Method for preparing halosilane compounds
US-11731992-B2 · Aug 22, 2023 · US
US2023141781A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2023141781-A1 |
| Application number | US-202017917562-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 23, 2020 |
| Priority date | Apr 23, 2020 |
| Publication date | May 11, 2023 |
| Grant date | — |
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A process for dehydrogenating and methylating silanes. The process includes providing methyl chloride that is reacted with a silane selected from the group consisting of SiH 4 , H 2 SiMe 2 , H 2 SiMeCl, H 3 SiMe, H 3 SiCl and HSiMe 2 Cl, in the presence of at least one ammonium and/or phosphonium salt at a temperature in the range of 70-350° C.
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1 - 7 . (canceled) 8 . A process for dehydrogenating and methylating silanes, comprising: providing methyl chloride that is reacted with a silane selected from the group consisting of SiH 4 , H 2 SiMe 2 , H 2 SiMeCl, H 3 SiMe, H 3 SiCl and HSiMe 2 Cl, in the presence of at least one ammonium and/or phosphonium salt at a temperature in the range of 70-350° C. 9 . The process as claimed in claim 8 , wherein the temperature is in a range of 100-350° C. 10 . The process of claim 8 , wherein the molar ratio of silane to methyl chloride is in a range of 1:1 to 1:10. 11 . The process of claim 8 , wherein the molar ratio of catalyst to silane is in a range of 0.01:1 to 0.2:1. 12 . The process of claim 8 , wherein the ammonium and/or phosphonium salt is selected from the group consisting of quaternary ammonium halides [R 4 N]X, quaternary phosphonium halides [R 4 P]X and tertiary ammonium halides [R 3 NH]X, wherein in each case: X=Cl, Br or I, and R=independently selected from the group consisting of (i) C 1 -C 12 -alkyl group, (ii) C 6 -C 14 -aryl group substituted by C 1 -C 6 -alkyl, and (iii) phenyl group. 13 . The process of claim 12 , wherein the ammonium and/or phosphonium salt is selected from the group consisting of [n-Bu 4 N]Cl, [Et 4 N]Cl, [Ph 4 P]Cl and [n-Bu 4 P]Cl. 14 . The process of claim 8 , wherein the process is conducted continuously or batchwise.
Aromatic phosphonium compounds (P-C aromatic linkage) · CPC title
by reactions involving both Si-C and Si-halogen linkages, the Si-C and Si-halogen linkages can be to the same or to different Si atoms, e.g. redistribution reactions · CPC title
Preparation thereof from {optionally substituted} halogenated silanes and hydrocarbons {hydrosilylation reactions} · CPC title
Acyclic saturated phosphonium compounds · CPC title
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