BE553602A - - Google Patents
Info
- Publication number
- BE553602A BE553602A BE553602DA BE553602A BE 553602 A BE553602 A BE 553602A BE 553602D A BE553602D A BE 553602DA BE 553602 A BE553602 A BE 553602A
- Authority
- BE
- Belgium
- Prior art keywords
- alpha
- reaction
- process according
- sep
- cyanoalkylsilane
- Prior art date
Links
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 19
- 238000006460 hydrolysis reaction Methods 0.000 claims description 15
- 229910000077 silane Inorganic materials 0.000 claims description 15
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 14
- 230000007062 hydrolysis Effects 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- 150000002825 nitriles Chemical class 0.000 claims description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 7
- 239000011541 reaction mixture Substances 0.000 claims description 7
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical group C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
- 238000009835 boiling Methods 0.000 description 21
- -1 alpha-cyanoethyldiethylchlorosilane Chemical compound 0.000 description 19
- JHVCHXGNRUSRFD-UHFFFAOYSA-N 2-trichlorosilylpropanenitrile Chemical compound N#CC(C)[Si](Cl)(Cl)Cl JHVCHXGNRUSRFD-UHFFFAOYSA-N 0.000 description 12
- 150000004756 silanes Chemical class 0.000 description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 229910052710 silicon Inorganic materials 0.000 description 10
- 238000005194 fractionation Methods 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 8
- 229910052753 mercury Inorganic materials 0.000 description 8
- 239000007858 starting material Substances 0.000 description 8
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 7
- 239000005052 trichlorosilane Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 238000010183 spectrum analysis Methods 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 229910052697 platinum Inorganic materials 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- YGRRKBIBZARMJZ-UHFFFAOYSA-N 2-[dichloro(phenyl)silyl]propanenitrile Chemical compound N#CC(C)[Si](Cl)(Cl)C1=CC=CC=C1 YGRRKBIBZARMJZ-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- JVIIJIYEVTWYJY-UHFFFAOYSA-N 2-[dichloro(methyl)silyl]propanenitrile Chemical compound N#CC(C)[Si](C)(Cl)Cl JVIIJIYEVTWYJY-UHFFFAOYSA-N 0.000 description 2
- ABPCWITVPBTZDI-UHFFFAOYSA-N 2-silylpropanenitrile Chemical class [SiH3]C(C#N)C ABPCWITVPBTZDI-UHFFFAOYSA-N 0.000 description 2
- DXYXZPDAEJYSJL-UHFFFAOYSA-N 2-triethoxysilylpropanenitrile Chemical compound CCO[Si](OCC)(OCC)C(C)C#N DXYXZPDAEJYSJL-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 230000002939 deleterious effect Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- SKJVXNIMISTFMU-UHFFFAOYSA-N 2-ethenoxypropanenitrile Chemical group N#CC(C)OC=C SKJVXNIMISTFMU-UHFFFAOYSA-N 0.000 description 1
- KNCSAXYBNAEWKN-UHFFFAOYSA-N 2-methyl-2-trichlorosilylpropanenitrile Chemical compound N#CC(C)(C)[Si](Cl)(Cl)Cl KNCSAXYBNAEWKN-UHFFFAOYSA-N 0.000 description 1
- QGMUHAUTIHAMJS-UHFFFAOYSA-N 2-trichlorosilylbutanenitrile Chemical compound CCC(C#N)[Si](Cl)(Cl)Cl QGMUHAUTIHAMJS-UHFFFAOYSA-N 0.000 description 1
- OLBGECWYBGXCNV-UHFFFAOYSA-N 3-trichlorosilylpropanenitrile Chemical compound Cl[Si](Cl)(Cl)CCC#N OLBGECWYBGXCNV-UHFFFAOYSA-N 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- NKKMVIVFRUYPLQ-NSCUHMNNSA-N crotononitrile Chemical compound C\C=C\C#N NKKMVIVFRUYPLQ-NSCUHMNNSA-N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- PFMKUUJQLUQKHT-UHFFFAOYSA-N dichloro(ethyl)silicon Chemical compound CC[Si](Cl)Cl PFMKUUJQLUQKHT-UHFFFAOYSA-N 0.000 description 1
- KTQYJQFGNYHXMB-UHFFFAOYSA-N dichloro(methyl)silicon Chemical compound C[Si](Cl)Cl KTQYJQFGNYHXMB-UHFFFAOYSA-N 0.000 description 1
- XNAFLNBULDHNJS-UHFFFAOYSA-N dichloro(phenyl)silicon Chemical compound Cl[Si](Cl)C1=CC=CC=C1 XNAFLNBULDHNJS-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000005048 methyldichlorosilane Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE553602A true BE553602A (enrdf_load_html_response) |
Family
ID=178343
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE553602D BE553602A (enrdf_load_html_response) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE553602A (enrdf_load_html_response) |
-
0
- BE BE553602D patent/BE553602A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1103895A (fr) | Procede de preparation d'hydrogenosilanes | |
| BE560351A (enrdf_load_html_response) | ||
| FR2617854A1 (fr) | Composition a base d'un nouveau polycarbosilane, sa preparation et son application a la fabrication de produits et articles ceramiques a base de carbure de silicium | |
| SE445920B (sv) | Sett att framstella monomera organosilikonestrar | |
| BE553602A (enrdf_load_html_response) | ||
| FR2676063A1 (fr) | Catalyseur halogenure de la phosphonitrile, procede pour sa preparation, composition le contenant et son utilisation pour la polymerisation d'organosiloxanes. | |
| FR2599369A1 (fr) | Procede de preparation de disilylmethanes | |
| BE498176A (enrdf_load_html_response) | ||
| CN113260622B (zh) | 制备官能化有机硅烷醇化合物的方法 | |
| EP0171307B1 (fr) | Procédé de fabrication de composés silylmétallocènes et composés obtenus par ce procédé | |
| EP0325881B1 (fr) | Diorganopolysiloxane à fonction benzylidène-3 camphre | |
| JPH03119029A (ja) | Ｓｉ‐結合共役ジエニル基を有するオルガノ（ポリ）シロキサンの製法 | |
| CA1132995A (fr) | Procede de preparation de polyethers glycidiques de polyphenols | |
| EP0287478B1 (fr) | Procédé de préparation de diamines aromatiques à groupement polydiorganosiloxane | |
| WO2001072672A1 (fr) | Compositions de mono- et polybenzyl-1,2,3,4-tetrahydronaphtalenes, utilisation desdites compositions ou d'un melange d'isomeres du monobenzyl-1,2,3,4-tetrahydronaphtalene comme fluide de transfert de chaleur | |
| FR2514360A1 (fr) | Preparation de polydimethylsiloxanes lineaires | |
| SU435243A1 (enrdf_load_html_response) | ||
| BE553606A (enrdf_load_html_response) | ||
| FR2831544A1 (fr) | Procede de preparation d'huiles silicones portant un groupement contenant au moins un cycle hydrocarbone dans lequel est inclus un atome d'oxygene | |
| BE476174A (enrdf_load_html_response) | ||
| FR2545827A1 (fr) | Procede de preparation d'organosiloxanes et d'halogenures d'alkyle a partir de dialkyldialcoxysilanes | |
| BE565569A (enrdf_load_html_response) | ||
| BE496045A (enrdf_load_html_response) | ||
| BE484771A (enrdf_load_html_response) | ||
| BE491765R (enrdf_load_html_response) |