GB609507A - Improved process for the production of alkyl silicon halides - Google Patents
Improved process for the production of alkyl silicon halidesInfo
- Publication number
- GB609507A GB609507A GB960/46A GB96046A GB609507A GB 609507 A GB609507 A GB 609507A GB 960/46 A GB960/46 A GB 960/46A GB 96046 A GB96046 A GB 96046A GB 609507 A GB609507 A GB 609507A
- Authority
- GB
- United Kingdom
- Prior art keywords
- silicon
- methyl
- ferrosilicon
- chloride
- zirconium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229910052710 silicon Inorganic materials 0.000 title abstract 7
- 239000010703 silicon Substances 0.000 title abstract 7
- -1 alkyl silicon halides Chemical class 0.000 title abstract 6
- 229910000519 Ferrosilicon Inorganic materials 0.000 abstract 8
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 abstract 6
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 abstract 5
- 150000001350 alkyl halides Chemical class 0.000 abstract 5
- 239000005049 silicon tetrachloride Substances 0.000 abstract 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 4
- 229940050176 methyl chloride Drugs 0.000 abstract 4
- PPDADIYYMSXQJK-UHFFFAOYSA-N trichlorosilicon Chemical compound Cl[Si](Cl)Cl PPDADIYYMSXQJK-UHFFFAOYSA-N 0.000 abstract 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 3
- 229910045601 alloy Inorganic materials 0.000 abstract 3
- 239000000956 alloy Substances 0.000 abstract 3
- 239000007795 chemical reaction product Substances 0.000 abstract 3
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 abstract 3
- 229960003750 ethyl chloride Drugs 0.000 abstract 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 3
- 229910000039 hydrogen halide Inorganic materials 0.000 abstract 3
- 239000012433 hydrogen halide Substances 0.000 abstract 3
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- ZOYFEXPFPVDYIS-UHFFFAOYSA-N trichloro(ethyl)silane Chemical compound CC[Si](Cl)(Cl)Cl ZOYFEXPFPVDYIS-UHFFFAOYSA-N 0.000 abstract 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- XEQZXHPGUAHHPE-UHFFFAOYSA-N [Mn].[Ca].[Si] Chemical compound [Mn].[Ca].[Si] XEQZXHPGUAHHPE-UHFFFAOYSA-N 0.000 abstract 2
- QGIJYACZZPNOQJ-UHFFFAOYSA-N [Si].[Zr].[Mn] Chemical compound [Si].[Zr].[Mn] QGIJYACZZPNOQJ-UHFFFAOYSA-N 0.000 abstract 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 abstract 2
- UVGLBOPDEUYYCS-UHFFFAOYSA-N silicon zirconium Chemical compound [Si].[Zr] UVGLBOPDEUYYCS-UHFFFAOYSA-N 0.000 abstract 2
- 229910000789 Aluminium-silicon alloy Inorganic materials 0.000 abstract 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 229910000676 Si alloy Inorganic materials 0.000 abstract 1
- UGACIEPFGXRWCH-UHFFFAOYSA-N [Si].[Ti] Chemical compound [Si].[Ti] UGACIEPFGXRWCH-UHFFFAOYSA-N 0.000 abstract 1
- OSMSIOKMMFKNIL-UHFFFAOYSA-N calcium;silicon Chemical compound [Ca]=[Si] OSMSIOKMMFKNIL-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract 1
- XKBAVCUSVIEVHR-UHFFFAOYSA-N dibromo(methyl)silane Chemical compound C[SiH](Br)Br XKBAVCUSVIEVHR-UHFFFAOYSA-N 0.000 abstract 1
- VJIYRPVGAZXYBD-UHFFFAOYSA-N dibromosilane Chemical compound Br[SiH2]Br VJIYRPVGAZXYBD-UHFFFAOYSA-N 0.000 abstract 1
- PFMKUUJQLUQKHT-UHFFFAOYSA-N dichloro(ethyl)silicon Chemical compound CC[Si](Cl)Cl PFMKUUJQLUQKHT-UHFFFAOYSA-N 0.000 abstract 1
- KTQYJQFGNYHXMB-UHFFFAOYSA-N dichloro(methyl)silicon Chemical compound C[Si](Cl)Cl KTQYJQFGNYHXMB-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 238000007689 inspection Methods 0.000 abstract 1
- XWHPIFXRKKHEKR-UHFFFAOYSA-N iron silicon Chemical compound [Si].[Fe] XWHPIFXRKKHEKR-UHFFFAOYSA-N 0.000 abstract 1
- ULYZAYCEDJDHCC-UHFFFAOYSA-N isopropyl chloride Chemical compound CC(C)Cl ULYZAYCEDJDHCC-UHFFFAOYSA-N 0.000 abstract 1
- 229940102396 methyl bromide Drugs 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000005048 methyldichlorosilane Substances 0.000 abstract 1
- AIFMYMZGQVTROK-UHFFFAOYSA-N silicon tetrabromide Chemical compound Br[Si](Br)(Br)Br AIFMYMZGQVTROK-UHFFFAOYSA-N 0.000 abstract 1
- KBSUPJLTDMARAI-UHFFFAOYSA-N tribromo(methyl)silane Chemical compound C[Si](Br)(Br)Br KBSUPJLTDMARAI-UHFFFAOYSA-N 0.000 abstract 1
- IBOKZQNMFSHYNQ-UHFFFAOYSA-N tribromosilane Chemical compound Br[SiH](Br)Br IBOKZQNMFSHYNQ-UHFFFAOYSA-N 0.000 abstract 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005052 trichlorosilane Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
- C07F7/16—Preparation thereof from silicon and halogenated hydrocarbons direct synthesis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Alkyl silicon halides are prepared by bringing a vapour mixture of an alkyl halide, e.g. one which contains less than four carbon atoms in the molecule such as methyl or ethyl chloride, and a hydrogen halide, or a vapour mixture of an olefine and more than its molecular equivalent of a hydrogen halide, into contact with silicon at a reaction temperature between 250 DEG and 550 DEG C., but preferably between 300 DEG and 450 DEG C. The vapour mixture may comprise one part by volume of an alkyl halide and from 0.5 to 20 parts of a hydrogen halide. The silicon may be employed in the form of an alloy, e.g. ferrosilicon or calcium-manganese-silicon, manganese-zirconium-silicon, titanium-silicon, zirconium-silicon, or calcium-titanium-aluminium-zirconium-boron-iron-silicon alloys may be used. A substantial portion of the reaction products, e.g. from 0.5 to 0.8 of the reaction products, may be recirculated into contact with the silicon or an alloy thereof, and the remainder of the reaction products withdrawn from the system. The reaction is usually carried out at atmospheric pressure, but lower or higher pressures may be employed, and a diluent may be employed, e.g. carbon dioxide, carbon monoxide, silicon tetrachloride or trichlorosilane. The reaction may be effected in an intermittent or continuous way, or in a batchwise manner, e.g. in a bomb or autoclave. The preparation of methyl silicon trichloride is given by contacting methyl chloride vapours with heated ferrosilicon. In examples (1) to (4), methyl silicon trichloride, methyl-dichlorosilane, silicochloroform and silicon tetrachloride are obtained by contacting methyl chloride and hydrogen chloride vapours with heated ferrosilicon and ethyl silicon trichloride, silicon tetrachloride and silicochloroform by contacting ethyl chloride and hydrogen chloride with heated ferrosilicon. In example (5), ethyl silicon trichloride, silicon tetrachloride and silicochloroform are obtained by passing hydrogen chloride and ethylene over heated ferrosilicon. Specifications 575,667, 575,668, 575,673 and 575,674 are referred to. The Specification as open to inspection under Sect. 91 refers to the preparation of alkyl silicon halides by reacting alkyl halides, or components of alkyl halides which react readily to form alkyl halides, with silicon or an alloy thereof at an elevated temperature. In examples, methyl bromide is reacted with ferrosilicon to yield methyl silicon tribromide, silicon tetrabromide, dibromo- and tribromosilane and methyldibromosilane, ethyl chloride is reacted with heated ferrosilicon to yield ethyl silicon trichloride, silicon tetrachloride, silicochloroform and ethyldichlorosilane, isopropyl chloride is reacted with heated ferrosilicon to yield isopropyl-dichlorosilone, and methyl silicon trichloride is prepared by passing methyl chloride vapour over calcium silicon, calcium-manganese - silicon, manganese - zirconium - silicon, iron - silicon, zirconium - calcium - titanium-aluminium-boron-iron-silicon, zirconium-silicon, or titanium-aluminium-silicon alloy. This subject-matter does not p appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US609507XA | 1945-01-15 | 1945-01-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB609507A true GB609507A (en) | 1948-10-01 |
Family
ID=22032753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB960/46A Expired GB609507A (en) | 1945-01-15 | 1946-01-10 | Improved process for the production of alkyl silicon halides |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE870257C (en) |
GB (1) | GB609507A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE899352C (en) * | 1949-01-27 | 1953-12-10 | Wacker Chemie Gmbh | Process for the preparation of methyl- or phenylhalosilanes |
US2672475A (en) * | 1952-12-01 | 1954-03-16 | Dow Corning | Process for preparing alkyl trichlorosilanes |
DE970283C (en) * | 1950-05-19 | 1958-09-04 | Bayer Ag | Process for the preparation of alkyl or aryl halosilanes |
DE970341C (en) * | 1950-11-29 | 1958-09-11 | Goldschmidt Ag Th | Process for the preparation of alkylhalosilanes |
-
1946
- 1946-01-10 GB GB960/46A patent/GB609507A/en not_active Expired
-
1950
- 1950-09-29 DE DED6425A patent/DE870257C/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE899352C (en) * | 1949-01-27 | 1953-12-10 | Wacker Chemie Gmbh | Process for the preparation of methyl- or phenylhalosilanes |
DE970283C (en) * | 1950-05-19 | 1958-09-04 | Bayer Ag | Process for the preparation of alkyl or aryl halosilanes |
DE970341C (en) * | 1950-11-29 | 1958-09-11 | Goldschmidt Ag Th | Process for the preparation of alkylhalosilanes |
US2672475A (en) * | 1952-12-01 | 1954-03-16 | Dow Corning | Process for preparing alkyl trichlorosilanes |
Also Published As
Publication number | Publication date |
---|---|
DE870257C (en) | 1953-03-12 |
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