PROCESS FOR THE SELECTIVE SYNTHESIS OF SYLILALKYL DISULFIDES DESULFURATING THE CORRESPONDING POLYSULPHIDES WITH NUCLEOPHYLIC REAGENSES

    公开(公告)号:HRP960516B1

    公开(公告)日:2002-04-30

    申请号:HRP960516

    申请日:1996-11-05

    Applicant: DEGUSSA

    Abstract: Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula M CN (IIIA), M 2SO3 (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to be removed from (II); (2) filtering the resultant solid; and (3) purifying (I). In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst.

    PROCESS FOR SELECTIVE SYNTHESIS OF SYLIL-ALKYL-DISULFIDES

    公开(公告)号:HU9603081D0

    公开(公告)日:1996-12-30

    申请号:HU9603081

    申请日:1996-11-06

    Applicant: DEGUSSA

    Abstract: Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula M CN (IIIA), M 2SO3 (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to be removed from (II); (2) filtering the resultant solid; and (3) purifying (I). In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst.

    PROCESS FOR THE PREPARATION OF BIS (SILYL-ALKYL)-DISULFANES

    公开(公告)号:HU9603081A2

    公开(公告)日:1997-10-28

    申请号:HU9603081

    申请日:1996-11-06

    Applicant: DEGUSSA

    Abstract: Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula M CN (IIIA), M 2SO3 (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to be removed from (II); (2) filtering the resultant solid; and (3) purifying (I). In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst.

    METHOD OF SELECTIVELY SYNTHESISING SILYLOALKYLOSULFIDES

    公开(公告)号:PL316746A1

    公开(公告)日:1997-05-12

    申请号:PL31674696

    申请日:1996-10-30

    Applicant: DEGUSSA

    Abstract: Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula M CN (IIIA), M 2SO3 (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to be removed from (II); (2) filtering the resultant solid; and (3) purifying (I). In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst.

    METHOD OF PRODUCTION FOR BIS (SILYALKYL) DISULFIDES

    公开(公告)号:SK143596A3

    公开(公告)日:1997-05-07

    申请号:SK143596

    申请日:1996-11-06

    Applicant: DEGUSSA

    Abstract: Preparation of bis(silylalkyl)disulphanes of formula (R R R SiR )2S2 (I) comprises (1) reacting silylalkyl polysulphide(s) of formula (R R R SiR )2Sn (II) with a nucleophilic compound (III) of formula M CN (IIIA), M 2SO3 (IIIB) or R R R P (IIIC) in an amount equimolar to the number of sulphur atoms to be removed from (II); (2) filtering the resultant solid; and (3) purifying (I). In the formulae, R -R , R -R = 1-8C alkyl and/or alkoxy, H or monovalent aryl, preferably phenyl, toluyl or benzyl; R = divalent 1-8C, preferably 2-4C alkylidene or a group of formula (IV); n = 3-20, preferably 3-10; and M = an alkali cation, optionally substituted ammonium ion or half alkaline earth or zinc ion. Preferably a mixture of (IIIA), (IIIB) and (IIIC) is used. Reaction is carried out in the presence of a solvent for (III) at a temperature between 20 degrees C and the b.pt. of the solvent, especially in a 2-phase system in the presence of a phase transfer catalyst.

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