1.
    发明专利
    未知

    公开(公告)号:DE502004000376D1

    公开(公告)日:2006-05-11

    申请号:DE502004000376

    申请日:2004-10-19

    Applicant: DEGUSSA

    Abstract: Production of mercaptoorganyl alkoxysilanes comprises reacting an alkali metal hydrogen sulfide with a mixture of haloorganyl alkoxysilane and haloorganyl halosilane in an alcohol under pressure in a sealed vessel in the absence of oxygen.

    2.
    发明专利
    未知

    公开(公告)号:DE502004000168D1

    公开(公告)日:2006-01-12

    申请号:DE502004000168

    申请日:2004-06-09

    Applicant: DEGUSSA

    Abstract: New organosilicon compounds (I) are mercapto-, thiocyanato- and mono- and polysulfanyl-(ar)alkyl- and (alk)aryl-silanes, in which (each) silicon atom has 1-3 long-chain alk(en)oxy-, aryloxy, aralkoxy or tri(alk(en)yl, aralkyl or aryl)-siloxy substituents and 0-2 alkyl substituents, and mixtures of these. New organosilicon compounds are mercapto-, thiocyanato- and mono- and polysulfanyl-(ar)alkyl- and (alk)aryl-silanes of formula (I) and mixtures are claimed. [Image] R : R'O or 1-12 C alkyl; R' : 12-24 C monovalent alkyl or alkenyl, aryl, aralkyl or R''' 3Si; R''' : 1-30 C alkyl or alkenyl, aralkyl or aryl; R'' : (un)saturated aliphatic, aromatic or mixed aliphatic/aromatic divalent 1-30 C hydrocarbon group; and X : SH or SCN with n = 1 and m = 1, or S with n = 2 and m = 1-14. Independent claims are also included for the following: (1) preparation of (I); (2) rubber mixes containing rubber, filler, optionally other ancillaries and also compound(s) (I).

    3.
    发明专利
    未知

    公开(公告)号:DE50200179D1

    公开(公告)日:2004-02-05

    申请号:DE50200179

    申请日:2002-01-11

    Applicant: DEGUSSA

    Abstract: Production of 3-functionalized propyl silanes (I) by reacting allylic compounds (II) with silanes (III) at 0-200 degrees C and 0.8-25 bar in the presence of a platinum catalyst comprises using a (III):(II) molar ratio of 3-100. Production of 3-functionalized propyl silanes (I) by reacting allylic compounds of formula (II) with silanes of formula (III) at 0-200 degrees C and 0.8-25 bar in the presence of a platinum catalyst comprises using a (III):(II) molar ratio of 3-100:1 H2C=CH-CH2X (II) R R R SiH (III) X = Cl, Br, I, F, CN, SCN, SH, SR, OH, NRR or OR; R, R = 1-6C alkyl or 3-7C alkyl (sic); and R -R = H, halogen, 1-6C alkyl, 1-6C haloalkyl, 3-6C allyl (sic), 1-4C alkoxy, phenyl, aryl or aralkyl.

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