JP2020520972A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2020520972A5 JP2020520972A5 JP2019564914A JP2019564914A JP2020520972A5 JP 2020520972 A5 JP2020520972 A5 JP 2020520972A5 JP 2019564914 A JP2019564914 A JP 2019564914A JP 2019564914 A JP2019564914 A JP 2019564914A JP 2020520972 A5 JP2020520972 A5 JP 2020520972A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- silane
- formula
- groups
- 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.)
- Granted
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims description 53
- 238000000034 method Methods 0.000 claims description 30
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 25
- 229910000077 silane Inorganic materials 0.000 claims description 25
- 125000003118 aryl group Chemical group 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 239000003960 organic solvent Substances 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 150000004820 halides Chemical class 0.000 claims description 5
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 3
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 3
- 230000003213 activating effect Effects 0.000 claims description 3
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 125000002883 imidazolyl group Chemical group 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 239000011630 iodine Substances 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
- 125000005493 quinolyl group Chemical group 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 150000004756 silanes Chemical class 0.000 claims description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- KZMAWJRXKGLWGS-UHFFFAOYSA-N 2-chloro-n-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-n-(3-methoxypropyl)acetamide Chemical compound S1C(N(C(=O)CCl)CCCOC)=NC(C=2C=CC(OC)=CC=2)=C1 KZMAWJRXKGLWGS-UHFFFAOYSA-N 0.000 claims description 2
- FGUUSXIOTUKUDN-IBGZPJMESA-N C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 Chemical compound C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 FGUUSXIOTUKUDN-IBGZPJMESA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000012190 activator Substances 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 2
- 238000005486 sulfidation Methods 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims description 2
- 125000003396 thiol group Chemical class [H]S* 0.000 claims description 2
- 239000000463 material Substances 0.000 claims 5
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical group ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- -1 pyridadyl group Chemical group 0.000 claims 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical group C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001261 isocyanato group Chemical group *N=C=O 0.000 description 2
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102017211110.0A DE102017211110A1 (de) | 2017-06-30 | 2017-06-30 | Verfahren zur Herstellung eines Silans, Verfahren zur Modifizierung einer Kieselsäure mit dem Silan und modifizierte Kieselsäure |
| DE102017211110.0 | 2017-06-30 | ||
| PCT/EP2018/062293 WO2019001823A1 (de) | 2017-06-30 | 2018-05-14 | Verfahren zur herstellung eines silans, verfahren zur modifizierung einer kieselsäure mit dem silan und modifizierte kieselsäure |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020520972A JP2020520972A (ja) | 2020-07-16 |
| JP2020520972A5 true JP2020520972A5 (enExample) | 2021-02-12 |
| JP6994051B2 JP6994051B2 (ja) | 2022-01-14 |
Family
ID=62165565
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019564914A Active JP6994051B2 (ja) | 2017-06-30 | 2018-05-14 | シランを製造する方法、シランでシリカを変性する方法及び変性シリカ |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US11396601B2 (enExample) |
| EP (1) | EP3645615B1 (enExample) |
| JP (1) | JP6994051B2 (enExample) |
| CN (1) | CN110799582B (enExample) |
| DE (1) | DE102017211110A1 (enExample) |
| ES (1) | ES2895358T3 (enExample) |
| WO (1) | WO2019001823A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102018203652A1 (de) * | 2018-03-12 | 2019-09-12 | Continental Reifen Deutschland Gmbh | Silan, Kautschukmischung enthaltend das Silan und Fahrzeugreifen, der die Kautschukmischung in wenigstens einem Bauteil aufweist |
| DE102019205996A1 (de) * | 2019-04-26 | 2020-10-29 | Continental Reifen Deutschland Gmbh | Silan, Kautschukmischung enthaltend das Silan und Fahrzeugreifen, der die Kautschukmischung in wenigstens einem Bauteil aufweist sowie Verfahren zur Herstellung des Silans |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BG25805A3 (en) | 1972-11-13 | 1978-12-12 | Degussa Ag | A rubber mixture |
| DE2536674C3 (de) | 1975-08-18 | 1979-09-27 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt | Vernetzbare Mischungen auf Basis von Kautschuk, Organosilanen und silikatischen Füllstoffen |
| ES2017015B3 (es) | 1988-04-14 | 1990-12-16 | Soc Nat Elf Aquitaine (Production) | Procedimiento de preparacion de disulfuros y polisulfuros organicos |
| PL193829B1 (pl) | 1996-08-07 | 2007-03-30 | Darwin Discovery Ltd | Pochodne kwasów hydroksamowych, środek farmaceutyczny i zastosowanie pochodnych kwasów hydroksamowych w medycynie |
| JP2002201312A (ja) | 2000-10-30 | 2002-07-19 | Yokohama Rubber Co Ltd:The | ゴム改質剤及びそれを含むゴム組成物 |
| DE102004022399A1 (de) * | 2004-05-06 | 2005-12-01 | Consortium für elektrochemische Industrie GmbH | Partikel enthaltende silanvernetzbare Beschichtungsformulierungen |
| JP2008163125A (ja) * | 2006-12-27 | 2008-07-17 | Bridgestone Corp | ゴム組成物およびそれを用いた空気入りタイヤ |
| US8378094B2 (en) | 2008-01-08 | 2013-02-19 | Johns Manville | Polymerization initiators for fiber-reinforced polymer composites and materials made from the composites |
| EP2110414A1 (de) * | 2008-04-18 | 2009-10-21 | Nanoresins AG | Oberflächenmodifizierte Siliziumdioxid-Partikel |
| WO2010126920A2 (en) * | 2009-04-29 | 2010-11-04 | Henkel Corporation | Moisture curable polydisulfides |
| WO2014074427A1 (en) * | 2012-11-12 | 2014-05-15 | 3M Innovative Properties Company | Addition-fragmentation agents |
| DE102013108937A1 (de) * | 2013-08-19 | 2015-02-19 | Continental Reifen Deutschland Gmbh | Schwefelvernetzbare Kautschukmischung |
| DE102014209226A1 (de) * | 2014-05-15 | 2015-11-19 | Evonik Degussa Gmbh | Harnstoffhaltige Silane, Verfahren zu deren Herstellung und deren Verwendung |
| DE102014209255A1 (de) | 2014-05-15 | 2015-11-19 | Continental Reifen Deutschland Gmbh | Schwefelvernetzbare Kautschukmischung und Fahrzeugreifen |
| DE102014209215A1 (de) | 2014-05-15 | 2015-11-19 | Evonik Degussa Gmbh | Verfahren zur Herstellung von harnstoffhaltigen Silanen |
| DE102017211109A1 (de) * | 2017-06-30 | 2019-01-03 | Continental Reifen Deutschland Gmbh | Silan, Kautschukmischung enthaltend das Silan und Fahrzeugreifen, der die Kautschukmischung in wenigstens einem Bauteil aufweist |
| DE102018203652A1 (de) * | 2018-03-12 | 2019-09-12 | Continental Reifen Deutschland Gmbh | Silan, Kautschukmischung enthaltend das Silan und Fahrzeugreifen, der die Kautschukmischung in wenigstens einem Bauteil aufweist |
| EP3594283B1 (de) * | 2018-07-13 | 2021-04-07 | Continental Reifen Deutschland GmbH | Schwefelvernetzbare kautschukmischung, vulkanisat und fahrzeugreifen |
-
2017
- 2017-06-30 DE DE102017211110.0A patent/DE102017211110A1/de not_active Withdrawn
-
2018
- 2018-05-14 CN CN201880042914.0A patent/CN110799582B/zh active Active
- 2018-05-14 EP EP18724529.5A patent/EP3645615B1/de active Active
- 2018-05-14 US US16/622,970 patent/US11396601B2/en active Active
- 2018-05-14 WO PCT/EP2018/062293 patent/WO2019001823A1/de not_active Ceased
- 2018-05-14 JP JP2019564914A patent/JP6994051B2/ja active Active
- 2018-05-14 ES ES18724529T patent/ES2895358T3/es active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5969387B2 (ja) | ヒドロシリル化触媒 | |
| CN102942585B (zh) | 含琥珀酸酐基的环状有机硅氧烷、其制备方法、有机硅氧烷组合物及热固化性树脂组合物 | |
| JPH11255738A5 (enExample) | ||
| JPS63305133A (ja) | オルガノポリシロキサンの製造方法、および新規オルガノポリシロキサン | |
| JP2020520972A5 (enExample) | ||
| JPS6038399B2 (ja) | β−アミノシラン及びβ−アミノシロキサンの製法 | |
| EP0008902B1 (en) | Process for the preparation of a functionalised solid product | |
| CN105884816B (zh) | 制备含脲硅烷的方法 | |
| JPH0674277B2 (ja) | シリルカルバメ−トおよびその製法 | |
| Pestunovich et al. | N-[hydroxy (dimethyl) silylmethyl]-N, N′-propylene urea hydrochloride: Synthesis and structure | |
| JP2018165261A (ja) | ボロシロキサンの製造方法 | |
| JPH0366641A (ja) | 含フッ素カルボン酸誘導体及びその製造方法 | |
| JP5333971B2 (ja) | β−シアノエステル基を含有する有機ケイ素化合物の製造方法 | |
| JP3181380B2 (ja) | １−アザ−２−シラシクロペンタン化合物の製造方法 | |
| JP5242676B2 (ja) | β−ケトカルボニル官能性有機ケイ素化合物の製造方法 | |
| JP2011246391A (ja) | シリル基で保護されたアミノ基とカルボン酸エステル基を有するシラン化合物及びその製造方法 | |
| JPH064650B2 (ja) | オルガノシロキサンの製造法 | |
| JP5170834B2 (ja) | 脱アルコール型室温硬化性シリコーンゴム組成物の保存安定性付与剤 | |
| US4145359A (en) | Short chain linear amidosiloxanes | |
| JP6354721B2 (ja) | ジフェニルエチル基及びメトキシシリル基を有する有機ケイ素化合物並びにその製造方法 | |
| JPH09100352A (ja) | ポリシロキサン及びその製造方法 | |
| CN110799582A (zh) | 硅烷生产方法、硅烷改性二氧化硅的方法及改性二氧化硅 | |
| US5049688A (en) | Allyl cyclosilalactams | |
| Hasegawa et al. | Cleavage of the SiO–Si (CH3) 2H bond in Si8O20 [Si (CH3) 2H] 8 | |
| JPH06107671A (ja) | 有機ケイ素化合物及びその製造方法 |