CH639392A5 - Phenoxyalkyl-, thio-phenoxyalkyl- und pyridyloxyalkyl-trialkoxy-silane und verfahren zu ihrer herstellung. - Google Patents

Phenoxyalkyl-, thio-phenoxyalkyl- und pyridyloxyalkyl-trialkoxy-silane und verfahren zu ihrer herstellung. Download PDF

Info

Publication number: CH639392A5
Authority: CH; Switzerland
Prior art keywords: phenoxyalkyl; silane; alkyl; carbon atoms; compounds
Prior art date: 1978-04-26

Application number

CH378979A

Other languages

German (de)

English (en)

Inventor

Abe Berger

Irwin Bruce Silverstein

Original Assignee

M & T Chemicals Inc

Priority date (The priority date 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 date listed.)

1978-04-26

Filing date

1979-04-23

Publication date

1983-11-15

1979-04-23 Application filed by M & T Chemicals Inc filed Critical M & T Chemicals Inc

1983-11-15 Publication of CH639392A5 publication Critical patent/CH639392A5/de

Links

238000000034 method Methods 0.000 title claims description 17
150000001875 compounds Chemical class 0.000 claims description 23
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 18
238000006243 chemical reaction Methods 0.000 claims description 14
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 13
229910000077 silane Inorganic materials 0.000 claims description 13
125000004432 carbon atom Chemical group C* 0.000 claims description 12
239000007788 liquid Substances 0.000 claims description 11
238000009835 boiling Methods 0.000 claims description 10
125000001424 substituent group Chemical group 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
239000012429 reaction media Substances 0.000 claims description 9
125000005359 phenoxyalkyl group Chemical group 0.000 claims description 8
239000003513 alkali Substances 0.000 claims description 7
238000002360 preparation method Methods 0.000 claims description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 6
239000000460 chlorine Substances 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 5
239000002904 solvent Substances 0.000 claims description 5
239000004215 Carbon black (E152) Substances 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
150000002430 hydrocarbons Chemical class 0.000 claims description 4
239000007791 liquid phase Substances 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 3
125000003710 aryl alkyl group Chemical group 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
239000012298 atmosphere Substances 0.000 claims description 2
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
101100295738 Gallus gallus COR3 gene Proteins 0.000 claims 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
239000000010 aprotic solvent Substances 0.000 claims 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
229910052708 sodium Inorganic materials 0.000 claims 1
239000011734 sodium Substances 0.000 claims 1
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
239000011541 reaction mixture Substances 0.000 description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
OXYZDRAJMHGSMW-UHFFFAOYSA-N 3-chloropropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCl OXYZDRAJMHGSMW-UHFFFAOYSA-N 0.000 description 5
238000010533 azeotropic distillation Methods 0.000 description 5
239000012808 vapor phase Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
229910052710 silicon Inorganic materials 0.000 description 4
RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
238000002329 infrared spectrum Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
239000000243 solution Substances 0.000 description 3
RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
GRFNBEZIAWKNCO-UHFFFAOYSA-N 3-pyridinol Chemical compound OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 description 2
BKCYLOLTKVUVPA-UHFFFAOYSA-N 4-(3-trimethoxysilylpropoxy)benzaldehyde Chemical compound CO[Si](OC)(OC)CCCOC1=CC=C(C=O)C=C1 BKCYLOLTKVUVPA-UHFFFAOYSA-N 0.000 description 2
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
150000001447 alkali salts Chemical class 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
239000003365 glass fiber Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
239000000203 mixture Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000012299 nitrogen atmosphere Substances 0.000 description 2
-1 phenoxy, thiophenoxy Chemical group 0.000 description 2
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
150000004756 silanes Chemical class 0.000 description 2
239000010703 silicon Substances 0.000 description 2
JDESAODINAIGSD-UHFFFAOYSA-N trimethoxy(3-pyridin-3-yloxypropyl)silane Chemical compound CO[Si](OC)(OC)CCCOC1=CC=CN=C1 JDESAODINAIGSD-UHFFFAOYSA-N 0.000 description 2
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical class NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 description 1
HUPGCAGBHBJUJC-UHFFFAOYSA-N 3-(3-trimethoxysilylpropoxy)aniline Chemical compound CO[Si](OC)(OC)CCCOC1=CC=CC(N)=C1 HUPGCAGBHBJUJC-UHFFFAOYSA-N 0.000 description 1
WAVOOWVINKGEHS-UHFFFAOYSA-N 3-(diethylamino)phenol Chemical compound CCN(CC)C1=CC=CC(O)=C1 WAVOOWVINKGEHS-UHFFFAOYSA-N 0.000 description 1
229940018563 3-aminophenol Drugs 0.000 description 1
FGYPEIBVFQOQKC-UHFFFAOYSA-N 4-(3-trimethoxysilylpropoxy)aniline Chemical compound CO[Si](OC)(OC)CCCOC1=CC=C(N)C=C1 FGYPEIBVFQOQKC-UHFFFAOYSA-N 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
239000011260 aqueous acid Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000002131 composite material Substances 0.000 description 1
229940125810 compound 20 Drugs 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
239000003599 detergent Substances 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000008394 flocculating agent Substances 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
238000005194 fractionation Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical class OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
238000000465 moulding Methods 0.000 description 1
DDESMIQDZAUXOY-UHFFFAOYSA-N n,n-diethyl-3-(3-trimethoxysilylpropoxy)aniline Chemical compound CCN(CC)C1=CC=CC(OCCC[Si](OC)(OC)OC)=C1 DDESMIQDZAUXOY-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000000746 purification Methods 0.000 description 1
UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
125000005554 pyridyloxy group Chemical group 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000000565 sealant Substances 0.000 description 1
238000004513 sizing Methods 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
239000001993 wax Substances 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
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- 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
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/302—Water
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/703—Isocyanates or isothiocyanates transformed in a latent form by physical means
- C08G18/705—Dispersions of isocyanates or isothiocyanates in a liquid medium
- C08G18/706—Dispersions of isocyanates or isothiocyanates in a liquid medium the liquid medium being water
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2125/00—Compositions for processes using internal mould release agents
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/06—Polymer mixtures characterised by other features having improved processability or containing aids for moulding methods
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dispersion Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Materials Engineering (AREA)
Separation Of Suspended Particles By Flocculating Agents (AREA)
Surface Treatment Of Glass Fibres Or Filaments (AREA)
Crystals, And After-Treatments Of Crystals (AREA)

CH378979A 1978-04-26 1979-04-23 Phenoxyalkyl-, thio-phenoxyalkyl- und pyridyloxyalkyl-trialkoxy-silane und verfahren zu ihrer herstellung. CH639392A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US90019778A	1978-04-26	1978-04-26

Publications (1)

Publication Number	Publication Date
CH639392A5 true CH639392A5 (de)	1983-11-15

Family

ID=25412119

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH378979A CH639392A5 (de)	1978-04-26	1979-04-23	Phenoxyalkyl-, thio-phenoxyalkyl- und pyridyloxyalkyl-trialkoxy-silane und verfahren zu ihrer herstellung.

Country Status (15)

Country	Link
JP (1)	JPS54144344A (fr)
KR (1)	KR850000074B1 (fr)
BE (1)	BE875801A (fr)
CA (1)	CA1109889A (fr)
CH (1)	CH639392A5 (fr)
DE (1)	DE2915072A1 (fr)
DK (1)	DK148710C (fr)
ES (1)	ES479900A1 (fr)
FR (1)	FR2424281B1 (fr)
GB (1)	GB2019862B (fr)
IT (1)	IT1165955B (fr)
MX (1)	MX149694A (fr)
NL (1)	NL7903128A (fr)
NO (2)	NO156610C (fr)
SE (1)	SE7903595L (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES491385A0 (es) *	1979-08-08	1981-05-16		Un metodo para preparar un silano
CA1152512A (fr) *	1979-08-31	1983-08-23	Abe Berger	Preparation d'aryloxyalkylsilanes
JP2630596B2 (ja) *	1987-07-27	1997-07-16	株式会社ブリヂストン	シランカップリング剤
DE3935638A1 (de) *	1989-10-26	1991-05-02	Consortium Elektrochem Ind	Organosilylalkylaromaten
JP5245076B2 (ja) *	2008-09-30	2013-07-24	大同化学工業株式会社	廃液の処理方法
JP5360814B2 (ja) *	2009-03-12	2013-12-04	独立行政法人産業技術総合研究所	有機無機複合材料の製造方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1054041A (fr) *		1900-01-01
GB1062418A (en) *	1964-01-27	1967-03-22	Ici Ltd	New nitrogen-containing siloxanes
US3355425A (en) *	1964-08-06	1967-11-28	Dow Corning	Organopolysiloxanes
DE2215629A1 (de) *	1972-03-30	1973-10-04	Dynamit Nobel Ag	Kernsubstituierte aralkylsilane
FR2226407B1 (fr) *	1973-04-17	1978-05-26	Rhone Progil
US3926911A (en) *	1973-06-07	1975-12-16	Ciba Geigy Corp	Crosslinked polymers containing siloxane groups
FR2245663A1 (en) *	1973-08-17	1975-04-25	Rhone Progil	Aminophenoxy alkyl silanes and dimers, polymers - by catalytic hydrogenation of corresponding nitrophenols
FR2243022B1 (fr) *	1973-09-10	1977-09-23	Rhone Progil

1979
- 1979-04-03 GB GB7911609A patent/GB2019862B/en not_active Expired
- 1979-04-06 KR KR7901084A patent/KR850000074B1/ko active
- 1979-04-12 DE DE19792915072 patent/DE2915072A1/de active Granted
- 1979-04-13 JP JP4430979A patent/JPS54144344A/ja active Pending
- 1979-04-19 FR FR7909922A patent/FR2424281B1/fr not_active Expired
- 1979-04-20 NL NL7903128A patent/NL7903128A/xx not_active Application Discontinuation
- 1979-04-23 NO NO791349A patent/NO156610C/no unknown
- 1979-04-23 CH CH378979A patent/CH639392A5/de not_active IP Right Cessation
- 1979-04-23 BE BE0/194795A patent/BE875801A/fr not_active IP Right Cessation
- 1979-04-24 IT IT09404/79A patent/IT1165955B/it active
- 1979-04-24 SE SE7903595A patent/SE7903595L/xx not_active Application Discontinuation
- 1979-04-24 MX MX177424A patent/MX149694A/es unknown
- 1979-04-25 CA CA326,358A patent/CA1109889A/fr not_active Expired
- 1979-04-25 DK DK170779A patent/DK148710C/da active IP Right Grant
- 1979-04-25 ES ES479900A patent/ES479900A1/es not_active Expired
1985
- 1985-04-30 NO NO851716A patent/NO851716L/no unknown

Also Published As

Publication number	Publication date
ES479900A1 (es)	1979-11-16
JPS54144344A (en)	1979-11-10
CA1109889A (fr)	1981-09-29
DK148710C (da)	1986-01-27
GB2019862B (en)	1982-05-19
SE7903595L (sv)	1979-10-27
KR830001963A (ko)	1983-05-21
GB2019862A (en)	1979-11-07
DK170779A (da)	1979-10-27
KR850000074B1 (ko)	1985-02-18
DE2915072C2 (fr)	1989-08-10
NO791349L (no)	1979-10-29
FR2424281B1 (fr)	1985-06-28
FR2424281A1 (fr)	1979-11-23
DK148710B (da)	1985-09-09
NL7903128A (nl)	1979-10-30
DE2915072A1 (de)	1979-11-08
MX149694A (es)	1983-12-13
NO156610C (no)	1987-10-21
IT7909404A0 (it)	1979-04-24
IT1165955B (it)	1987-04-29
BE875801A (fr)	1979-08-16
NO156610B (no)	1987-07-13
NO851716L (no)	1979-10-29

Legal Events

Date	Code	Title	Description
1990-12-28	PL	Patent ceased

Publication	Publication Date	Title
DE69521001T2 (de)	2001-09-06	Verfahren zur Herstellung von Silanpolysulfiden
EP0638575B1 (fr)	1999-01-27	Procédé de préparation de diorganodialcoxysilanes
EP0437653A1 (fr)	1991-07-24	Procédé de prÀ©paration d'organosilanes contenant des groupes méthacryloxy ou acryloxy
DE2642811C3 (de)	1980-02-14	Oxysilanol-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung
DE2365272C2 (fr)	1988-02-18
DE2642835B2 (de)	1979-10-11	Oxysilan-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung
CH451933A (de)	1968-05-15	Verfahren zur Herstellung von siliciumorganischen Verbindungen
EP0348620B1 (fr)	1994-08-31	Procédé pour la préparation de thiourées organyloxysilyl fonctionnelles mono- ou polysubstituées et ces composés
DE2325878A1 (de)	1974-12-12	Phenoxyderivate des trifluormethylbenzols und verfahren zu deren herstellung
CH639392A5 (de)	1983-11-15	Phenoxyalkyl-, thio-phenoxyalkyl- und pyridyloxyalkyl-trialkoxy-silane und verfahren zu ihrer herstellung.
DE69029066T2 (de)	1997-05-28	Abkömmlinge von fluorierten Carbonsäuren und Verfahren zu deren Herstellung
EP0387689B1 (fr)	1994-06-22	Procédé de préparation de composés organiques du silicium
DE3025034A1 (de)	1981-02-26	Silane und verfahren zu ihrer herstellung
DE2832346C3 (de)	1982-03-25	Verfahren zur Herstellung von Hydroxyalkyl-perfluoralkan-sulfonamiden
DE69010098T2 (de)	1994-11-17	Verfahren zur Herstellung von silylfunktionalen Fumaraten.
DE3703484C1 (fr)	1988-09-15
DE69813380T2 (de)	2003-12-04	Verfahren zur Herstellung von 16-Dehydro Vitamin D Verbindungen
DE69402832T2 (de)	1997-07-31	Verfahren zur herstellung von bis(2-benzoxazolyl)stilbenen
CH544058A (de)	1973-12-28	Verfahren zur Herstellung von Polyfluoralkylestern von Fumarsäure und verwandten Säuren
DE4034613A1 (de)	1992-05-07	Alkoxysilylgruppen aufweisende pyridiniumsalze
DE3415475A1 (de)	1985-11-07	Verfahren zur herstellung von alkoxymethylenverbindungen von essigestern und substituierten essigestern
DE3632464C2 (fr)	1990-11-29
EP0031436A2 (fr)	1981-07-08	Procédé de dissociation de siloxanes
DE2100556B2 (de)	1974-03-07	Verfahren zur Herstellung von Aminoaryltrialkoxy- und -triphenoxysilanverbindungen
EP0003299A1 (fr)	1979-08-08	Esters silyliques des acides perfluoroalcanesulfoniques ainsi qu'un procédé pour leur préparation