JP2002516891A5 - - Google Patents
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- Publication number
- JP2002516891A5 JP2002516891A5 JP2000552070A JP2000552070A JP2002516891A5 JP 2002516891 A5 JP2002516891 A5 JP 2002516891A5 JP 2000552070 A JP2000552070 A JP 2000552070A JP 2000552070 A JP2000552070 A JP 2000552070A JP 2002516891 A5 JP2002516891 A5 JP 2002516891A5
- Authority
- JP
- Japan
- Prior art keywords
- method described
- alkyl
- aryl
- aryloxy
- alkoxy
- 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
- 238000000034 method Methods 0.000 description 29
- 125000003118 aryl group Chemical group 0.000 description 16
- 125000000217 alkyl group Chemical group 0.000 description 14
- 125000004104 aryloxy group Chemical group 0.000 description 14
- 125000003545 alkoxy group Chemical group 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 10
- 229910002091 carbon monoxide Inorganic materials 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- 125000002015 acyclic group Chemical group 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 group [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000012634 fragment Substances 0.000 description 6
- 238000007037 hydroformylation reaction Methods 0.000 description 6
- -1 acyclic aromatic olefin compound Chemical class 0.000 description 4
- 229920000620 organic polymer Polymers 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000002952 polymeric resin Substances 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 0 CO*(*)O*N* Chemical compound CO*(*)O*N* 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 150000003284 rhodium compounds Chemical class 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- LNQFKNCJGVGEGA-UHFFFAOYSA-N [Rh+6].[O-]P([O-])[O-].[O-]P([O-])[O-] Chemical compound [Rh+6].[O-]P([O-])[O-].[O-]P([O-])[O-] LNQFKNCJGVGEGA-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- UIUWNILCHFBLEQ-NSCUHMNNSA-N trans-pent-3-enoic acid Chemical compound C\C=C\CC(O)=O UIUWNILCHFBLEQ-NSCUHMNNSA-N 0.000 description 2
- PPTXVXKCQZKFBN-UHFFFAOYSA-N (S)-(-)-1,1'-Bi-2-naphthol Chemical group C1=CC=C2C(C3=C4C=CC=CC4=CC=C3O)=C(O)C=CC2=C1 PPTXVXKCQZKFBN-UHFFFAOYSA-N 0.000 description 1
- UVKXJAUUKPDDNW-NSCUHMNNSA-N (e)-pent-3-enenitrile Chemical compound C\C=C\CC#N UVKXJAUUKPDDNW-NSCUHMNNSA-N 0.000 description 1
- ZDZHCHYQNPQSGG-UHFFFAOYSA-N 1-naphthalen-1-ylnaphthalene Chemical group C1=CC=C2C(C=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 ZDZHCHYQNPQSGG-UHFFFAOYSA-N 0.000 description 1
- CFEYBLWMNFZOPB-UHFFFAOYSA-N Allylacetonitrile Natural products C=CCCC#N CFEYBLWMNFZOPB-UHFFFAOYSA-N 0.000 description 1
- SHCSFZHSNSGTOP-UHFFFAOYSA-N Methyl 4-pentenoate Chemical compound COC(=O)CCC=C SHCSFZHSNSGTOP-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 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
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-N pent-4-enoic acid Chemical compound OC(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-N 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 125000005106 triarylsilyl group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8715198P | 1998-05-29 | 1998-05-29 | |
| US60/087,151 | 1998-05-29 | ||
| PCT/US1999/011557 WO1999062855A1 (en) | 1998-05-29 | 1999-05-26 | Hydroformylation of olefins using supported bis(phosphorus) ligands |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002516891A JP2002516891A (ja) | 2002-06-11 |
| JP2002516891A5 true JP2002516891A5 (enExample) | 2006-06-29 |
| JP4309057B2 JP4309057B2 (ja) | 2009-08-05 |
Family
ID=22203407
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000552070A Expired - Fee Related JP4309057B2 (ja) | 1998-05-29 | 1999-05-26 | 担持されたビス（リン）配位子を用いるオレフィンのヒドロホルミル化 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US6229052B1 (enExample) |
| EP (1) | EP1082285B1 (enExample) |
| JP (1) | JP4309057B2 (enExample) |
| KR (1) | KR100580420B1 (enExample) |
| AT (1) | ATE271532T1 (enExample) |
| BR (1) | BR9911205A (enExample) |
| CA (1) | CA2330153A1 (enExample) |
| DE (1) | DE69918828T2 (enExample) |
| ES (1) | ES2224669T3 (enExample) |
| ID (1) | ID26775A (enExample) |
| MY (1) | MY121451A (enExample) |
| TW (1) | TWI253448B (enExample) |
| WO (1) | WO1999062855A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6420611B1 (en) * | 1999-09-20 | 2002-07-16 | E. I. Du Pont De Nemours And Company | Composition comprising polymeric phosphite |
| JP2001139691A (ja) * | 1999-11-16 | 2001-05-22 | Mitsubishi Chemicals Corp | ３価リン含有重合体触媒によるアルデヒド類の製造方法および新規なホスファイト含有重合体 |
| DE10002976A1 (de) * | 2000-01-24 | 2001-07-26 | Degussa | Molekulargewichtsvergrößerte Liganden für asymmetrische homogen lösliche Hydrierkatalysatoren, Verfahren zu deren Herstellung und Verwendung |
| WO2002040573A1 (fr) * | 2000-11-17 | 2002-05-23 | Mitsubishi Rayon Co., Ltd. | Binaphtyles optiquement actifs a support solide et procede de preparation de derives d'aminonitrile asymetriques a l'aide de ceux-ci |
| JP4796235B2 (ja) * | 2001-03-27 | 2011-10-19 | 上野製薬株式会社 | ビナフトール誘導体金属塩およびその製法 |
| US6660876B2 (en) | 2001-11-26 | 2003-12-09 | E. I. Du Pont De Nemours And Company | Phosphorus-containing compositions and their use in hydrocyanation, isomerization and hydroformylation reactions |
| ES2307808T3 (es) | 2001-11-26 | 2008-12-01 | Invista Technologies S.A.R.L. | Ligandos bis(fosforo) soportados y su uso en la catalisis. |
| US20030100803A1 (en) | 2001-11-26 | 2003-05-29 | Lu Helen S.M. | 3-Alkylated-5,5',6,6',7,7,'8,8'-octahydro-2,2'-binaphthols and 3,3'-dialkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and processes for making them |
| US20030135014A1 (en) * | 2001-11-26 | 2003-07-17 | Radu Nora S. | Polymeric, phosphorus-containing compositions and their use in hydrocyanation, isomerization and hydroformylation reactions |
| US6664427B1 (en) * | 2002-08-29 | 2003-12-16 | E. I. Du Pont De Nemours And Company | Process for preparing aldehyde compounds |
| 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 |
| DE10349343A1 (de) * | 2003-10-23 | 2005-06-02 | Basf Ag | Stabilisierung von Hydroformylierungskatalysatoren auf Basis von Phosphoramiditliganden |
| DE102004033575B3 (de) | 2004-07-09 | 2006-04-13 | Schunk Ultraschalltechnik Gmbh | Anordnung zum Verschweißen von Werkstücken |
| US20060258875A1 (en) * | 2005-05-10 | 2006-11-16 | Clementine Reyes | Methods for manufacturing supported nanocatalysts and methods for using supported nanocatalysts |
| US8097229B2 (en) * | 2006-01-17 | 2012-01-17 | Headwaters Technology Innovation, Llc | Methods for manufacturing functionalized inorganic oxides and polymers incorporating same |
| US7943061B2 (en) * | 2006-04-10 | 2011-05-17 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Chiral binaphthyl sulfates for use as liquid crystal materials |
| JP4020155B2 (ja) * | 2006-07-31 | 2007-12-12 | 三菱化学株式会社 | 有機二リン基架橋型重合体 |
| FR2926816B1 (fr) | 2008-01-25 | 2010-05-14 | Rhodia Operations | Procede de fabrication de composes comprenant des fonctions nitriles |
| FR2932477B1 (fr) | 2008-06-17 | 2013-01-18 | Rhodia Operations | Procede de fabrication de composes nitriles a partir de composes a insaturation ethylenique |
| FR2937321B1 (fr) | 2008-10-21 | 2010-10-22 | Rhodia Operations | Procede de fabrication de composes comprenant des fonctions nitriles |
| WO2010057099A1 (en) | 2008-11-14 | 2010-05-20 | University Of Kansas | Polymer-supported transition metal catalyst complexes and methods of use |
| FR2941455B1 (fr) | 2009-01-29 | 2011-02-11 | Rhodia Operations | Procede de fabrication de composes comprenant des fonctions nitriles |
| JP5823967B2 (ja) * | 2009-10-16 | 2015-11-25 | ダウ テクノロジー インベストメンツ リミティド ライアビリティー カンパニー | 気相ヒドロホルミル化方法 |
| JP5932556B2 (ja) * | 2012-08-07 | 2016-06-08 | 富士フイルム株式会社 | 液晶組成物、高分子、フィルムおよびコレステリック液晶 |
| JP6109604B2 (ja) * | 2013-03-05 | 2017-04-05 | 嶋田 豊司 | オクタヒドロビナフチル誘導体 |
| US9611203B2 (en) | 2013-12-11 | 2017-04-04 | Dalian Institute Of Chemical Physics, Chinese Academy Of Sciences | Method for olefin hydroformylation reaction using solid heterogeneous catalyst |
| JP6867303B2 (ja) | 2015-12-25 | 2021-04-28 | 東洋合成工業株式会社 | 化合物及び有機材料の製造方法 |
| CN109942750B (zh) * | 2019-01-14 | 2021-06-25 | 青岛科技大学 | 含有双齿亚磷酰胺配体的多孔有机聚合物及其制备方法和应用 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3496215A (en) | 1965-11-23 | 1970-02-17 | Du Pont | Hydrocyanation of olefins using selected nickel phosphite catalysts |
| US3655723A (en) | 1969-10-31 | 1972-04-11 | Du Pont | Hydrocyanation of olefins |
| US3631191A (en) | 1970-04-08 | 1971-12-28 | Du Pont | Synthesis of zero valent nickel-tetrakis triaryl phosphite complexes |
| US3766237A (en) | 1972-01-25 | 1973-10-16 | Du Pont | Hydrocyanation of olefins |
| FR2408388A1 (fr) * | 1977-11-10 | 1979-06-08 | Ugine Kuhlmann | Complexe binucleaire du rhodium en tant que catalyseur d'hydroformylation et d'hydrogenation |
| NL8003059A (nl) | 1980-05-28 | 1982-01-04 | Stamicarbon | Werkwijze en katalysator voor het uitvoeren van hydroformyleringsreacties. |
| US4947003A (en) * | 1988-11-28 | 1990-08-07 | Virginia Tech Intellectual Properties, Inc. | Process for the hydroformulation of olefinically unsaturated organic reactants using a supported aqueous phase catalyst |
| EP0496700B1 (de) | 1991-01-25 | 1996-03-06 | Ciba-Geigy Ag | Silangruppen enthaltende Diphosphine, immobilisierte Diophoshine und deren Verwendung als Hydrierkatalysatoren |
| 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 |
| US5288918A (en) * | 1992-09-29 | 1994-02-22 | Union Carbide Chemicals & Plastics Technology Corporation | Hydroformylation process |
| KR100263138B1 (ko) | 1993-11-23 | 2000-08-01 | 이.아이,듀우판드네모아앤드캄파니 | 모노올레핀의 하이드로시안화 방법 및 이를 위한 촉매 조성물 |
| BE1008017A3 (nl) * | 1994-01-06 | 1995-12-12 | Dsm Nv | Werkwijze voor de bereiding van 5-formylvaleriaanzure ester. |
| US5512695A (en) | 1994-04-14 | 1996-04-30 | E. I. Du Pont De Nemours And Company | Bidentate phosphite and nickel catalyst compositions for hydrocyanation of monoolefins |
| US5512696A (en) | 1995-07-21 | 1996-04-30 | E. I. Du Pont De Nemours And Company | Hydrocyanation process and multidentate phosphite and nickel catalyst composition therefor |
| TW343195B (en) | 1996-03-15 | 1998-10-21 | Dsm Nv | Process to prepare a terminal aldehyde |
| EP0839787A1 (en) * | 1996-11-04 | 1998-05-06 | Dsm N.V. | Process for the preparation of an aldehyde |
| US5710344A (en) | 1996-11-08 | 1998-01-20 | E. I. Du Pont De Nemours And Company | Process to prepare a linear aldehyde |
| JP3892931B2 (ja) | 1997-03-11 | 2007-03-14 | 高砂香料工業株式会社 | ２個のビニル基を有する光学活性ホスフィン誘導体、それをモノマーとするポリマー、及びそれらの遷移金属錯体 |
| JP3892932B2 (ja) | 1997-03-11 | 2007-03-14 | 高砂香料工業株式会社 | ビニル基を有する光学活性ホスフィン誘導体、それをモノマーとするポリマー、及びそれらの遷移金属錯体 |
| US6121184A (en) | 1997-07-29 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Supported bis(phosphorus) ligands |
-
1999
- 1999-04-14 US US09/291,878 patent/US6229052B1/en not_active Expired - Fee Related
- 1999-05-26 BR BR9911205-1A patent/BR9911205A/pt not_active IP Right Cessation
- 1999-05-26 JP JP2000552070A patent/JP4309057B2/ja not_active Expired - Fee Related
- 1999-05-26 EP EP99925835A patent/EP1082285B1/en not_active Expired - Lifetime
- 1999-05-26 ES ES99925835T patent/ES2224669T3/es not_active Expired - Lifetime
- 1999-05-26 KR KR1020007013379A patent/KR100580420B1/ko not_active Expired - Fee Related
- 1999-05-26 CA CA002330153A patent/CA2330153A1/en not_active Abandoned
- 1999-05-26 WO PCT/US1999/011557 patent/WO1999062855A1/en not_active Ceased
- 1999-05-26 AT AT99925835T patent/ATE271532T1/de not_active IP Right Cessation
- 1999-05-26 ID IDW20002470A patent/ID26775A/id unknown
- 1999-05-26 DE DE69918828T patent/DE69918828T2/de not_active Expired - Lifetime
- 1999-05-28 MY MYPI99002133A patent/MY121451A/en unknown
- 1999-08-27 TW TW088108921A patent/TWI253448B/zh not_active IP Right Cessation
-
2001
- 2001-02-16 US US09/784,909 patent/US6369257B1/en not_active Expired - Fee Related
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