 66131) ranging from 6 to 12 nm. The invention also relates to a method for producing a carboxylic aromatic group, in particular a method for producing bisglycidyl ethers of formula (I), wherein R is CH 3 or H, by hydrogenating the core of an aromatic bisglycidyl ether of formula (II) in which the heterogeneous ruthenium catalyst is introduced.
Abstract:
The invention relates to a shell catalyst containing ruthenium as an active metal, alone or together with at least one other metal of the auxiliary group IB, VIIB or VIII of the periodical system of the elements (CAS version), and applied to a carrier containing silicon dioxide as a carrier material. The invention also relates to a method for producing said shell catalyst, and to a method for hydrogenating an organic compound containing hydrogenable groups, preferably for hydrogenating a carbocyclic aromatic group to form the corresponding carbocyclic aliphatic groups or for hydrogenating aldehydes to form the corresponding alcohols, using the inventive shell catalyst. The invention further relates to the use of the inventive shell catalyst for hydrogenating an organic compound containing hydrogenable groups, preferably for hydrogenating a carbocyclic aromatic group to form the corresponding carbocyclic aliphatic groups or for hydrogenating aldehydes to form the corresponding alcohols.