PROCESS FOR THE PREPARATION OF UREIDOPEROXYCARBOXYLIC ACIDS

    公开(公告)号:CA2055701A1

    公开(公告)日:1992-05-17

    申请号:CA2055701

    申请日:1991-11-15

    Applicant: HOECHST AG

    Abstract: HOE 90/F 347 : Process for the preparation of ureidoperoxycarboxylic acids. A process for the preparation of ureidoperoxycarboxylic acids of the formula , in which x is the number 1 or 2, A, if x is 1, is hydrogen, C1-C20-alkyl, aryl, preferably phenyl, or haloaryl, preferably chlorophenyl, or if x is 2, is C1-C20-alkylene or arylene, preferably phenylene, B is a group of the formula , , , or , in which n is a number from 1 to 20, m is the number 0, 1 or 2, R1 is C1-C20-alkyl and R2 is in each case hydrogen or C1-C20-alkyl, which comprises dissolving carbamoyllactams of the formula , in which x, A and B have the abovementioned meanings, in a one- to six-fold, preferably a one- to three-fold, amount by weight of a strong catalyst acid, by then adding water in a one- to ten-fold molar excess, relative to the carbamoyllactam, to the solution of the carbamoyllactam in the catalyst acid and by heating the reaction mixture to form the ureidocarboxylic acid, by then adding to the reaction mixture an aqueous hydrogen peroxide solution in a one- to ten-fold, preferably a two- to four fold, molar excess per oxidizable carboxyl group of the ureidocarboxylic acid formed in the preceding reaction step, and by then precipitating the resulting ureidoperoxycarboxylic acid from the reaction mixture. These compounds are suitable as bleaches, oxidants and disinfectants.

    PROCESS FOR THE PREPARATION OF UREIDOPEROXYCARBOXYLIC ACIDS

    公开(公告)号:ZA919057B

    公开(公告)日:1992-09-30

    申请号:ZA919057

    申请日:1991-11-15

    Applicant: HOECHST AG

    Abstract: A process for the preparation of ureidoperoxycarboxylic acids of the formula A[NHCONHBCOOOH]x, in which x is the number 1 or 2, A, if x is 1, is hydrogen, C1-C20-alkyl, aryl, preferably phenyl, or haloaryl, preferably chlorophenyl, or if x is 2, is C1-C20-alkylene or arylene, preferably phenylene, B is a group of the formula in which n is a number from 1 to 20, m is the number 0, 1 or 2, R1 is C1-C20-alkyl and R2 is in each case hydrogen or C1-C20-alkyl, which comprises dissolving carbamoyllactams of the formula in which x, A and B have the abovementioned meanings, in a one- to six-fold, preferably a one- to three-fold, amount by weight of a strong catalyst acid, by then adding water in a one- to ten-fold molar excess, relative to the carbamoyllactam, to the solution of the carbamoyllactam in the catalyst acid and by heating the reaction mixture to form the ureidocarboxylic acid, by then adding to the reaction mixture an aqueous hydrogen peroxide solution in a one- to ten-fold, preferably a two- to four fold, molar excess per oxidizable carboxyl group of the ureidocarboxylic acid formed in the preceding reaction step, and by then precipitating the resulting ureidoperoxycarboxylic acid from the reaction mixture. These compounds are suitable as bleaches, oxidants and disinfectants.

    PROCESS FOR THE PREPARATION OF UREIDOPEROXYCARBOXYLIC ACIDS

    公开(公告)号:AU8785691A

    公开(公告)日:1992-05-21

    申请号:AU8785691

    申请日:1991-11-15

    Applicant: HOECHST AG

    Abstract: A process for the preparation of ureidoperoxycarboxylic acids of the formula A[NHCONHBCOOOH]x, in which x is the number 1 or 2, A, if x is 1, is hydrogen, C1-C20-alkyl, aryl, preferably phenyl, or haloaryl, preferably chlorophenyl, or if x is 2, is C1-C20-alkylene or arylene, preferably phenylene, B is a group of the formula in which n is a number from 1 to 20, m is the number 0, 1 or 2, R1 is C1-C20-alkyl and R2 is in each case hydrogen or C1-C20-alkyl, which comprises dissolving carbamoyllactams of the formula in which x, A and B have the abovementioned meanings, in a one- to six-fold, preferably a one- to three-fold, amount by weight of a strong catalyst acid, by then adding water in a one- to ten-fold molar excess, relative to the carbamoyllactam, to the solution of the carbamoyllactam in the catalyst acid and by heating the reaction mixture to form the ureidocarboxylic acid, by then adding to the reaction mixture an aqueous hydrogen peroxide solution in a one- to ten-fold, preferably a two- to four fold, molar excess per oxidizable carboxyl group of the ureidocarboxylic acid formed in the preceding reaction step, and by then precipitating the resulting ureidoperoxycarboxylic acid from the reaction mixture. These compounds are suitable as bleaches, oxidants and disinfectants.

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