3.
    发明专利
    未知

    公开(公告)号:DE59106058D1

    公开(公告)日:1995-08-24

    申请号:DE59106058

    申请日:1991-09-25

    Applicant: HOECHST AG

    Abstract: PCT No. PCT/EP91/01829 Sec. 371 Date Mar. 23, 1993 Sec. 102(e) Date Mar. 23, 1993 PCT Filed Sep. 25, 1991 PCT Pub. No. WO92/05141 PCT Pub. Date Apr. 2, 1992.According to a process for producing isomer-free 2,3-difluoro-6-nitrophenol, 2,3,4-trifluoronitrobenzene is reacted with an aqueous solution of alkali metal or alkaline earth metal hydroxide in the absence of organic solvent, at temperatures between about 20 degrees C. and 100 degrees C., the pH value of the reaction mixture is set at about 1 to 6 by acid addition, the resulting product is stream distilled and the 2,3-difluoro-6-nitrophenol is isolated after cooling. No organic solvents are used during any of the steps of the process.

    PROCESS FOR THE PREPARATION OF 2,3-DIFLUORO-6-NITROPHENOL

    公开(公告)号:CA2092407A1

    公开(公告)日:1992-03-26

    申请号:CA2092407

    申请日:1991-09-25

    Applicant: HOECHST AG

    Abstract: PCT No. PCT/EP91/01829 Sec. 371 Date Mar. 23, 1993 Sec. 102(e) Date Mar. 23, 1993 PCT Filed Sep. 25, 1991 PCT Pub. No. WO92/05141 PCT Pub. Date Apr. 2, 1992.According to a process for producing isomer-free 2,3-difluoro-6-nitrophenol, 2,3,4-trifluoronitrobenzene is reacted with an aqueous solution of alkali metal or alkaline earth metal hydroxide in the absence of organic solvent, at temperatures between about 20 degrees C. and 100 degrees C., the pH value of the reaction mixture is set at about 1 to 6 by acid addition, the resulting product is stream distilled and the 2,3-difluoro-6-nitrophenol is isolated after cooling. No organic solvents are used during any of the steps of the process.

    PROCESS FOR THE PREPARATION OF 1,4-BIS(4-HYDROXYBENZOYL) BENZENE

    公开(公告)号:CA2072084A1

    公开(公告)日:1991-05-03

    申请号:CA2072084

    申请日:1990-10-25

    Applicant: HOECHST AG

    Abstract: Process for the preparation of 1,4-bis(4-hydroxyben-zoyl)benzene A process for the preparation of 1,4-bis(4-hydroxyben-zoyl)benzene of the formula (I) (I) by rearranging diphenyl terephthalate of the formula (II) (II) in about 3 to about 50 parts, relative to the diphenyl terephthalate, of an anhydrous organic solvent which is inert to the reactants, in the presence of about 30 to about 500 mol-% of a haloalkanesulfonic acid (catalyst) of the general formula (III) or (IV) Y(CnX2n)SO3H (III) Y(CnF2n)SO3H (IV), in which Y is a fluorine or hydrogen atom, and X is a fluorine and/or chlorine atom, with the proviso that at least one X is a fluorine atom, and n is an integer from 1 to 10, at temperatures of about 10 to about 200.degree.C.

    PROCESS FOR THE PREPARATION OF 2,3-DIFLUORO-6-NITROPHENOL

    公开(公告)号:CA2092407C

    公开(公告)日:1997-03-18

    申请号:CA2092407

    申请日:1991-09-25

    Applicant: HOECHST AG

    Abstract: According to a process for producing isomer-free 2,3-difluor-6-nitrophenol, 2,3,4-trifluornitrobenzol is reacted with an aqueous solution of alkali metal or alkaline earth metal hydroxide in the absence of organic solvent, at temperatures between about 20.degree.C and 100.degree.C, the pH value of the reaction mixture is set at about 1 to 6 by acid addition, the resulting product is steam distilled and the 2,3-difluor-6-nitrophenol is isolated after cooling. No organic solvents are used during any of the steps of the process.

    9.
    发明专利
    未知

    公开(公告)号:DE59007399D1

    公开(公告)日:1994-11-10

    申请号:DE59007399

    申请日:1990-06-25

    Applicant: HOECHST AG

    Abstract: PCT No. PCT/EP90/01002 Sec. 371 Date Feb. 24, 1992 Sec. 102(e) Date Feb. 24, 1992 PCT Filed Jun. 25, 1990 PCT Pub. No. WO90/00256 PCT Pub. Date Jan. 10, 1991.A process for the preparation of 1,4-bis(4-hydroxybenzoyl)benzene of the formula (I) (I) by reacting a 1,4-bis(4-halobenzoyl)benzene of the formula (II) (II) in which X is a fluorine, chlorine or bromine atom, with an alkali metal hydroxide or alkaline earth metal hydroxide or with mixtures of these hydroxides in a solvent which is inert to the reaction components under the reaction conditions at temperatures of about 100 DEG C. to about 250 DEG C., if appropriate in the presence of a phase transfer catalyst.

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