JP2001516640A5 - - Google Patents
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- Publication number
- JP2001516640A5 JP2001516640A5 JP2000511587A JP2000511587A JP2001516640A5 JP 2001516640 A5 JP2001516640 A5 JP 2001516640A5 JP 2000511587 A JP2000511587 A JP 2000511587A JP 2000511587 A JP2000511587 A JP 2000511587A JP 2001516640 A5 JP2001516640 A5 JP 2001516640A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- formula
- aryl
- cyano
- nitro
- 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- Withdrawn
Links
- 125000000217 alkyl group Chemical group 0.000 description 19
- 125000003118 aryl group Chemical group 0.000 description 18
- 125000003545 alkoxy group Chemical group 0.000 description 12
- 229910052736 halogen Inorganic materials 0.000 description 12
- 150000002367 halogens Chemical class 0.000 description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 11
- 125000000753 cycloalkyl group Chemical group 0.000 description 11
- 125000001424 substituent group Chemical group 0.000 description 10
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- -1 cyano, carboxyl Chemical group 0.000 description 7
- 125000001072 heteroaryl group Chemical group 0.000 description 7
- 125000004093 cyano group Chemical group *C#N 0.000 description 6
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical group OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 6
- 125000004104 aryloxy group Chemical group 0.000 description 5
- 125000000000 cycloalkoxy group Chemical group 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 239000003446 ligand Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 238000005669 hydrocyanation reaction Methods 0.000 description 3
- 238000006317 isomerization reaction Methods 0.000 description 3
- UVKXJAUUKPDDNW-NSCUHMNNSA-N (e)-pent-3-enenitrile Chemical compound C\C=C\CC#N UVKXJAUUKPDDNW-NSCUHMNNSA-N 0.000 description 2
- IHXNSHZBFXGOJM-UHFFFAOYSA-N 2-methylbut-2-enenitrile Chemical class CC=C(C)C#N IHXNSHZBFXGOJM-UHFFFAOYSA-N 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- CFEYBLWMNFZOPB-UHFFFAOYSA-N pent-4-enenitrile Chemical compound C=CCCC#N CFEYBLWMNFZOPB-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- WBAXCOMEMKANRN-UHFFFAOYSA-N 2-methylbut-3-enenitrile Chemical compound C=CC(C)C#N WBAXCOMEMKANRN-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- ISBHMJZRKAFTGE-UHFFFAOYSA-N pent-2-enenitrile Chemical compound CCC=CC#N ISBHMJZRKAFTGE-UHFFFAOYSA-N 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19740180.5 | 1997-09-12 | ||
| DE19740180A DE19740180A1 (de) | 1997-09-12 | 1997-09-12 | Katalysator, umfassend wenigstens einen Nickel(0)Komplex auf Basis eines Phosphonitliganden und Verfahren zur Herstellung von Nitrilen |
| PCT/EP1998/005733 WO1999013983A1 (de) | 1997-09-12 | 1998-09-09 | Katalysator, umfassend wenigstens einen nickel(o)komplex auf basis eines phosphonitliganden und verfahren zur herstellung von nitrilen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2001516640A JP2001516640A (ja) | 2001-10-02 |
| JP2001516640A5 true JP2001516640A5 (enExample) | 2006-01-05 |
Family
ID=7842178
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000511587A Withdrawn JP2001516640A (ja) | 1997-09-12 | 1998-09-09 | ホスホナイト配位子を基礎とする少なくとも一種類のニッケル（０）錯体を含有する触媒、及びニトリルの製造方法 |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US6242633B1 (enExample) |
| EP (1) | EP1019190B1 (enExample) |
| JP (1) | JP2001516640A (enExample) |
| KR (1) | KR100555259B1 (enExample) |
| CN (1) | CN1222358C (enExample) |
| AR (1) | AR017076A1 (enExample) |
| AU (1) | AU9538598A (enExample) |
| BR (1) | BR9812207A (enExample) |
| CA (1) | CA2303776A1 (enExample) |
| DE (2) | DE19740180A1 (enExample) |
| ES (1) | ES2234158T3 (enExample) |
| ID (1) | ID24451A (enExample) |
| MY (1) | MY118720A (enExample) |
| TW (1) | TW400249B (enExample) |
| WO (1) | WO1999013983A1 (enExample) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19810794A1 (de) * | 1998-03-12 | 1999-09-16 | Basf Ag | Katalysator, umfassend einen Komplex eines Metalls der VIII. Nebengruppe auf Basis eines Phosphonitliganden und Verfahren zur Hydroformylierung |
| DE19825212A1 (de) * | 1998-06-05 | 1999-12-09 | Basf Ag | Katalysator, umfassend einen Komplex eines Metalls der VIII. Nebengruppe auf Basis eines zweizähnigen Phosphonitliganden und Verfahren zur Herstellung von Nitrilen |
| RU2226228C2 (ru) * | 1999-08-20 | 2004-03-27 | Дю Пон Де Немур Энтернасьональ С.А. | Способ электрохимического получения ni(о) фосфитных и дифосфитных комплексов |
| DE10049265A1 (de) * | 2000-09-28 | 2002-04-11 | Basf Ag | Verfahren zur Trennung von Pentennitril-Isomeren |
| DE10136488A1 (de) * | 2001-07-27 | 2003-02-06 | Basf Ag | Ni(O) enthaltendes Katalysatorsystem |
| DE10150286A1 (de) * | 2001-10-12 | 2003-04-17 | Basf Ag | Phosphinite |
| 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 |
| MY138064A (en) * | 2002-01-24 | 2009-04-30 | Basf Ag | Method for the separation of acids from chemical reaction mixtures by means of ionic fluids |
| TW504991U (en) * | 2002-01-31 | 2002-10-01 | Kuo-Chan Weng | Inner lock device for sliding rail of drawer |
| US6660877B2 (en) * | 2002-03-07 | 2003-12-09 | E. I. Du Pont De Nemours And Company | Phosphonite ligands and their use in hydrocyanation |
| EP1344770A1 (en) * | 2002-03-12 | 2003-09-17 | E.I. du Pont de Nemours and Company | Process for the hydrocyanation of butadiene |
| FR2850966B1 (fr) | 2003-02-10 | 2005-03-18 | Rhodia Polyamide Intermediates | Procede de fabrication de composes dinitriles |
| DE10311122A1 (de) * | 2003-03-12 | 2004-09-23 | Basf Ag | Verfahren zur Hydrocyanierung einer olefinisch ungesättigten Verbindung |
| FR2854891B1 (fr) | 2003-05-12 | 2006-07-07 | Rhodia Polyamide Intermediates | Procede de preparation de dinitriles |
| DE10350999A1 (de) | 2003-10-30 | 2005-06-02 | Basf Ag | Katalysator, umfassend wenigstens einen Nickel(O)Komplex stabilisiert durch einen sterisch anspruchsvollen Chelatphosphinitphosphitliganden, sowie ein Verfahren zur Herstellung von Nitrilen |
| ATE507202T1 (de) * | 2004-01-29 | 2011-05-15 | Basf Se | Verfahren zur herstellung von linearem pentennitril |
| DE102004004721A1 (de) * | 2004-01-29 | 2005-08-18 | Basf Ag | Verfahren zur Trennung von Pentennitril-Isomeren |
| DE102004004718A1 (de) * | 2004-01-29 | 2005-08-18 | Basf Ag | Verfahren zur Hydrocyanierung |
| DE102004004682A1 (de) * | 2004-01-29 | 2005-08-18 | Basf Ag | Verfahren zur Herstellung von Adipodinitril durch Hydrocyanierung von 1,3-Butadien |
| DE102004004697A1 (de) * | 2004-01-29 | 2005-08-18 | Basf Ag | Verfahren zur Herstellung von Pentennitrilen aus n-Butan |
| US7973174B2 (en) | 2005-10-18 | 2011-07-05 | Invista North America S.A.R.L. | Process of making 3-aminopentanenitrile |
| MX2008011640A (es) | 2006-03-17 | 2008-09-22 | Invista Tech Sarl | Metodo para la purificacion de triorganofosfitos por tratamiento con un aditivo basico. |
| US7709674B2 (en) * | 2006-07-14 | 2010-05-04 | Invista North America S.A R.L | Hydrocyanation process with reduced yield losses |
| US7919646B2 (en) | 2006-07-14 | 2011-04-05 | Invista North America S.A R.L. | Hydrocyanation of 2-pentenenitrile |
| US7880028B2 (en) | 2006-07-14 | 2011-02-01 | Invista North America S.A R.L. | Process for making 3-pentenenitrile by hydrocyanation of butadiene |
| WO2009075692A2 (en) | 2007-05-14 | 2009-06-18 | Invista Technologies S.A.R.L. | High efficiency reactor and process |
| WO2008157218A1 (en) | 2007-06-13 | 2008-12-24 | Invista Technologies S.A.R.L. | Process for improving adiponitrile quality |
| WO2009091790A1 (en) * | 2008-01-15 | 2009-07-23 | Invista Technologies S.A.R.L. | Hydrocyanation of pentenenitriles |
| CN101910119B (zh) | 2008-01-15 | 2013-05-29 | 因温斯特技术公司 | 用于制备和精制3-戊烯腈，和用于精制2-甲基-3-丁烯腈的方法 |
| WO2009117498A2 (en) * | 2008-03-19 | 2009-09-24 | Invista Technologies S.A R.L. | Methods of making cyclododecatriene and methods of making laurolactone |
| WO2010045131A1 (en) | 2008-10-14 | 2010-04-22 | Invista Technologies S.A.R.L. | Process for making 2-secondary-alkyl-4,5-di-(normal-alkyl)phenols |
| FR2946649B1 (fr) * | 2009-06-16 | 2012-04-13 | Rhodia Operations | Procede de fabrication de composes nitriles a partir de composes a insaturation ethylenique |
| EP2462103A4 (en) | 2009-08-07 | 2014-01-08 | Invista Tech Sarl | HYDROGENATION AND STAFFING FOR THE FORMATION OF DIES |
| WO2011075494A1 (en) | 2009-12-18 | 2011-06-23 | Invista Technologies S.A.R.L. | Nickel metal compositions and nickel complexes derived from basic nickel carbonates |
| ES2448957T3 (es) | 2010-07-07 | 2014-03-17 | Invista Technologies S.À.R.L. | Procedimiento de producción de nitrilos |
| EP2614071B1 (en) * | 2010-09-07 | 2015-12-02 | Invista Technologies S.a r.l. | Preparing a nickel phosphorus ligand complex |
| CN104379590B (zh) * | 2012-06-01 | 2017-10-27 | 英威达纺织（英国）有限公司 | 稳定氢氰化催化剂的方法 |
| US9406974B2 (en) * | 2013-04-25 | 2016-08-02 | Samsung Sdi Co., Ltd. | Additive for electrolyte of lithium battery, organic electrolytic solution comprising the same, and lithium battery using the organic electrolytic solution |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2161750A1 (de) * | 1971-12-13 | 1973-06-14 | Henkel & Cie Gmbh | Verfahren zur herstellung von tertiaeren aminen |
| US3766237A (en) | 1972-01-25 | 1973-10-16 | Du Pont | Hydrocyanation of olefins |
| US5175335A (en) | 1991-11-12 | 1992-12-29 | E. I. Du Pont De Nemours And Company | Enantioselective hydrocyanation of aromatic vinyl compounds |
| DE4321194A1 (de) * | 1993-06-25 | 1995-01-05 | Basf Ag | Phosphorhaltige Calixarene |
| US5597569A (en) * | 1993-10-25 | 1997-01-28 | Bristol-Myers Squibb Company | Bryodin 2 a ribosome-inactivating protein isolated from the plant Bryonia dioica |
| 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 |
| DE69519020T2 (de) | 1994-04-14 | 2001-05-17 | E.I. Du Pont De Nemours And Co., Wilmington | Nickel und phosphinebidentat enthaltende katalysatorzusammen- setzungen zur hydrocyanierung von monoolefinen |
| US5543536A (en) * | 1994-04-26 | 1996-08-06 | E. I. Du Pont De Nemours And Company | Monodentate phosphite and nickel catalyst composition for monoolefin hydrocyanation |
| US5600032A (en) | 1994-06-29 | 1997-02-04 | Mitsubishi Chemical Corporation | Method for producing an unsaturated alcohol |
| TW315370B (enExample) | 1994-10-07 | 1997-09-11 | Du Pont | |
| IN187044B (enExample) * | 1995-01-27 | 2002-01-05 | Du Pont | |
| US5523453A (en) | 1995-03-22 | 1996-06-04 | E. I. Du Pont De Nemours And Company | Process for hydrocyanation |
-
1997
- 1997-09-12 DE DE19740180A patent/DE19740180A1/de not_active Withdrawn
-
1998
- 1998-09-08 AR ARP980104469A patent/AR017076A1/es unknown
- 1998-09-09 ES ES98948941T patent/ES2234158T3/es not_active Expired - Lifetime
- 1998-09-09 ID IDW20000485A patent/ID24451A/id unknown
- 1998-09-09 AU AU95385/98A patent/AU9538598A/en not_active Abandoned
- 1998-09-09 BR BR9812207-0A patent/BR9812207A/pt not_active Application Discontinuation
- 1998-09-09 CN CNB988090449A patent/CN1222358C/zh not_active Expired - Fee Related
- 1998-09-09 WO PCT/EP1998/005733 patent/WO1999013983A1/de not_active Ceased
- 1998-09-09 CA CA002303776A patent/CA2303776A1/en not_active Abandoned
- 1998-09-09 US US09/508,051 patent/US6242633B1/en not_active Expired - Fee Related
- 1998-09-09 TW TW087114963A patent/TW400249B/zh not_active IP Right Cessation
- 1998-09-09 KR KR1020007002600A patent/KR100555259B1/ko not_active Expired - Fee Related
- 1998-09-09 EP EP98948941A patent/EP1019190B1/de not_active Expired - Lifetime
- 1998-09-09 DE DE59812339T patent/DE59812339D1/de not_active Expired - Fee Related
- 1998-09-09 JP JP2000511587A patent/JP2001516640A/ja not_active Withdrawn
- 1998-09-10 MY MYPI98004153A patent/MY118720A/en unknown
-
2001
- 2001-02-14 US US09/782,762 patent/US6355833B2/en not_active Expired - Fee Related
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