IL147949A - Process for producing converted silanes profile in position 3 - Google Patents
Process for producing converted silanes profile in position 3Info
- Publication number
- IL147949A IL147949A IL14794900A IL14794900A IL147949A IL 147949 A IL147949 A IL 147949A IL 14794900 A IL14794900 A IL 14794900A IL 14794900 A IL14794900 A IL 14794900A IL 147949 A IL147949 A IL 147949A
- Authority
- IL
- Israel
- Prior art keywords
- trichlorosilane
- process according
- catalyst
- reactor
- component
- Prior art date
Links
- UIDUKLCLJMXFEO-UHFFFAOYSA-N propylsilane Chemical class CCC[SiH3] UIDUKLCLJMXFEO-UHFFFAOYSA-N 0.000 title claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 238000000034 method Methods 0.000 title claims description 27
- 239000003054 catalyst Substances 0.000 claims abstract description 30
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 18
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 9
- 150000004756 silanes Chemical class 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 5
- 150000002367 halogens Chemical class 0.000 claims abstract description 5
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 4
- 125000003118 aryl group Chemical group 0.000 claims abstract description 4
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 4
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 3
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 3
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 3
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 claims description 59
- 239000005052 trichlorosilane Substances 0.000 claims description 56
- 239000000203 mixture Substances 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 26
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 21
- 229910000077 silane Inorganic materials 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- -1 propene compound Chemical class 0.000 claims description 12
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 12
- 150000002431 hydrogen Chemical class 0.000 claims description 10
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 claims description 4
- 239000005046 Chlorosilane Substances 0.000 claims description 3
- 238000007259 addition reaction Methods 0.000 claims description 3
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 claims description 3
- 230000006735 deficit Effects 0.000 claims description 2
- 125000000746 allylic group Chemical group 0.000 abstract 2
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 62
- OOXSLJBUMMHDKW-UHFFFAOYSA-N trichloro(3-chloropropyl)silane Chemical compound ClCCC[Si](Cl)(Cl)Cl OOXSLJBUMMHDKW-UHFFFAOYSA-N 0.000 description 45
- 239000005053 propyltrichlorosilane Substances 0.000 description 28
- DOEHJNBEOVLHGL-UHFFFAOYSA-N trichloro(propyl)silane Chemical compound CCC[Si](Cl)(Cl)Cl DOEHJNBEOVLHGL-UHFFFAOYSA-N 0.000 description 28
- 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 description 27
- 239000005049 silicon tetrachloride Substances 0.000 description 27
- 239000000047 product Substances 0.000 description 21
- 239000000126 substance Substances 0.000 description 14
- 238000010517 secondary reaction Methods 0.000 description 4
- DTOOTUYZFDDTBD-UHFFFAOYSA-N 3-chloropropylsilane Chemical class [SiH3]CCCCl DTOOTUYZFDDTBD-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910004721 HSiCl3 Inorganic materials 0.000 description 3
- 238000006459 hydrosilylation reaction Methods 0.000 description 3
- 150000003058 platinum compounds Chemical class 0.000 description 3
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 2
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 101000623895 Bos taurus Mucin-15 Proteins 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229910002621 H2PtCl6 Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007210 heterogeneous catalysis Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 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
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/0825—Preparations of compounds not comprising Si-Si or Si-cyano linkages
- C07F7/0827—Syntheses with formation of a Si-C bond
- C07F7/0829—Hydrosilylation reactions
-
- 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
- C07F7/14—Preparation thereof from optionally substituted halogenated silanes and hydrocarbons hydrosilylation reactions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Silicon Polymers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10104966A DE10104966A1 (de) | 2001-02-03 | 2001-02-03 | Verfahren zur Herstellung von in 3-Stellung funktionalisierten Propylsilanen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL147949A true IL147949A (en) | 2004-12-15 |
Family
ID=7672785
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL14794900A IL147949A (en) | 2001-02-03 | 2000-01-31 | Process for producing converted silanes profile in position 3 |
| IL14794902A IL147949A0 (en) | 2001-02-03 | 2002-01-31 | Process for the production of propyl silanes functionalised in 3-position |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL14794902A IL147949A0 (en) | 2001-02-03 | 2002-01-31 | Process for the production of propyl silanes functionalised in 3-position |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6472549B1 (pl) |
| EP (1) | EP1229039B1 (pl) |
| JP (1) | JP4338348B2 (pl) |
| KR (1) | KR100795317B1 (pl) |
| CN (1) | CN1217949C (pl) |
| AT (1) | ATE257158T1 (pl) |
| BR (1) | BR0200278A (pl) |
| CZ (1) | CZ2002388A3 (pl) |
| DE (2) | DE10104966A1 (pl) |
| ES (1) | ES2213712T3 (pl) |
| HU (1) | HUP0200377A3 (pl) |
| IL (2) | IL147949A (pl) |
| MX (1) | MXPA02001186A (pl) |
| MY (1) | MY120872A (pl) |
| PL (1) | PL203230B1 (pl) |
| RU (1) | RU2275375C2 (pl) |
| UA (1) | UA76698C2 (pl) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020008011A1 (en) * | 2000-03-28 | 2002-01-24 | Raymund Sonnenschein | Method for the preparation of propylsilanes functionalized in the 3 position |
| DE10153795A1 (de) * | 2001-10-31 | 2003-05-22 | Degussa | Verfahren zur Herstellung von in 3-Stellung funktionalisierten Propylsilanen |
| US20040092759A1 (en) * | 2002-11-12 | 2004-05-13 | Westmeyer Mark D. | Process for making haloalkylalkoxysilanes |
| CN100378111C (zh) * | 2005-07-01 | 2008-04-02 | 中国科学院上海有机化学研究所 | 含碳氧醚键有机硅化合物、合成方法及其应用 |
| RU2320667C1 (ru) * | 2007-01-09 | 2008-03-27 | Открытое акционерное общество "Химпром" | Способ получения 3-хлорпропилсилана |
| EP2324039B1 (en) * | 2008-07-01 | 2013-05-29 | Momentive Performance Materials Inc. | Hydrosilylation process for gaseous unsaturated hydrocarbons |
| DE102010001531A1 (de) | 2010-02-03 | 2011-08-04 | Evonik Goldschmidt GmbH, 45127 | Neuartige organomodifizierte Siloxane mit primären Aminofunktionen, neuartige organomodifizierte Siloxane mit quaternären Ammoniumfunktionen und das Verfahren zu deren Herstellung |
| CN105541895B (zh) * | 2015-12-25 | 2017-12-29 | 淄博市临淄齐泉工贸有限公司 | 一种γ‑氯丙基三氯硅烷的生产方法 |
| CN105837612B (zh) * | 2016-01-27 | 2019-06-11 | 浙江新安化工集团股份有限公司 | 一种γ-氯丙基三氯硅烷的生产方法及生产系统 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU160183A (pl) * | ||||
| US2637738A (en) | 1949-09-17 | 1953-05-05 | Union Carbide & Carbon Corp | Reaction of silanes with aliphatic unsaturated compounds |
| GB923710A (en) | 1960-11-07 | 1963-04-18 | Ici Ltd | Production of organosilicon compounds |
| DE1165028B (de) | 1962-11-14 | 1964-03-12 | Goldschmidt Ag Th | Verfahren zur Herstellung von siliciumhaltigen Kohlenwasserstoffen durch Addition von Hydrogensilanen an ungesaettigte Kohlenwasserstoffe |
| DE2851456C2 (de) | 1978-11-28 | 1982-09-23 | Wacker-Chemie GmbH, 8000 München | Verfahren zur Herstellung von Organosiliciumverbindungen |
| JPS55145693A (en) * | 1979-05-02 | 1980-11-13 | Chisso Corp | Preparation of 3-chloropropyltrichlorosilane |
| DE3000768A1 (de) | 1980-01-10 | 1981-07-16 | Wacker-Chemie GmbH, 8000 München | Verfahren zum anlagern von si-gebundenem wasserstoff an aliphatische mehrfachbindung |
| US4292433A (en) * | 1980-10-31 | 1981-09-29 | Chisso Corporation | Method for producing 3-chloropropyltrichlorosilane |
| DE3404703A1 (de) * | 1984-02-10 | 1985-09-05 | Degussa Ag, 6000 Frankfurt | Verfahren zur herstellung von 3-chlorpropyltrichlorsilan |
| DE4119994A1 (de) * | 1991-06-18 | 1992-12-24 | Huels Chemische Werke Ag | Verfahren zur herstellung von 3-chlorpropylsilanen |
| DE19825793C1 (de) * | 1998-06-10 | 2000-01-05 | Degussa | Verfahren zur Herstellung von in 3-Stellung funktionalisierten Organosilanen |
| DE19857223C5 (de) * | 1998-12-11 | 2010-02-04 | Evonik Degussa Gmbh | Verfahren zur Herstellung von Propylsilanen |
-
2000
- 2000-01-31 IL IL14794900A patent/IL147949A/en not_active IP Right Cessation
-
2001
- 2001-02-03 DE DE10104966A patent/DE10104966A1/de not_active Withdrawn
-
2002
- 2002-01-11 EP EP02000682A patent/EP1229039B1/de not_active Expired - Lifetime
- 2002-01-11 ES ES02000682T patent/ES2213712T3/es not_active Expired - Lifetime
- 2002-01-11 AT AT02000682T patent/ATE257158T1/de not_active IP Right Cessation
- 2002-01-11 DE DE50200179T patent/DE50200179D1/de not_active Expired - Lifetime
- 2002-01-30 MY MYPI20020330A patent/MY120872A/en unknown
- 2002-01-31 IL IL14794902A patent/IL147949A0/xx unknown
- 2002-01-31 JP JP2002024159A patent/JP4338348B2/ja not_active Expired - Lifetime
- 2002-01-31 CZ CZ2002388A patent/CZ2002388A3/cs unknown
- 2002-02-01 BR BR0200278-7A patent/BR0200278A/pt not_active Application Discontinuation
- 2002-02-01 PL PL351985A patent/PL203230B1/pl unknown
- 2002-02-01 UA UA2002020850A patent/UA76698C2/uk unknown
- 2002-02-01 HU HU0200377A patent/HUP0200377A3/hu not_active Application Discontinuation
- 2002-02-01 US US10/060,287 patent/US6472549B1/en not_active Expired - Lifetime
- 2002-02-01 MX MXPA02001186A patent/MXPA02001186A/es active IP Right Grant
- 2002-02-01 CN CN021032548A patent/CN1217949C/zh not_active Expired - Lifetime
- 2002-02-01 KR KR1020020005897A patent/KR100795317B1/ko not_active Expired - Fee Related
- 2002-02-04 RU RU2002102763/04A patent/RU2275375C2/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002302495A (ja) | 2002-10-18 |
| HUP0200377A3 (en) | 2003-07-28 |
| KR100795317B1 (ko) | 2008-01-21 |
| CZ2002388A3 (cs) | 2002-09-11 |
| IL147949A0 (en) | 2002-08-14 |
| ATE257158T1 (de) | 2004-01-15 |
| KR20020064867A (ko) | 2002-08-10 |
| HU0200377D0 (en) | 2002-03-28 |
| EP1229039A1 (de) | 2002-08-07 |
| MY120872A (en) | 2005-11-30 |
| US6472549B1 (en) | 2002-10-29 |
| CN1217949C (zh) | 2005-09-07 |
| DE10104966A1 (de) | 2002-08-08 |
| RU2275375C2 (ru) | 2006-04-27 |
| PL203230B1 (pl) | 2009-09-30 |
| JP4338348B2 (ja) | 2009-10-07 |
| BR0200278A (pt) | 2003-04-29 |
| ES2213712T3 (es) | 2004-09-01 |
| DE50200179D1 (de) | 2004-02-05 |
| HUP0200377A2 (hu) | 2003-01-28 |
| UA76698C2 (en) | 2006-09-15 |
| MXPA02001186A (es) | 2004-05-27 |
| EP1229039B1 (de) | 2004-01-02 |
| CN1369497A (zh) | 2002-09-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR940010290B1 (ko) | 비스실릴메탄 및 그들의 제조방법 | |
| US6472549B1 (en) | Process for the production of propyl silanes functionalized in 3-position | |
| JPH07101962A (ja) | アルケニルクロロシラン及びその製造方法 | |
| JPH05255355A (ja) | ビスシリルアルカンの製造方法 | |
| US20070060765A1 (en) | Organochlorosilane and dipodal silane compounds | |
| US6242630B1 (en) | Process for the continuous preparation of 3-halopropylorganosilanes | |
| US20090036702A1 (en) | Production of organosilanes in the presence of iridium-catalysts and cocatalysts | |
| KR20110107349A (ko) | 오가노할로하이드로실란의 제조 공정 | |
| EP2262817B1 (en) | Process for the preparation of haloalkylalkoxysilancs and haloalkylhalosilanes | |
| JP4527351B2 (ja) | 改善されたオルガノシラン製造方法 | |
| US20020008011A1 (en) | Method for the preparation of propylsilanes functionalized in the 3 position | |
| JP2003137892A (ja) | 3位で官能化されたオルガノシランの製造方法 | |
| EP1756123B1 (en) | Process for making haloorganoalkoxysilanes | |
| JP4584311B2 (ja) | ハロオルガノアルコキシシランの製造方法 | |
| JPH0881473A (ja) | 接触アルキル化方法 | |
| US10968237B2 (en) | Method for continuous production of tetraalkoxysilane | |
| JP3821922B2 (ja) | 四塩化珪素の製造方法 | |
| KR100495988B1 (ko) | 사염화규소의제조방법 | |
| KR950002861B1 (ko) | 트리스실릴메탄들과 그 제조방법 | |
| KR19980059284A (ko) | 비닐클로로실란의 제조방법 | |
| WO2007136541A1 (en) | Process for the production of trialkylsilyl (fluorosulfonyl)difluoroacetate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| MM9K | Patent not in force due to non-payment of renewal fees | ||
| MM9K | Patent not in force due to non-payment of renewal fees |