33.
    发明专利
    未知

    公开(公告)号:DE3767119D1

    公开(公告)日:1991-02-07

    申请号:DE3767119

    申请日:1987-10-17

    Applicant: HOECHST AG

    Abstract: Styrylaryloxy ether sulfonates of the formula in which either R1 denotes styryl and simultaneously R2 and R3 are identical or different and denote hydrogen or styryl, or R1 and R2 are nonidentical and each denote methyl or styryl and simultaneously R3 denotes hydrogen or styryl, x denotes a number from 2 to 20, and M denotes an ammonium or alkali metal cation. These compounds are suitable as surfactant auxiliaries in oil recovery.

    34.
    发明专利
    未知

    公开(公告)号:NO874426L

    公开(公告)日:1988-04-25

    申请号:NO874426

    申请日:1987-10-23

    Applicant: HOECHST AG

    Abstract: Styrylaryloxy ether sulfonates of the formula in which either R1 denotes styryl and simultaneously R2 and R3 are identical or different and denote hydrogen or styryl, or R1 and R2 are nonidentical and each denote methyl or styryl and simultaneously R3 denotes hydrogen or styryl, x denotes a number from 2 to 20, and M denotes an ammonium or alkali metal cation. These compounds are suitable as surfactant auxiliaries in oil recovery.

    PROCESS FOR THE SIMULTANEOUS PREPARATION OF 2,5-DIOXO-1,2-OXA-PHOSPHOLANES AND (BETA)-HALOGENPROPIONIC ACID HALIDE

    公开(公告)号:CA1086765A

    公开(公告)日:1980-09-30

    申请号:CA274323

    申请日:1977-03-18

    Applicant: HOECHST AG

    Abstract: of the disclosure: 2,5-Dioxo-1,2-oxa-phospholanes of the formula (I) (I) wherein R1 is an organic radical and R2 and R3 each also means organic radicals or hydrogen, are prepared by reacting 2-halogeno-formylethyl-phosphinic acid halides of the formula (II) (II) wherein R1, R2 and R3 are defined as in formula (I) and X means Cl or Br, preferably Cl, with an approximately equimolar quantity of acrylic acid. The compounds (II) may also be produced in the reaction batch and in situ by reacting about equimolar quantities of a dihalogenophosphine of the formula (III) (III) with an .alpha.,.beta.-unsaturated acid (IV) CHR2=CR3-COOH (IV) In the formulae (III) and (IV) R1, R2, R3 and X are defined as indicated above. In the reaction there is formed, in addition to the compounds (I), practically exclusively .beta.-halogenopropionic acid and no free hydrogen halide. The phospholanes (I) are valuable flame retarding agents for plastics, intermediates, for example, for the synthesis of biocidals etc. - 1a

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