JP2005139180A5 - - Google Patents
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- Publication number
- JP2005139180A5 JP2005139180A5 JP2004321201A JP2004321201A JP2005139180A5 JP 2005139180 A5 JP2005139180 A5 JP 2005139180A5 JP 2004321201 A JP2004321201 A JP 2004321201A JP 2004321201 A JP2004321201 A JP 2004321201A JP 2005139180 A5 JP2005139180 A5 JP 2005139180A5
- Authority
- JP
- Japan
- Prior art keywords
- rhodium
- compounds
- hydroformylation
- iridium
- cobalt
- 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.)
- Withdrawn
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- 239000003054 catalyst Substances 0.000 description 8
- 229910052703 rhodium Inorganic materials 0.000 description 8
- 239000010948 rhodium Substances 0.000 description 8
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical class [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 8
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 6
- 238000007037 hydroformylation reaction Methods 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 229910017052 cobalt Inorganic materials 0.000 description 4
- 239000010941 cobalt Substances 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052741 iridium Inorganic materials 0.000 description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 3
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 150000003283 rhodium Chemical class 0.000 description 3
- 150000003284 rhodium compounds Chemical class 0.000 description 3
- -1 alkylbenzene phosphates Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 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 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000002504 iridium compounds Chemical class 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- QHJWOSHIGFDANE-UHFFFAOYSA-N prop-2-enylphosphane Chemical class PCC=C QHJWOSHIGFDANE-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000003304 ruthenium compounds Chemical class 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10352260A DE10352260B3 (de) | 2003-11-08 | 2003-11-08 | Verfahren zur Herstellung von TCD-Alkohol DM |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005139180A JP2005139180A (ja) | 2005-06-02 |
| JP2005139180A5 true JP2005139180A5 (OSRAM) | 2007-10-11 |
Family
ID=34306426
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004321201A Withdrawn JP2005139180A (ja) | 2003-11-08 | 2004-11-04 | Ｔｃｄ−アルコールｄｍの製造方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6939997B2 (OSRAM) |
| EP (1) | EP1529768B1 (OSRAM) |
| JP (1) | JP2005139180A (OSRAM) |
| KR (1) | KR20050044847A (OSRAM) |
| CN (1) | CN100352794C (OSRAM) |
| AT (1) | ATE374739T1 (OSRAM) |
| DE (2) | DE10352260B3 (OSRAM) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004027955B3 (de) * | 2004-06-08 | 2006-01-05 | Celanese Chemicals Europe Gmbh | Verfahren zur Herstellung TCD-Alkohol DM |
| DE102005056393A1 (de) * | 2005-11-24 | 2007-05-31 | Grünenthal GmbH | Multicyclische Verbindungen in druckempfindlichen Klebstoffen |
| DE102007034866A1 (de) | 2007-07-24 | 2009-01-29 | Evonik Degussa Gmbh | Ungesättigte Polyester |
| DE102007034865A1 (de) | 2007-07-24 | 2009-01-29 | Evonik Degussa Gmbh | Beschichtungsstoffzusammensetzungen |
| TWI361181B (en) * | 2007-12-31 | 2012-04-01 | Ind Tech Res Inst | A hydroformylation process |
| US8915736B2 (en) | 2010-09-30 | 2014-12-23 | Voco Gmbh | Composition comprising a monomer with a polyalicyclic structure element for filling and/or sealing a root canal |
| EP2436365B1 (de) | 2010-09-30 | 2017-03-08 | VOCO GmbH | Kompositmaterial umfassend ein Monomer mit einem polyalicyclischen Strukturelement |
| EP2436366B1 (de) | 2010-09-30 | 2015-07-29 | VOCO GmbH | Kompositmaterial umfassend ein Monomer mit einem polyalicyclischen Strukturelement als Versiegelungsmaterial |
| US8697769B2 (en) | 2010-09-30 | 2014-04-15 | Voco Gmbh | Lacquer composition comprising a monomer with a polyalicyclic structure element |
| EP2436668B1 (de) | 2010-09-30 | 2012-09-12 | VOCO GmbH | Polymerisierbare Verbindungen umfassend ein polyalicyclisches Strukturelement |
| EP2450025B1 (de) | 2010-11-08 | 2012-11-28 | VOCO GmbH | Polymerisierbare Phosphorsäurederivate umfassend ein polyalicyclisches Strukturelement |
| EP2578200B1 (de) | 2011-10-04 | 2018-03-28 | VOCO GmbH | Zusammensetzungen zum Infiltrieren und/oder Versiegeln von Zahnhartsubstanz und entsprechende Verfahren |
| DE102012001978A1 (de) | 2012-02-02 | 2013-08-08 | Voco Gmbh | Dentale Kompositmaterialien enthaltend tricyclische Weichmacher |
| DE102012001979A1 (de) | 2012-02-02 | 2013-08-08 | Voco Gmbh | Härtbares Gemisch umfassend Weichmacher mit einem polyalicyclischen Strukturelement zur Anwendung bei der Herstellung dentaler Werkstoffe |
| DE102012016433A1 (de) | 2012-08-17 | 2014-05-15 | Oxea Gmbh | Kontinuierliches Verfahren zur Herstellung primärer aliphatischer Amine aus Aldehyden |
| CN103396293B (zh) * | 2013-08-28 | 2015-02-04 | 中国科学院新疆理化技术研究所 | 一种合成三环癸烷二甲醇的方法 |
| CN103626635A (zh) * | 2013-11-28 | 2014-03-12 | 中国科学院新疆理化技术研究所 | 一种合成三环癸烷二甲醇的方法 |
| CN104387233B (zh) * | 2014-11-29 | 2016-01-06 | 中国科学院新疆理化技术研究所 | 一种合成三环癸烷二甲醇的方法 |
| US10050519B2 (en) | 2016-12-02 | 2018-08-14 | Vlt, Inc. | Control of buck-boost power converter with input voltage tracking |
| DE102018114690A1 (de) | 2018-06-19 | 2019-12-19 | Voco Gmbh | Thermowirksame dentale Kompositzusammensetzung |
| US10538472B1 (en) | 2019-02-14 | 2020-01-21 | Dairen Chemical Corporation | Extraction process for high-boiling aldehyde product separation and catalyst recovery |
| EP4582465A3 (en) * | 2019-02-14 | 2025-09-17 | Dairen Chemical Corporation | Tricyclodecane dimethanol compositions and uses thereof |
| CN112898122A (zh) * | 2019-12-03 | 2021-06-04 | 中国科学院大连化学物理研究所 | 一种由混合辛烯制备异壬醇的方法 |
| US10767004B1 (en) | 2020-01-13 | 2020-09-08 | Dairen Chemical Corporation | Tricyclodecane dimethanol composition and uses thereof |
| DE102020108726A1 (de) * | 2020-03-30 | 2021-09-30 | Carl Zeiss Jena Gmbh | Immersionsöle mit hoher Gebrauchsdauer |
| CN113717029A (zh) * | 2020-05-26 | 2021-11-30 | 中国科学院大连化学物理研究所 | 一种由丁烯齐聚物制备高碳醇的方法 |
| KR102444853B1 (ko) | 2021-06-04 | 2022-09-19 | 에스케이케미칼 주식회사 | 트리사이클로데칸 디메탄올 조성물 및 이의 제조방법 |
| KR102389695B1 (ko) | 2021-06-18 | 2022-04-21 | 에스케이케미칼 주식회사 | 트리사이클로데칸 디메탄올 조성물 및 이의 제조방법 |
| KR102435355B1 (ko) | 2021-06-29 | 2022-08-22 | 에스케이케미칼 주식회사 | 트리사이클로데칸 디메탄올 조성물 및 이의 제조방법 |
| EP4495096A4 (en) * | 2022-03-17 | 2025-10-29 | Mitsubishi Chem Corp | Composition of tricyclodecanedimethanol, UV-curable composition, polymer composition, and process for producing tricyclodecanedimethanol composition |
| JP7726394B2 (ja) * | 2023-04-21 | 2025-08-20 | 三菱ケミカル株式会社 | 環状ジエン含有組成物、アルデヒドの製造方法、アルコールの製造方法、及び環状ジエン含有組成物の製造方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2928313A1 (de) | 1979-07-13 | 1981-02-05 | Ruhrchemie Ag | Verfahren zur herstellung von 3-(4)- formyltricyclo- eckige klammer auf 5,2,1, 0 hoch 2,6 eckige klammer zu -decen-8 |
| JPS5630938A (en) * | 1979-08-23 | 1981-03-28 | Mitsubishi Petrochem Co Ltd | Preparation of tricyclodecanedialdehyde |
| US4229376A (en) | 1979-09-10 | 1980-10-21 | Henkel Corporation | Polycyclic polyamines |
| US4319049A (en) * | 1980-10-06 | 1982-03-09 | Henkel Corporation | Bis hydroxymethyl tricyclo (5,2,1,02,6) decane |
| DE3447030A1 (de) * | 1984-12-22 | 1986-07-03 | Ruhrchemie Ag, 4200 Oberhausen | Verfahren zur herstellung von 8- und 9-formyl-tricyclo (5,2,1,0(pfeil hoch)2(pfeil hoch)(pfeil hoch),(pfeil hoch)(pfeil hoch)6(pfeil hoch))-decen-8 |
| DE3822038A1 (de) | 1988-06-30 | 1990-03-01 | Hoechst Ag | Verfahren zur herstellung von 3(4),8(9)-bis-(aminomethyl)-tricyclo (5.2.1.0(pfeil hoch)2(pfeil hoch)(pfeil hoch),(pfeil hoch)(pfeil hoch)6(pfeil hoch))-decan |
| DE19619527A1 (de) | 1996-05-15 | 1997-11-20 | Hoechst Ag | Katalysatorsysteme auf der Basis von Rhodium-Komplexverbindungen mit Diphosphin-Liganden und ihre Verwendung bei der Herstellung von Aldehyden |
| JP3784514B2 (ja) * | 1997-09-29 | 2006-06-14 | 株式会社クラレ | トリシクロデカンジメタノールの製造法 |
| DE60002526T3 (de) * | 1999-07-02 | 2007-08-09 | Mitsubishi Gas Chemical Co., Inc. | Herstellung von Tricyclodecandicarbaldehyd, Pentacyclopentadecandicarbaldehyd und der entsprechenden Dimethanole |
-
2003
- 2003-11-08 DE DE10352260A patent/DE10352260B3/de not_active Expired - Fee Related
-
2004
- 2004-10-18 US US10/967,580 patent/US6939997B2/en not_active Expired - Fee Related
- 2004-10-27 EP EP04025481A patent/EP1529768B1/de not_active Expired - Lifetime
- 2004-10-27 DE DE502004005119T patent/DE502004005119D1/de not_active Expired - Fee Related
- 2004-10-27 AT AT04025481T patent/ATE374739T1/de not_active IP Right Cessation
- 2004-11-04 JP JP2004321201A patent/JP2005139180A/ja not_active Withdrawn
- 2004-11-04 CN CNB200410087194XA patent/CN100352794C/zh not_active Expired - Fee Related
- 2004-11-05 KR KR1020040089954A patent/KR20050044847A/ko not_active Withdrawn
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