Process for preparing organosilanes

Process for preparing organosilanes

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...

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Hauptverfasser: DESCHLER ULRICH, SCHWAN STEPHANIE, KOENIGSTEIN STEFAN, KORTH KARSTEN, KIEFER INGO, DROEGE HELMUT, ALIG ALFRED
Format: Patent
Sprache:chi ; eng
Schlagworte:
ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
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Zusammenfassung: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(