JP2007512400A5 - - Google Patents
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- Publication number
- JP2007512400A5 JP2007512400A5 JP2006540334A JP2006540334A JP2007512400A5 JP 2007512400 A5 JP2007512400 A5 JP 2007512400A5 JP 2006540334 A JP2006540334 A JP 2006540334A JP 2006540334 A JP2006540334 A JP 2006540334A JP 2007512400 A5 JP2007512400 A5 JP 2007512400A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbonyl
- polyorganosiloxane
- alkyl
- sio
- 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.)
- Pending
Links
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 13
- -1 sulfono radical Chemical class 0.000 claims description 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
- 150000002148 esters Chemical class 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- 125000003277 amino group Chemical group 0.000 claims description 9
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims description 8
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 6
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- CYFLXLSBHQBMFT-UHFFFAOYSA-N sulfamoxole Chemical group O1C(C)=C(C)N=C1NS(=O)(=O)C1=CC=C(N)C=C1 CYFLXLSBHQBMFT-UHFFFAOYSA-N 0.000 claims description 5
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 5
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 4
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 2
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 22
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 7
- 239000007800 oxidant agent Substances 0.000 claims 7
- 125000004122 cyclic group Chemical group 0.000 claims 5
- 229910004283 SiO 4 Inorganic materials 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 229910052796 boron Inorganic materials 0.000 claims 3
- 125000000962 organic group Chemical group 0.000 claims 3
- 230000001590 oxidative effect Effects 0.000 claims 3
- 229910052698 phosphorus Inorganic materials 0.000 claims 3
- 229910052710 silicon Inorganic materials 0.000 claims 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 239000012071 phase Substances 0.000 claims 2
- XUXUHDYTLNCYQQ-UHFFFAOYSA-N 4-amino-TEMPO Chemical group CC1(C)CC(N)CC(C)(C)N1[O] XUXUHDYTLNCYQQ-UHFFFAOYSA-N 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- QYTDEUPAUMOIOP-UHFFFAOYSA-N TEMPO Chemical group CC1(C)CCCC(C)(C)N1[O] QYTDEUPAUMOIOP-UHFFFAOYSA-N 0.000 claims 1
- 239000003570 air Substances 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- YLFIGGHWWPSIEG-UHFFFAOYSA-N aminoxyl Chemical compound [O]N YLFIGGHWWPSIEG-UHFFFAOYSA-N 0.000 claims 1
- 239000008346 aqueous phase Substances 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 239000007844 bleaching agent Substances 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 claims 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000004966 inorganic peroxy acids Chemical class 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 claims 1
- YUUWVCDKDHHAFI-UHFFFAOYSA-N n-sulfanylhydroxylamine Chemical compound ONS YUUWVCDKDHHAFI-UHFFFAOYSA-N 0.000 claims 1
- 150000001451 organic peroxides Chemical class 0.000 claims 1
- 150000004967 organic peroxy acids Chemical class 0.000 claims 1
- 239000012074 organic phase Substances 0.000 claims 1
- 125000000466 oxiranyl group Chemical group 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000012048 reactive intermediate Substances 0.000 claims 1
- 238000004381 surface treatment Methods 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 150000003927 aminopyridines Chemical class 0.000 description 1
- 150000005010 aminoquinolines Chemical class 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000004806 hydroxypyridines Chemical class 0.000 description 1
- VDBNYAPERZTOOF-UHFFFAOYSA-N isoquinolin-1(2H)-one Chemical class C1=CC=C2C(=O)NC=CC2=C1 VDBNYAPERZTOOF-UHFFFAOYSA-N 0.000 description 1
- 150000002537 isoquinolines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical class C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2003154259 DE10354259A1 (de) | 2003-11-20 | 2003-11-20 | Verfahren zur Herstellung von Carbonylreste-aufweisenden Organosiliciumverbindungen |
| PCT/EP2004/013137 WO2005049697A2 (de) | 2003-11-20 | 2004-11-18 | Verfahren zur herstellung von carbonylreste-aufweisenden organosiliciumverbindungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007512400A JP2007512400A (ja) | 2007-05-17 |
| JP2007512400A5 true JP2007512400A5 (https=) | 2009-02-05 |
Family
ID=34559707
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006540334A Pending JP2007512400A (ja) | 2003-11-20 | 2004-11-18 | カルボニル基を有する有機ケイ素化合物の製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7700196B2 (https=) |
| EP (1) | EP1685183B1 (https=) |
| JP (1) | JP2007512400A (https=) |
| CN (1) | CN100528937C (https=) |
| DE (2) | DE10354259A1 (https=) |
| WO (1) | WO2005049697A2 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007011465A1 (en) | 2005-07-18 | 2007-01-25 | Dow Corning Corporation | Aldehyde functional siloxanes |
| US7696294B2 (en) | 2006-08-02 | 2010-04-13 | Honeywell International Inc. | Siloxane polymers and uses thereof |
| WO2008016957A2 (en) * | 2006-08-02 | 2008-02-07 | Honeywell International Inc. | Siloxane polymers and uses thereof |
| DE102007047211A1 (de) * | 2007-10-02 | 2009-04-09 | Wacker Chemie Ag | Entschäumerzusammensetzungen |
| JP5413710B2 (ja) * | 2008-06-11 | 2014-02-12 | 日本電気株式会社 | 電極活物質と、その製造方法及びそれを用いた電池 |
| KR101057191B1 (ko) * | 2008-12-30 | 2011-08-16 | 주식회사 하이닉스반도체 | 반도체 소자의 미세 패턴 형성방법 |
| EP2617703B1 (en) | 2012-01-17 | 2014-07-30 | Corning Incorporated | Improved catalyzed hypohalous oxidation of alcohol groups |
| US20150209808A1 (en) * | 2014-01-24 | 2015-07-30 | The Procter & Gamble Company | Package for Light Activated Treatment Composition |
| JP2017536468A (ja) | 2014-09-23 | 2017-12-07 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | アミノ酸系基質の処理のためのシリコーン化合物およびその組成物 |
| US11179312B2 (en) | 2017-06-05 | 2021-11-23 | Momentive Performance Materials Inc. | Aqueous compositions for the treatment of hair |
| EP3581697B1 (en) | 2018-06-11 | 2023-02-22 | The Procter & Gamble Company | Photoactivating device for washing machine |
| US11090255B2 (en) | 2018-12-04 | 2021-08-17 | Momentive Performance Materials Inc. | Use of polycarboxylic acid compounds for the treatment of fibrious amino acid based substrates, especially hair |
| CN119053641A (zh) * | 2022-04-21 | 2024-11-29 | 信越化学工业株式会社 | 醛改性有机硅及其制造方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2803637A (en) * | 1954-01-18 | 1957-08-20 | Dow Corning | Organosiloxane aldehydes |
| US2947770A (en) * | 1955-05-13 | 1960-08-02 | Union Carbide Corp | Diformylbutyl and diformylcyclopentyl containing siloxanes |
| US2970150A (en) | 1957-12-17 | 1961-01-31 | Union Carbide Corp | Processes for the reaction of silanic hydrogen-bonded siloxanes with unsaturated organic compounds with a platinum catalyst |
| DE3632869A1 (de) | 1986-09-26 | 1988-03-31 | Bayer Ag | Polysiloxane |
| FR2636067B1 (fr) * | 1988-09-05 | 1990-05-18 | Rhone Poulenc Chimie | Polyorganosiloxane a fonction propanaldehyde et son procede de preparation par hydroformylation |
| FR2645867B1 (fr) | 1989-04-13 | 1991-06-14 | Rhone Poulenc Chimie | Procede de preparation, par hydroformylation, de polyorganosiloxane a fonction propanaldehyde |
| FR2647801B1 (fr) | 1989-06-02 | 1991-09-13 | Rhone Poulenc Chimie | Composition durcissable, sous un rayonnement, a base de polyorganosiloxane a fonction propanaldehyde |
| DE4306041A1 (de) | 1993-02-26 | 1994-09-01 | Wacker Chemie Gmbh | Glycosidreste aufweisende Organosiliciumverbindungen und Verfahren zu deren Herstellung |
| US5739246A (en) * | 1997-03-06 | 1998-04-14 | Dow Corning Corporation | Preparation of carbonyl functional polysiloxanes |
| BR9910274A (pt) * | 1998-05-07 | 2001-01-02 | Tno | Processo para a oxidação de um álcool primário |
| US6121404A (en) * | 1998-07-06 | 2000-09-19 | Dow Corning Corporation | β-diketo functional organosilicon compounds |
| JP4394230B2 (ja) * | 1999-12-13 | 2010-01-06 | 高砂香料工業株式会社 | ３−メチル−２，４−ノナンジオンの製造法 |
| DE10029597A1 (de) * | 2000-06-15 | 2002-01-03 | Degussa | Verfahren zur Oxidation von Alkoholen mit homogen löslichen polymervergrößerten Stickstoffverbindungen als Katalysator |
| JP2003073332A (ja) * | 2001-06-20 | 2003-03-12 | Kuraray Co Ltd | ２−オキソカルボン酸エステル類の製造方法 |
| ATE257136T1 (de) | 2001-10-11 | 2004-01-15 | Consortium Elektrochem Ind | Verfahren zur oxidation von alkoholen unter katalyse von nitroxylverbindungen |
-
2003
- 2003-11-20 DE DE2003154259 patent/DE10354259A1/de not_active Withdrawn
-
2004
- 2004-11-18 EP EP04797999A patent/EP1685183B1/de not_active Expired - Lifetime
- 2004-11-18 CN CNB2004800407116A patent/CN100528937C/zh not_active Expired - Fee Related
- 2004-11-18 DE DE200450005985 patent/DE502004005985D1/de not_active Expired - Lifetime
- 2004-11-18 JP JP2006540334A patent/JP2007512400A/ja active Pending
- 2004-11-18 US US10/595,955 patent/US7700196B2/en not_active Expired - Fee Related
- 2004-11-18 WO PCT/EP2004/013137 patent/WO2005049697A2/de not_active Ceased
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