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    • 2. 发明专利
    • Method for producing organosilane
    • 生产有机硅的方法
    • JP2010037340A
    • 2010-02-18
    • JP2009177297
    • 2009-07-30
    • Evonik Degussa Gmbhエボニック デグサ ゲーエムベーハーEvonik Degussa GmbH
    • KORTH KARSTENKIEFER INGOALIG ALFREDDESCHLER ULRICHDROEGE HELMUTKOENIGSTEIN STEFANSCHWAN STEPHANIE
    • C07F7/18
    • C07F7/1892
    • PROBLEM TO BE SOLVED: To provide a method for producing an organosilane of polysulfide, which method enables a high conversion rate in the case of good selectivity, makes unnecessary the use of a solid alkali metal sulfide hydrate, and allows an alkali metal hydroxide in a sulfuration source material.
      SOLUTION: The method for producing an organosilane represented by general formula I includes reacting a (halogenated organyl)alkoxysilane represented by formula II with a water-containing alkali metal hydrogen sulfide, sulfur, and an alkali metal carbonate in an alcohol. In this method, the molar ratio of the (halogenated organyl)alkoxysilane represented by formula II to the alkali metal hydrogen sulfide is 1:0.40 to 1:0.75 and the molar ratio of the alkali metal hydrogen sulfide to the alkali metal carbonate is 1:0.5 to 1:1.5.
      COPYRIGHT: (C)2010,JPO&INPIT
    • 待解决的问题:为了提供一种生产多硫化物的有机硅烷的方法,该方法能够在选择性好的情况下实现高转化率,不需要使用固体碱金属硫化物水合物,并且允许碱金属 硫化源材料中的氢氧化物。 解决方案:由通式I表示的有机硅烷的制备方法包括使式II表示的(卤代有机基)烷氧基硅烷与含醇的碱金属硫化氢,硫和碱金属碳酸盐在醇中反应。 在该方法中,由式II表示的(卤代有机基)烷氧基硅烷与碱金属硫化氢的摩尔比为1:0.4〜1:0.75,碱金属硫化氢与碱金属碳酸盐的摩尔比为1: 0.5至1:1.5。 版权所有(C)2010,JPO&INPIT
    • 3. 发明专利
    • AT523516T
    • 2011-09-15
    • AT09166242
    • 2009-07-23
    • EVONIK DEGUSSA GMBH
    • KORTH KARSTENKIEFER INGOALIG ALFREDDESCHLER ULRICHDROEGE HELMUTKOENIGSTEIN STEFANSCHWAN STEPHANIE
    • C07F7/18
    • Preparation of organosilanes (I), comprises reacting (halogenoorganyl)alkoxysilane (II) with aqueous alkaline hydrogen sulfide, sulfur and alkali-carbonate in alcohol, where the molar ratio of (halogenoorganyl)alkoxysilane to alkaline hydrogen sulfide is 1:0.4 to 1:0.75 and the molar ratio of alkali-carbonate to alkaline hydrogen sulfide is 1:0.5 to 1:1.5. Preparation of organosilanes of formula ([((R) 2)(R 1>-O)Si-R 2>)] 2-S m) (I), comprises reacting (halogenoorganyl)alkoxysilane of formula ([((R) 2)(R 1>-O)Si-R 2>)]-X) (II) with aqueous alkaline hydrogen sulfide, sulfur and alkali-carbonate in alcohol, where the molar ratio of (halogenoorganyl)alkoxysilane to alkaline hydrogen sulfide is 1:0.4 to 1:0.75 and the molar ratio of alkali-carbonate to alkaline hydrogen sulfide is 1:0.5 to 1:1.5. R : 1-8C alkyl, 1-8C alkenyl, 1-8C aryl, 1-8C aralkyl or OR 1>; R 1>H, 1-24C monovalent alkyl or alkenyl, aryl, aralkyl, alkyl ether (-(C(R 3>) 2) y 1>-O-R 4>) or alkyl polyether (-C(R 3>) 2O) y 2>-R 4> or -(C(R 3>) 2-C(R 3>) 2-O) y 2>-R 4>); y 1>1-20; y 2>2-20; R 3>H or alkyl; R 4>optionally saturated, aromatic or mixed aliphatic/aromatic monovalent 1-30C hydrocarbon; R 2>optionally saturated aliphatic, aromatic or mixed aliphatic/aromatic divalent 1-30C hydrocarbon, which is optionally substituted with F, Cl, Br, I, SH, NH 2 or NHR 1>; m : average sulfur chain length of 1.5-4.5; and X : Cl, Br, F or I.
    • 4. 发明专利
    • AT423125T
    • 2009-03-15
    • AT06117189
    • 2006-07-14
    • EVONIK DEGUSSA GMBH
    • FRINGS ALBERTJANSSENS LOUISLOTTER STEFANDESCHLER ULRICHALIG ALFRED
    • C07F7/18
    • Preparation of organosilicon compound (I) comprises reacting halogenalkoxysilane (II) with a dry polysulfide (III) dry sulfide (IV) and optionally a sulfur in an organic solvent; removing the mixture containing (I) and the solid material with water containing at least a buffer from the organic solvent and separating the binding phase. Preparation of organosilicon compound (I) of formula ((R 1>R 2>R 3>SiR 4>) 2S x) comprises reacting halogenalkoxysilane compound (II) of formula (R 1>R 2>R 3>SiR 4>X) with a dry polysulfide compound (III) of formula (M 2S z) dry sulfide (IV) of formula (M 2S) and optionally a sulfur in an organic solvent; removing the mixture containing (I) and the solid material (MX) with water containing at least a buffer from the organic solvent and separating the binding phase. R 1>-R 3>alkyl, alkoxy (preferred) or aryl; R 4>1-30C-aliphatic/aromatic hydrocarbon; x : greater than 1; X : halogen atom; M : alkali cation, an ammonium or semi alkaline earth or zinc cation; and z : 2-8.
    • 7. 发明专利
    • DE102008035623A1
    • 2010-02-04
    • DE102008035623
    • 2008-07-31
    • EVONIK DEGUSSA GMBH
    • KORTH KARSTENKIEFER INGOALIG ALFREDDESCHLER ULRICHDROEGE HELMUTKOENIGSTEIN STEFANSCHWAN STEPHANIE
    • C07F7/02C07F7/18
    • Preparation of organosilanes (I), comprises reacting (halogenoorganyl)alkoxysilane (II) with aqueous alkaline hydrogen sulfide, sulfur and alkali-carbonate in alcohol, where the molar ratio of (halogenoorganyl)alkoxysilane to alkaline hydrogen sulfide is 1:0.4 to 1:0.75 and the molar ratio of alkali-carbonate to alkaline hydrogen sulfide is 1:0.5 to 1:1.5. Preparation of organosilanes of formula ([((R) 2)(R 1>-O)Si-R 2>)] 2-S m) (I), comprises reacting (halogenoorganyl)alkoxysilane of formula ([((R) 2)(R 1>-O)Si-R 2>)]-X) (II) with aqueous alkaline hydrogen sulfide, sulfur and alkali-carbonate in alcohol, where the molar ratio of (halogenoorganyl)alkoxysilane to alkaline hydrogen sulfide is 1:0.4 to 1:0.75 and the molar ratio of alkali-carbonate to alkaline hydrogen sulfide is 1:0.5 to 1:1.5. R : 1-8C alkyl, 1-8C alkenyl, 1-8C aryl, 1-8C aralkyl or OR 1>; R 1>H, 1-24C monovalent alkyl or alkenyl, aryl, aralkyl, alkyl ether (-(C(R 3>) 2) y 1>-O-R 4>) or alkyl polyether (-C(R 3>) 2O) y 2>-R 4> or -(C(R 3>) 2-C(R 3>) 2-O) y 2>-R 4>); y 1>1-20; y 2>2-20; R 3>H or alkyl; R 4>optionally saturated, aromatic or mixed aliphatic/aromatic monovalent 1-30C hydrocarbon; R 2>optionally saturated aliphatic, aromatic or mixed aliphatic/aromatic divalent 1-30C hydrocarbon, which is optionally substituted with F, Cl, Br, I, SH, NH 2 or NHR 1>; m : average sulfur chain length of 1.5-4.5; and X : Cl, Br, F or I.
    • 8. 发明专利
    • DE502006002874D1
    • 2009-04-02
    • DE502006002874
    • 2006-07-14
    • EVONIK DEGUSSA GMBH
    • FRINGS ALBERTJANSSENS LOUISLOTTER STEFANDESCHLER ULRICHALIG ALFRED
    • C07F7/18
    • Preparation of organosilicon compound (I) comprises reacting halogenalkoxysilane (II) with a dry polysulfide (III) dry sulfide (IV) and optionally a sulfur in an organic solvent; removing the mixture containing (I) and the solid material with water containing at least a buffer from the organic solvent and separating the binding phase. Preparation of organosilicon compound (I) of formula ((R 1>R 2>R 3>SiR 4>) 2S x) comprises reacting halogenalkoxysilane compound (II) of formula (R 1>R 2>R 3>SiR 4>X) with a dry polysulfide compound (III) of formula (M 2S z) dry sulfide (IV) of formula (M 2S) and optionally a sulfur in an organic solvent; removing the mixture containing (I) and the solid material (MX) with water containing at least a buffer from the organic solvent and separating the binding phase. R 1>-R 3>alkyl, alkoxy (preferred) or aryl; R 4>1-30C-aliphatic/aromatic hydrocarbon; x : greater than 1; X : halogen atom; M : alkali cation, an ammonium or semi alkaline earth or zinc cation; and z : 2-8.
    • 10. 发明专利
    • BRPI0902472A2
    • 2010-04-20
    • BRPI0902472
    • 2009-07-22
    • EVONIK DEGUSSA GMBH
    • KORTH KARSTENKIEFER INGOALIG ALFREDDESCHLER ULRICHDROEGE HELMUTKOENIGSTEIN STEFANSCHWAN STEPHANIE
    • C07F7/18
    • Preparation of organosilanes (I), comprises reacting (halogenoorganyl)alkoxysilane (II) with aqueous alkaline hydrogen sulfide, sulfur and alkali-carbonate in alcohol, where the molar ratio of (halogenoorganyl)alkoxysilane to alkaline hydrogen sulfide is 1:0.4 to 1:0.75 and the molar ratio of alkali-carbonate to alkaline hydrogen sulfide is 1:0.5 to 1:1.5. Preparation of organosilanes of formula ([((R) 2)(R 1>-O)Si-R 2>)] 2-S m) (I), comprises reacting (halogenoorganyl)alkoxysilane of formula ([((R) 2)(R 1>-O)Si-R 2>)]-X) (II) with aqueous alkaline hydrogen sulfide, sulfur and alkali-carbonate in alcohol, where the molar ratio of (halogenoorganyl)alkoxysilane to alkaline hydrogen sulfide is 1:0.4 to 1:0.75 and the molar ratio of alkali-carbonate to alkaline hydrogen sulfide is 1:0.5 to 1:1.5. R : 1-8C alkyl, 1-8C alkenyl, 1-8C aryl, 1-8C aralkyl or OR 1>; R 1>H, 1-24C monovalent alkyl or alkenyl, aryl, aralkyl, alkyl ether (-(C(R 3>) 2) y 1>-O-R 4>) or alkyl polyether (-C(R 3>) 2O) y 2>-R 4> or -(C(R 3>) 2-C(R 3>) 2-O) y 2>-R 4>); y 1>1-20; y 2>2-20; R 3>H or alkyl; R 4>optionally saturated, aromatic or mixed aliphatic/aromatic monovalent 1-30C hydrocarbon; R 2>optionally saturated aliphatic, aromatic or mixed aliphatic/aromatic divalent 1-30C hydrocarbon, which is optionally substituted with F, Cl, Br, I, SH, NH 2 or NHR 1>; m : average sulfur chain length of 1.5-4.5; and X : Cl, Br, F or I.