JP2005535455A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005535455A5 JP2005535455A5 JP2005506118A JP2005506118A JP2005535455A5 JP 2005535455 A5 JP2005535455 A5 JP 2005535455A5 JP 2005506118 A JP2005506118 A JP 2005506118A JP 2005506118 A JP2005506118 A JP 2005506118A JP 2005535455 A5 JP2005535455 A5 JP 2005535455A5
- Authority
- JP
- Japan
- Prior art keywords
- mmol
- added
- cannula
- orange
- reaction
- 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
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- 239000003039 volatile agent Substances 0.000 description 6
- 238000001914 filtration Methods 0.000 description 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- VEFLKXRACNJHOV-UHFFFAOYSA-N 1,3-dibromopropane Chemical compound BrCCCBr VEFLKXRACNJHOV-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical compound C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- -1 di-1-adamantylphosphinomethyl Chemical group 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 1
- PGGKLIWTIWFQMO-UHFFFAOYSA-N CC1=CC=C([Na])C([Na])=C1C Chemical compound CC1=CC=C([Na])C([Na])=C1C PGGKLIWTIWFQMO-UHFFFAOYSA-N 0.000 description 1
- 244000248349 Citrus limon Species 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 229910010082 LiAlH Inorganic materials 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- MIZJPSACHCOTRL-UHFFFAOYSA-N bis(1-adamantyl)-[[2-[bis(1-adamantyl)phosphanylmethyl]phenyl]methyl]phosphane Chemical compound C1C(C2)CC(C3)CC2CC13P(C12CC3CC(CC(C3)C1)C2)CC1=CC=CC=C1CP(C12CC3CC(CC(C3)C1)C2)C1(C2)CC(C3)CC2CC3C1 MIZJPSACHCOTRL-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- SYXYWTXQFUUWLP-UHFFFAOYSA-N sodium;butan-1-olate Chemical compound [Na+].CCCC[O-] SYXYWTXQFUUWLP-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0218613.8 | 2002-08-10 | ||
| GBGB0218613.8A GB0218613D0 (en) | 2002-08-10 | 2002-08-10 | Process for the carbonylation of ethylenically unsaturated compounds |
| GB0228018.8 | 2002-11-30 | ||
| GBGB0228018.8A GB0228018D0 (en) | 2002-11-30 | 2002-11-30 | Carbonylation of ester |
| GB0316159A GB0316159D0 (en) | 2003-07-10 | 2003-07-10 | A catalyst system |
| GB0316159.3 | 2003-07-10 | ||
| PCT/GB2003/003419 WO2004014552A1 (en) | 2002-08-10 | 2003-08-06 | A phospha-adamantane (s) catalytic system |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005535455A JP2005535455A (ja) | 2005-11-24 |
| JP2005535455A5 true JP2005535455A5 (enExample) | 2007-05-17 |
| JP5101014B2 JP5101014B2 (ja) | 2012-12-19 |
Family
ID=31721066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005506118A Expired - Fee Related JP5101014B2 (ja) | 2002-08-10 | 2003-08-06 | ホスファアダマンタン触媒系、及びその触媒系を用いたエチレン性不飽和化合物のカルボニル化の方法 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7371705B2 (enExample) |
| EP (1) | EP1534427B1 (enExample) |
| JP (1) | JP5101014B2 (enExample) |
| KR (1) | KR101035697B1 (enExample) |
| CN (1) | CN1674990B (enExample) |
| AT (1) | ATE446140T1 (enExample) |
| AU (1) | AU2003259322C1 (enExample) |
| BR (1) | BR0313289B1 (enExample) |
| CA (1) | CA2493250C (enExample) |
| DE (1) | DE60329764D1 (enExample) |
| ES (1) | ES2334222T3 (enExample) |
| IN (1) | IN227859B (enExample) |
| MY (1) | MY139539A (enExample) |
| PL (1) | PL374194A1 (enExample) |
| TW (1) | TWI301481B (enExample) |
| WO (1) | WO2004014552A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1651587A1 (en) | 2003-07-03 | 2006-05-03 | Lucite International UK Limited | Process for the hydroformylation of ethylenically unsaturated compounds |
| GB0403592D0 (en) | 2004-02-18 | 2004-03-24 | Lucite Int Uk Ltd | A catalyst system |
| GB0411951D0 (en) * | 2004-05-28 | 2004-06-30 | Lucite Int Uk Ltd | Carbonylation of ester |
| GB0516556D0 (en) * | 2005-08-12 | 2005-09-21 | Lucite Int Uk Ltd | Improved catalyst system |
| ES2700427T3 (es) | 2005-11-17 | 2019-02-15 | Lucite Int Uk Ltd | Carbonilación de compuestos etilénicamente insaturados |
| GB0607494D0 (en) | 2006-04-13 | 2006-05-24 | Lucite Int Uk Ltd | Metal complexes |
| GB2437930A (en) * | 2006-05-10 | 2007-11-14 | Lucite Int Uk Ltd | Mixing apparatus |
| WO2008065448A1 (en) * | 2006-12-02 | 2008-06-05 | Lucite International Uk Limited | Novel carbonylation ligands and their use in the carbonylation of ethylenically unsaturated compounds |
| GB0625518D0 (en) * | 2006-12-21 | 2007-01-31 | Lucite Int Uk Ltd | Carbonylation of conjugated dienes |
| GB0812297D0 (en) | 2008-07-04 | 2008-08-13 | Lucite Int Uk Ltd | Novel carbonylation ligand sand thier use of in the carbonylation of ethylenically unsaturated compounds |
| GB201000078D0 (en) * | 2010-01-05 | 2010-02-17 | Lucite Int Uk Ltd | Process for the carbonylation of ethylenically unsaturated compounds, novel carbonylation ligands and catalyst systems incorporatng such ligands |
| WO2016164258A1 (en) * | 2015-04-10 | 2016-10-13 | Dow Global Technologies Llc | Butadiene telomerization catalyst and preparation thereof |
| EP3441384B1 (de) * | 2017-08-08 | 2019-12-25 | Evonik Operations GmbH | Methoxycarbonylierung mit ameisensäure und methanol |
| EP3441383B1 (de) * | 2017-08-08 | 2019-12-25 | Evonik Operations GmbH | Methoxycarbonylierung mit ameisensäure als co-quelle |
| CN111087306B (zh) | 2019-12-27 | 2021-08-03 | 南京诚志清洁能源有限公司 | 芳基双齿膦配体组合催化制备有机羧酸酯的方法 |
| CN113999262B (zh) * | 2021-12-31 | 2022-03-29 | 苏州欣诺科生物科技有限公司 | 二(1-金刚烷基)环烷基膦配体的制备方法 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4377708A (en) | 1977-10-14 | 1983-03-22 | Monsanto Company | Hydrocarboxylation of vinyl alkanoates |
| DE2824010A1 (de) | 1978-06-01 | 1979-12-13 | Metallgesellschaft Ag | Verfahren zur aufkonzentrierung von verduennter phosphorsaeure |
| EP0055875B1 (en) | 1981-01-06 | 1986-08-20 | Shell Internationale Researchmaatschappij B.V. | Process for the carbonylation of olefins |
| CA1231346A (en) | 1982-09-30 | 1988-01-12 | Eit Drent | Process for the carbonylation of olefinically unsaturated compounds with a palladium catalyst |
| GB8531624D0 (en) | 1985-12-23 | 1986-02-05 | Shell Int Research | Carbonylation of ethylenically unsaturated compounds |
| GB8605034D0 (en) | 1986-02-28 | 1986-04-09 | Shell Int Research | Carbonylation of compounds |
| KR880007426A (ko) | 1986-12-24 | 1988-08-27 | 오노 알버어스 | 팔라듐 촉매를 사용한 올레핀형 불포화 화합물의 카르보닐화 방법 |
| GB8705699D0 (en) | 1987-03-11 | 1987-04-15 | Shell Int Research | Carbonylation of olefinically unsaturated compounds |
| US4960949A (en) * | 1988-12-22 | 1990-10-02 | Eastman Kodak Company | Low pressure rhodium catalyzed hydroformylation of olefins |
| KR0144567B1 (ko) | 1989-03-03 | 1998-07-15 | 오노 알버어스 | 카르보닐화촉매시스템 |
| CA2034971A1 (en) | 1990-02-05 | 1991-08-06 | Eit Drent | Carbonylation catalyst system |
| CA2055628A1 (en) | 1990-12-03 | 1992-06-04 | Eit Drent | Carbonylation process and catalyst composition |
| DE69204691T2 (de) | 1991-01-15 | 1996-04-11 | Shell Int Research | Verfahren zur Karbonylierung von Olefin. |
| ES2088082T3 (es) | 1991-01-15 | 1996-08-01 | Shell Int Research | Carbonilacion de olefinas. |
| ES2054519T3 (es) | 1991-02-15 | 1994-08-01 | Shell Int Research | Sistema de catalizador de carbonilacion. |
| GB9425911D0 (en) | 1994-12-22 | 1995-02-22 | Ici Plc | Process for the carbonylation of olefins and catalyst system for use therein |
| GB9705699D0 (en) | 1997-03-19 | 1997-05-07 | Ici Plc | Process for the carbonylation of ethylene |
| GB9717059D0 (en) | 1997-08-13 | 1997-10-15 | Ici Plc | Method of manufacturing phosphine compound |
| GB9722733D0 (en) | 1997-10-29 | 1998-10-28 | Ici Plc | Production of esters |
| GB9805348D0 (en) | 1998-03-16 | 1998-05-06 | Ici Plc | Compound |
| GB9918229D0 (en) * | 1999-08-04 | 1999-10-06 | Ici Plc | Improvements relating to metal-compound catalysed processes |
| MY127358A (en) | 2000-03-14 | 2006-11-30 | Shell Int Research | Process for the carbonylation of ethylenically unsaturated compounds |
| MY133839A (en) | 2000-03-14 | 2007-11-30 | Shell Int Research | Process for the carbonylation of pentenenitrile |
| EP1478463B1 (en) * | 2002-02-19 | 2012-04-11 | Lucite International UK Limited | Process for the carbonylation of an ethylenically unsaturated compound and catalyst therefore |
| EP1651587A1 (en) | 2003-07-03 | 2006-05-03 | Lucite International UK Limited | Process for the hydroformylation of ethylenically unsaturated compounds |
-
2003
- 2003-07-29 TW TW092120692A patent/TWI301481B/zh not_active IP Right Cessation
- 2003-08-06 KR KR1020057002048A patent/KR101035697B1/ko not_active Expired - Fee Related
- 2003-08-06 US US10/524,023 patent/US7371705B2/en not_active Expired - Lifetime
- 2003-08-06 PL PL03374194A patent/PL374194A1/xx unknown
- 2003-08-06 EP EP03784257A patent/EP1534427B1/en not_active Expired - Lifetime
- 2003-08-06 AT AT03784257T patent/ATE446140T1/de not_active IP Right Cessation
- 2003-08-06 IN IN333DE2005 patent/IN227859B/en unknown
- 2003-08-06 BR BRPI0313289-7A patent/BR0313289B1/pt not_active IP Right Cessation
- 2003-08-06 WO PCT/GB2003/003419 patent/WO2004014552A1/en not_active Ceased
- 2003-08-06 JP JP2005506118A patent/JP5101014B2/ja not_active Expired - Fee Related
- 2003-08-06 AU AU2003259322A patent/AU2003259322C1/en not_active Ceased
- 2003-08-06 ES ES03784257T patent/ES2334222T3/es not_active Expired - Lifetime
- 2003-08-06 DE DE60329764T patent/DE60329764D1/de not_active Expired - Lifetime
- 2003-08-06 CA CA2493250A patent/CA2493250C/en not_active Expired - Fee Related
- 2003-08-06 CN CN038190796A patent/CN1674990B/zh not_active Expired - Lifetime
- 2003-08-08 MY MYPI20033011A patent/MY139539A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2005535455A5 (enExample) | ||
| Fischer et al. | Silylgermylpotassium compounds | |
| JPH04275294A (ja) | リガンドとして二環シクロペンタジエン誘導体を持つメタロセン、その製造方法およびそれの触媒としての用途 | |
| US6043403A (en) | Process for the preparation of cyclopentadienyl compounds and compounds obtained therefrom | |
| Guthardt et al. | Planar-chiral 1, 1′-diaminoferrocenes | |
| US4447628A (en) | Nonhygroscopic, anionic pentacoordinate silicate | |
| Liau et al. | Oligomerization of digoldacetylide complexes through angular head-to-tail aurophilic bonding | |
| Clark et al. | Compounds with ruthenium-silicon and osmium-silicon bonds | |
| Miguel-Garcia et al. | Ring-methyl activation in pentamethylcyclopentadienyliridium complexes; synthesis of [(C5Me4CH2E) IrLn](E= SiMe3, PhCH2, CH2= CHCH2, PPh2, and Pt (PEt3) 2Cl), and synthesis and X-ray structure of [(1, 3-C5Me3 (CH2SiMe3) 2) Ir (CO) Me (Cl)] | |
| Beşli et al. | Single-, double-and triple-bridged derivatives of cyclotriphosphazenes with an octafluorohexane-1, 6-diol | |
| Pampillón et al. | Diheteroarylmethyl substituted titanocenes: a novel class of possible anti-cancer drugs | |
| Burchell et al. | Organogold (I) complexes of a C2-symmetric diacetylide ligand derived from 1, 1′-bi-2-naphthol | |
| Sweeney et al. | The synthesis and cytotoxic evaluation of a series of benzodioxole substituted titanocenes | |
| EP0442097B1 (de) | Poly (arylenvinylen-siloxane) | |
| US4632967A (en) | Nonhygroscopic, anionic pentacoordinate silicate | |
| Reuter et al. | Synthesis of heteroatomic bridged paracyclophanes | |
| Young et al. | Synthesis, structure determinations, and reduction of (C5H5) 2Zr (Cl) CH2PMe2 and (C5Me5) 2Zr (Cl) CH2PPh2 | |
| Fuchita et al. | Metallation of aliphatic carbon atoms. Part 5. Synthesis and characterization of the cyclopalladated complexes of 2-(trimethylsilyl) pyridine and their dynamic behaviour observed by proton nuclear magnetic resonance spectroscopy | |
| DeHope et al. | A persistent (amino)(ferrocenyl) carbene | |
| Liu et al. | Synthesis and structures of cyclopentadienyl fluoro and chloro complexes of a triad (Ti, Zr, Hf) containing acyclic and cyclic siloxane building blocks | |
| EP3621969B1 (de) | Cupratverbindungen sowie verfahren zu deren herstellung und anwendungsmöglichkeiten | |
| Shibley et al. | Synthesis of an azadisilacyclopropane and two cyclodisilazanes from 1, 1, 2, 2-tetrachloro-1, 2-dimesityldisilane | |
| Dorado et al. | Regioselective formation of [2-(η5-cyclopentadienyl)-2-fluorenylpropane]-titanium complexes: precursors, synthesis, structure and reactivity | |
| DE19632919A1 (de) | Katalysatorsystem | |
| Segerer et al. | Formation of novel P-functionalised ligands by insertion of CyNC into the Zr P bonds of [Cp° 2ZrCl (PHCy)](Cp°= η5-C5EtMe4, Cy= cyclohexyl) and [Cp′ 2ZrCl (PHTipp)](Cp′= η5-C5H4Me, Tipp= 2, 4, 6-Pri3C6H2). Molecular structures of [Cp° 2ZrCl {η2-NCyC (PHCy)}] and [Cp′ 2Zr (Cl){η2-NCyC (PHTipp)}] |