Abstract:
Se provee un procedimiento para permitir una reacción de oxidación para producir eficientemente un ácido carboxílico aromático objetivo con una productividad eficiente al mejorar la actividad de un catalizador aún en la presencia de una cantidad relativamente pequeña de un catalizador; el procedimiento comprende oxidar con oxígeno un compuesto aromático que tiene un grupo alquilo y/o un grupo alquileno como un sustrato en la presencia de un catalizador que contiene una unidad imino cíclica que tiene un grupo N-OR (en donde R representa un átomo de hidrógeno o grupo protector para un grupo hidroxilo) y un co-catalizador de metal de transición (un compuesto de cobalto, un compuesto de manganeso, y un compuesto de circonio) para producir el ácido carboxílico aromático correspondiente al compuesto aromático; la reacción de oxidación se realiza con la alimentación de una mezcla del catalizador y al menos un elemento seleccionado del grupo que consiste del sustrato, un intermediario de la reacción (por ejemplo, una cetona y un aldehído), y un producto de la reacción (por ejemplo, agua y un ácido carboxílico aromático) sucesivamente o continuamente al sistema de reacción de oxidación; la reacción de oxidación puede realizarse usualmente en la ausencia de un disolvente de reacción; la reacción puede conducirse con la remoción del agua producida por la reacción del sistema de la reacción.
Abstract:
Preparation of lactam (I), comprises: converting cycloalkane with nitrous acid ester in presence of nitrogenous cyclic compound (a) to corresponding cycloalkanonoxime; subjecting the cycloalkanonoxime to Beckmann-rearrangement; and removing (a) and/or terminating the converting step. Preparation of lactam (I), comprises: converting cycloalkane with nitrous acid ester in presence of nitrogenous cyclic compound (a) to form corresponding cycloalkanonoxime, where (a) comprises dicarbonyl amine compound of formula (a1); subjecting the cycloalkanonoxime to Beckmann-rearrangement; and removing (a) and/or terminating the converting step. X : O or -OR; and R : H or OH. An independent claim is included for the preparation of the cycloalkanonoxime by the above process. [Image].
Abstract:
PROBLEM TO BE SOLVED: To provide a method for producing an epoxy compound, by which the epoxy compound corresponding to an unsaturated compound having at least one carbon-carbon double bond can be produced in a high yield. SOLUTION: Provided is a method for producing the epoxy compound, characterized by epoxidizing the unsaturated compound having at least one carbon-carbon double bond with hydrogen peroxide in the presence of a basic nitrogen-containing compound and a catalyst comprising a tungsten compound, a quaternary ammonium salt and a phosphoric acid-related compound to produce an epoxy compound corresponding to the unsaturated compound. The epoxidation reaction may be performed under a condition of pH 2 to 7. COPYRIGHT: (C)2009,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a method for efficiently producing an exo form or an endo form of a carboxylic acid corresponding to the exo form from a compound having a skeleton of a 7-oxa-2-norbornanecarboxylic acid ester which is a mixture of the exo form and the endo form with high selectivity. SOLUTION: The compound (a 7-oxa-2-norbornanecarboxylic acid ester, a 7-oxa-5-norbornene-2-carboxylic acid ester, etc.) is hydrolyzed in the presence of a basic catalyst in an amount of 0.1-1.5 mol equivalents based on 1 mol of the exo form at -20 to 50°C hydrolytic temperature. In the method, the carboxylic acid corresponding to the exo form or the endo form can be obtained with high selectivity of ≥80 mol% based on the whole carboxylic acid. COPYRIGHT: (C)2009,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a new substituted aminoaryladamantane derivative capable of being simply produced from an easily available compound and capable of being easily induced into an aminoaryladamantane derivative useful as a raw material, etc., for a highly functional material. SOLUTION: This substituted aminoaryladamantane derivative is expressed by formula (1) [R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are identical to or different from one another and are each hydrogen, an aromatic cyclic group expressed by formula (2) (Z is an aromatic ring, R 7 is a hydrolyzable protecting group, R 8 is hydrogen, a hydrocarbon group or a hydrolyzable protecting group, and p is an integer of not less than 1, provided that two or more R 7 's and R 8 's are identical to or different from one another, when p is two or more, and the aromatic ring may have a substituent other than a substituent specified in the above) or a substituent other than the group expressed by formula (2), provided that at least one of R 1 , R 2 , R 3 , R 4 , R 5 and R 6 is a group expressed by formula (2)] or the like. COPYRIGHT: (C)2006,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide an industrial method for producing an 8-15C lactam compound in high efficiency at a low cost by allowing the rearrangement reaction of a cyclic oxime compound to proceed without generating a large amount of by-products such as ammonium sulfate. SOLUTION: The method for producing a lactam compound expressed by formula (2) (m is an integer of 7-14) comprises the rearrangement reaction of a cyclic oxime compound of formula (1) (m is same as defined above) in a non-polar solvent B in the presence of an aromatic compound A having a leaving group bonded to a carbon atom constituting the aromatic ring and containing a heteroatom or a carbon atom bonded with an electron attractive group as an atom constituting the aromatic ring. COPYRIGHT: (C)2008,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a 3-oxa-2-thiatricyclo[4.2.1.0 4,8 ]nonane derivative. SOLUTION: The nonane derivative represented by formula [R a is H or an alkyl; R 1 , R 2 , R 3 , R 4 are each H, an alkyl; R 5 , R 6 , R 7 are H, an alkyl, a substituted oxycarbonyl, cyano; X is methylene which may be substituted, O or S; (n) is 1 or 2]. COPYRIGHT: (C)2007,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a method for almost completely reactivating an iridium compound whose catalytic activity is deteriorated or lost and to provide a method for using the reactivated iridium compound as a catalyst and a method for producing an organic compound using the reactivated iridium compound as the catalyst. SOLUTION: A method for regenerating the iridium compound includes a step of reactivating the iridium compound whose catalytic activity is deteriorated or lost, by changing the ionic valence of the iridium in the iridium compound. COPYRIGHT: (C)2009,JPO&INPIT