JP2003509515A5 - - Google Patents
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- JP2003509515A5 JP2003509515A5 JP2001525002A JP2001525002A JP2003509515A5 JP 2003509515 A5 JP2003509515 A5 JP 2003509515A5 JP 2001525002 A JP2001525002 A JP 2001525002A JP 2001525002 A JP2001525002 A JP 2001525002A JP 2003509515 A5 JP2003509515 A5 JP 2003509515A5
- Authority
- JP
- Japan
- Prior art keywords
- independently
- alkyl
- aryl
- cho
- formula
- 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
- 125000000217 alkyl group Chemical group 0.000 description 54
- 125000003118 aryl group Chemical group 0.000 description 54
- 239000003446 ligand Substances 0.000 description 18
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 229910052703 rhodium Inorganic materials 0.000 description 11
- 239000010948 rhodium Substances 0.000 description 11
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 8
- -1 organic acid salt Chemical class 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- UVKXJAUUKPDDNW-NSCUHMNNSA-N (e)-pent-3-enenitrile Chemical compound C\C=C\CC#N UVKXJAUUKPDDNW-NSCUHMNNSA-N 0.000 description 3
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 3
- CFEYBLWMNFZOPB-UHFFFAOYSA-N Allylacetonitrile Natural products C=CCCC#N CFEYBLWMNFZOPB-UHFFFAOYSA-N 0.000 description 3
- 125000002015 acyclic group Chemical group 0.000 description 3
- 238000007037 hydroformylation reaction Methods 0.000 description 3
- 150000001299 aldehydes Chemical group 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 150000001728 carbonyl compounds Chemical class 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- WUCQRXWCJPCWTQ-NSCUHMNNSA-N (e)-pent-3-enal Chemical compound C\C=C\CC=O WUCQRXWCJPCWTQ-NSCUHMNNSA-N 0.000 description 1
- PNPPVRALIYXJBW-UHFFFAOYSA-N 6-oxohexanoic acid Chemical compound OC(=O)CCCCC=O PNPPVRALIYXJBW-UHFFFAOYSA-N 0.000 description 1
- 0 COc(c(*)c(*)c1c2c(*)c(*)c(S)c1*)c2-c(c1c(c(*)c2*)c(*)c(*)c(S)c1*)c2OC Chemical compound COc(c(*)c(*)c1c2c(*)c(*)c(S)c1*)c2-c(c1c(c(*)c2*)c(*)c(*)c(S)c1*)c2OC 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- KJALUUCEMMPKAC-ONEGZZNKSA-N methyl (e)-pent-3-enoate Chemical compound COC(=O)C\C=C\C KJALUUCEMMPKAC-ONEGZZNKSA-N 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- WUCQRXWCJPCWTQ-UHFFFAOYSA-N trans-3-pentenal Natural products CC=CCC=O WUCQRXWCJPCWTQ-UHFFFAOYSA-N 0.000 description 1
- UIUWNILCHFBLEQ-NSCUHMNNSA-N trans-pent-3-enoic acid Chemical compound C\C=C\CC(O)=O UIUWNILCHFBLEQ-NSCUHMNNSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/399,252 US6307107B1 (en) | 1999-09-20 | 1999-09-20 | Hydroformylation of acyclic monoethylenically unsaturated compounds to corresponding terminal aldehydes |
| US09/399,252 | 1999-09-20 | ||
| PCT/US2000/025122 WO2001021627A1 (en) | 1999-09-20 | 2000-09-14 | Hydroformylation using multidentate phosphite ligands |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003509515A JP2003509515A (ja) | 2003-03-11 |
| JP2003509515A5 true JP2003509515A5 (enExample) | 2007-10-04 |
Family
ID=23578804
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001525002A Pending JP2003509515A (ja) | 1999-09-20 | 2000-09-14 | 多座ホスファイト配位子を用いるヒドロホルミル化 |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US6307107B1 (enExample) |
| EP (1) | EP1216252B1 (enExample) |
| JP (1) | JP2003509515A (enExample) |
| KR (1) | KR100644303B1 (enExample) |
| CN (1) | CN1145633C (enExample) |
| AU (1) | AU7378200A (enExample) |
| BR (1) | BR0014572A (enExample) |
| CA (1) | CA2380626C (enExample) |
| CZ (1) | CZ2002955A3 (enExample) |
| DE (1) | DE60006561T2 (enExample) |
| MX (1) | MXPA02002988A (enExample) |
| PL (1) | PL202488B1 (enExample) |
| SK (1) | SK3932002A3 (enExample) |
| TW (1) | TW581769B (enExample) |
| WO (1) | WO2001021627A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6653485B2 (en) * | 2000-11-17 | 2003-11-25 | The Penn State Research Foundation | Ortho substituted chiral phosphines and phosphinites and their use in asymmetric catalytic reactions |
| CN1289539C (zh) | 2001-11-26 | 2006-12-13 | 因维斯塔技术有限公司 | 载体上的双(磷)配体及其在催化中的应用 |
| US6750362B2 (en) * | 2002-03-12 | 2004-06-15 | E. I. Du Pont De Nemours And Company | Process for making 5-formylvaleronitrile using reactivated catalyst |
| AU2003253389A1 (en) | 2002-08-31 | 2004-03-19 | Oxeno Olefinchemie Gmbh | Method for the hydroformylation of olefinically unsaturated compounds, especially olefins, in the presence of cyclic carbonic acid esters |
| JP4328080B2 (ja) * | 2002-10-30 | 2009-09-09 | 三菱化学株式会社 | 固体担持有機リン化合物、遷移金属錯体、及び触媒反応方法 |
| US6906218B2 (en) | 2002-12-18 | 2005-06-14 | Invista North America S.A.R.L. | Cyclohexane derivatives and methods for their preparation |
| FR2849027B1 (fr) * | 2002-12-23 | 2005-01-21 | Rhodia Polyamide Intermediates | Procede de synthese de composes comprenant des fonctions nitriles a partir de composes a insaturations ethyleniques |
| US6936171B2 (en) * | 2003-01-08 | 2005-08-30 | Invista North America S.A.R.L. | Process for catalyst recovery from hydrocyanation product mixtures |
| US6897329B2 (en) * | 2003-01-14 | 2005-05-24 | Invista North America S.A.R.L. | Process for the preparation of nickel/phosphorous ligand catalyst for olefin hydrocyanation |
| FR2850966B1 (fr) | 2003-02-10 | 2005-03-18 | Rhodia Polyamide Intermediates | Procede de fabrication de composes dinitriles |
| US6844289B2 (en) * | 2003-04-08 | 2005-01-18 | Invista North America S.A.R.L. | Process for the preparation of a nickel/phosphorous ligand catalyst |
| FR2854891B1 (fr) | 2003-05-12 | 2006-07-07 | Rhodia Polyamide Intermediates | Procede de preparation de dinitriles |
| FR2854892B1 (fr) * | 2003-05-12 | 2005-06-24 | Rhodia Polyamide Intermediates | Procede de fabrication de dinitriles |
| EP2154127A3 (en) | 2003-09-11 | 2010-10-13 | Invista Technologies S.à.r.l. | Conversion of hydrocyanated unsaturated carboxylic acid derivatives into amines |
| US8119829B2 (en) * | 2004-09-08 | 2012-02-21 | Invista North America S.A.R.L. | Process of hydrocyanation of unsaturated carboxylic acid derivatives |
| CA2647396C (en) | 2006-03-17 | 2014-01-07 | University Of Kansas | Tuning product selectivity in catalytic hydroformylation reactions with carbon dioxide expanded liquids |
| JP2009530278A (ja) * | 2006-03-17 | 2009-08-27 | インビスタ テクノロジーズ エス エイ アール エル | 塩基性添加剤による処理でトリ有機ホスファイトを精製する方法 |
| US7709674B2 (en) * | 2006-07-14 | 2010-05-04 | Invista North America S.A R.L | Hydrocyanation process with reduced yield losses |
| US7586010B2 (en) * | 2006-12-21 | 2009-09-08 | Eastman Chemical Company | Phosphonite-containing catalysts for hydroformylation processes |
| CA2743720C (en) | 2008-11-14 | 2019-03-12 | University Of Kansas | Polymer-supported transition metal catalyst complexes and methods of use |
| CN103402595B (zh) | 2011-12-21 | 2016-02-03 | 因温斯特技术公司 | 用于减少稳定乳液的萃取溶剂控制 |
| KR20140127218A (ko) | 2011-12-21 | 2014-11-03 | 인비스타 테크놀러지스 에스.에이 알.엘. | 안정한 에멀젼을 감소시키기 위한 추출 용매 제어 |
| KR20140108683A (ko) | 2011-12-21 | 2014-09-12 | 인비스타 테크놀러지스 에스.에이 알.엘. | 안정한 에멀젼을 감소시키기 위한 추출 용매 제어 |
| HK1199630A1 (en) | 2011-12-21 | 2015-07-10 | 因温斯特技术公司 | Extraction solvent control for reducing stable emulsions |
| CN105431405B (zh) * | 2013-03-14 | 2018-06-01 | 澳门大学 | 分离自益智仁的新抗神经变性天然化合物及其全合成 |
| DE102014201756A1 (de) | 2014-01-31 | 2015-08-06 | Evonik Degussa Gmbh | Reinigung chlorverschmutzter Organophosphorverbindungen |
| US9914700B2 (en) | 2014-06-27 | 2018-03-13 | Invista North America S.A R.L. | Enhanced extraction of impurities from mixture comprising nitriles |
| US10035756B2 (en) | 2014-06-27 | 2018-07-31 | Invista North America S.A.R.L. | Integrated process for nitrile manufacture with enhanced liquid-liquid extraction |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4885401A (en) | 1985-09-05 | 1989-12-05 | Union Carbide Corporation | Bis-phosphite compounds |
| US4668651A (en) | 1985-09-05 | 1987-05-26 | Union Carbide Corporation | Transition metal complex catalyzed processes |
| US5113022A (en) | 1988-08-05 | 1992-05-12 | Union Carbide Chemicals & Plastics Technology Corporation | Ionic phosphites used in homogeneous transition metal catalyzed processes |
| US5059710A (en) | 1988-08-05 | 1991-10-22 | Union Carbide Chemicals And Plastics Technology Corporation | Ionic phosphites and their use in homogeneous transition metal catalyzed processes |
| TW213465B (enExample) | 1991-06-11 | 1993-09-21 | Mitsubishi Chemicals Co Ltd | |
| US5360938A (en) | 1991-08-21 | 1994-11-01 | Union Carbide Chemicals & Plastics Technology Corporation | Asymmetric syntheses |
| DE4204808A1 (de) | 1992-02-18 | 1993-08-19 | Basf Ag | Verfahren zur herstellung von (omega)-formylalkancarbonsaeureestern |
| BE1007944A3 (nl) | 1993-12-30 | 1995-11-21 | Dsm Nv | Werkwijze voor de bereiding van 5-formylvaleriaanzuur en -ester. |
| JPH0977713A (ja) * | 1995-09-19 | 1997-03-25 | Mitsubishi Chem Corp | アルデヒド類の製造方法 |
| TW343195B (en) * | 1996-03-15 | 1998-10-21 | Dsm Nv | Process to prepare a terminal aldehyde |
| US5874641A (en) * | 1996-03-15 | 1999-02-23 | Dsm N.V. | Process to prepare a terminal aldehyde |
| EP0839787A1 (en) * | 1996-11-04 | 1998-05-06 | Dsm N.V. | Process for the preparation of an aldehyde |
| DE19717359B4 (de) * | 1996-04-30 | 2014-10-30 | Mitsubishi Chemical Corp. | Bisphosphitverbindungen und Verfahren zu deren Herstellung |
| ZA986369B (en) * | 1997-07-29 | 2000-01-17 | Du Pont | Hydrocyanation of diolefins and isomerization of nonconjugated 2-alkyl-3-monoalkenenitriles. |
| US5952530A (en) * | 1998-02-02 | 1999-09-14 | Union Carbide Chemicals & Plastics Technology Corporation | Separation processes |
| WO2001021580A1 (en) * | 1999-09-20 | 2001-03-29 | E.I. Du Pont De Nemours And Company | Multidentate phosphite ligands, catalytic compositions containing such ligands and catalytic processes utilizing such catalytic compositions |
-
1999
- 1999-09-20 US US09/399,252 patent/US6307107B1/en not_active Expired - Lifetime
-
2000
- 2000-09-14 DE DE60006561T patent/DE60006561T2/de not_active Expired - Lifetime
- 2000-09-14 CA CA002380626A patent/CA2380626C/en not_active Expired - Fee Related
- 2000-09-14 MX MXPA02002988A patent/MXPA02002988A/es active IP Right Grant
- 2000-09-14 KR KR1020027003630A patent/KR100644303B1/ko not_active Expired - Fee Related
- 2000-09-14 CN CNB008131244A patent/CN1145633C/zh not_active Expired - Fee Related
- 2000-09-14 EP EP00961890A patent/EP1216252B1/en not_active Expired - Lifetime
- 2000-09-14 PL PL354967A patent/PL202488B1/pl not_active IP Right Cessation
- 2000-09-14 SK SK393-2002A patent/SK3932002A3/sk unknown
- 2000-09-14 AU AU73782/00A patent/AU7378200A/en not_active Abandoned
- 2000-09-14 WO PCT/US2000/025122 patent/WO2001021627A1/en not_active Ceased
- 2000-09-14 JP JP2001525002A patent/JP2003509515A/ja active Pending
- 2000-09-14 CZ CZ2002955A patent/CZ2002955A3/cs unknown
- 2000-09-14 BR BR0014572-6A patent/BR0014572A/pt not_active Application Discontinuation
- 2000-09-29 TW TW089119365A patent/TW581769B/zh not_active IP Right Cessation
-
2001
- 2001-07-26 US US09/916,129 patent/US6399534B2/en not_active Expired - Lifetime
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