AR018438A1 - Catalizador que comprende un complejo de un metal del subgrupo viii; ligando fosfonito comprendido en el mismo; procedimiento para la preparacion de mezclas de c5-mononitrilos monoolefinicos con enlace c=c y c triple ligadura n no conjugado por hidrocianuracion catalitica de butadieno o una mezcla d - Google Patents
Catalizador que comprende un complejo de un metal del subgrupo viii; ligando fosfonito comprendido en el mismo; procedimiento para la preparacion de mezclas de c5-mononitrilos monoolefinicos con enlace c=c y c triple ligadura n no conjugado por hidrocianuracion catalitica de butadieno o una mezcla dInfo
- Publication number
- AR018438A1 AR018438A1 ARP990102601A ARP990102601A AR018438A1 AR 018438 A1 AR018438 A1 AR 018438A1 AR P990102601 A ARP990102601 A AR P990102601A AR P990102601 A ARP990102601 A AR P990102601A AR 018438 A1 AR018438 A1 AR 018438A1
- Authority
- AR
- Argentina
- Prior art keywords
- aryl
- preparation
- alkyl
- cycloalkyl
- catalyst
- Prior art date
Links
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 title abstract 5
- 239000003054 catalyst Substances 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 4
- BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- -1 c icloalkyl Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 150000004985 diamines Chemical class 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical class NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 1
- 230000036571 hydration Effects 0.000 abstract 1
- 238000006703 hydration reaction Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/48—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof
- C07F9/4866—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof the ester moiety containing a substituent or structure which is considered as characteristic
- C07F9/4875—Esters with hydroxy aryl compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
- B01J31/1865—Phosphonites (RP(OR)2), their isomeric phosphinates (R2(RO)P=O) and RO-substitution derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/08—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds
- C07C253/10—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds to compounds containing carbon-to-carbon double bonds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/323—Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
- B01J2231/52—Isomerisation reactions
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0261—Complexes comprising ligands with non-tetrahedral chirality
- B01J2531/0266—Axially chiral or atropisomeric ligands, e.g. bulky biaryls such as donor-substituted binaphthalenes, e.g. "BINAP" or "BINOL"
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/821—Ruthenium
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/822—Rhodium
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/824—Palladium
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/845—Cobalt
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/847—Nickel
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Toxicology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Para la preparacion en escala industrial de las poliamidas existe un gran requerimiento en todo el mundo de alfa,omega-alquilendiaminas, las cuales seutilizan como un importante producto de partida. las alfa,omega-alquilendiaminas, como por ej., lah exametilendiamina, se obtienen casi exclusivamente porhidratacion de los dinitrilos correspondientes. Casi todos los caminos para la preparacion de hexametilendiaminas en escala industrial son por lo tantosustancialmente variantes de lapreparacion d el adiponitrilo, del cual se producen anualmente en todo el mundo aproximadamente 1,0 millones de toneladas. uncatalizador que presenta buena selectividad y buena actividad catalítica en la hidrocianuracion de 1,3-butadieno y demezclas de hidrocarbu ros que contienen1,3-butadieno y para la preparacion de adipodinitrilo, que comprende un complejo de un metal del subgrupo VIII con un ligando fosfonito bidentado de laformula general (I) en donde: A representa un puentealquileno C2-7, que puede pre sentar 1, 2 o 3 enlaces dobles y/o 1, 2 o 3 sustituyentes, seleccionadosentre alquilo, cicloalquilo y arilo, en donde el sustituyente arilo puede tener adicionalmente 1, 2 o 3 sustituyentes seleccionados entre alquilo,alcoxi,halogeno, trifluorometil o, nitro, alcoxicarbonilo o ciano, y/o el puente alquileno C2-7 puede estar interrumpido por 1,2 o 3 heteroátomos no vecinos,eventualmente sustituidos, y/o el puente alquileno C2-7 puede estar condensado 1, 2 o 3veces con arilo y/o hetarilo, en dond e los grupos arilo y hetarilocondensados pueden tener 1, 2 o 3 sustituyentes seleccionados entre alquilo, cicloalquilo, arilo, alcoxi, cicloalcoxi, ariloxi, acilo, halogeno,trifluorometilo, nitro, ciano,carboxilo, alcoxicarbonilo o NE1E2, en donde E 1 y E2 pueden ser iguales o diferentes y representan alquilo, cicloalquilo oarilo; R1 y R1 independientemente uno de otro representan alquilo, cicloalquilo, arilo o hetearilo, que pueden tener 1, 2 o 3sustituyentes seleccionadosentre alquilo, cicloa lquilo o arilo; R2 y R2 independientemente uno de otro representan alquilo, cicloalquilo, arilo o hetarilo, en donde los grupos arilo y
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19825212A DE19825212A1 (de) | 1998-06-05 | 1998-06-05 | Katalysator, umfassend einen Komplex eines Metalls der VIII. Nebengruppe auf Basis eines zweizähnigen Phosphonitliganden und Verfahren zur Herstellung von Nitrilen |
Publications (1)
Publication Number | Publication Date |
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AR018438A1 true AR018438A1 (es) | 2001-11-14 |
Family
ID=7870052
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP990102601A AR018438A1 (es) | 1998-06-05 | 1999-06-02 | Catalizador que comprende un complejo de un metal del subgrupo viii; ligando fosfonito comprendido en el mismo; procedimiento para la preparacion de mezclas de c5-mononitrilos monoolefinicos con enlace c=c y c triple ligadura n no conjugado por hidrocianuracion catalitica de butadieno o una mezcla d |
Country Status (16)
Country | Link |
---|---|
US (1) | US6521778B1 (es) |
EP (1) | EP1091804B1 (es) |
JP (1) | JP4480058B2 (es) |
KR (1) | KR100576667B1 (es) |
CN (1) | CN1159106C (es) |
AR (1) | AR018438A1 (es) |
BR (1) | BR9910956B1 (es) |
CA (1) | CA2334151C (es) |
DE (2) | DE19825212A1 (es) |
ES (1) | ES2173750T3 (es) |
ID (1) | ID27071A (es) |
MY (1) | MY120574A (es) |
RU (1) | RU2223146C2 (es) |
TR (1) | TR200003625T2 (es) |
TW (1) | TW519496B (es) |
WO (1) | WO1999064155A1 (es) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
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DE10046026A1 (de) * | 2000-09-18 | 2002-03-28 | Basf Ag | Verfahren zur Hydroformylierung, Xanthen-verbrückte Liganden und Katalysator, umfassend einen Komplex dieser Liganden |
DE10136488A1 (de) * | 2001-07-27 | 2003-02-06 | Basf Ag | Ni(O) enthaltendes Katalysatorsystem |
AR036636A1 (es) * | 2001-10-12 | 2004-09-22 | Basf Ag | Fosfonita i, su uso como ligando en complejos de metal de transicion, dichos complejos, procedimiento para la obtencion de estos ultimos, uso de complejos de metal transitorio como catalizador y procedimientos para la adicion de acido cianhidrico a un doble enlace olefinico y para la isomerizacion d |
DE10150285A1 (de) * | 2001-10-12 | 2003-04-17 | Basf Ag | Phosphonite |
DE10150286A1 (de) * | 2001-10-12 | 2003-04-17 | Basf Ag | Phosphinite |
DE10156292A1 (de) * | 2001-11-19 | 2003-05-28 | Basf Ag | Verfahren zur Herstellung von Organodiphosphoniten |
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 |
US6660877B2 (en) | 2002-03-07 | 2003-12-09 | E. I. Du Pont De Nemours And Company | Phosphonite ligands and their use in hydrocyanation |
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 |
FR2850966B1 (fr) | 2003-02-10 | 2005-03-18 | Rhodia Polyamide Intermediates | Procede de fabrication de composes dinitriles |
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 |
DE102004004718A1 (de) | 2004-01-29 | 2005-08-18 | Basf Ag | Verfahren zur Hydrocyanierung |
US7973174B2 (en) | 2005-10-18 | 2011-07-05 | Invista North America S.A.R.L. | Process of making 3-aminopentanenitrile |
CZ2008547A3 (cs) | 2006-03-17 | 2009-06-10 | Invista Technologies S. A. R. L. | Zpusob purifikace triorganofosfitu ošetrením bazickým aditivem |
US7880028B2 (en) | 2006-07-14 | 2011-02-01 | Invista North America S.A R.L. | Process for making 3-pentenenitrile by hydrocyanation of butadiene |
US7919646B2 (en) | 2006-07-14 | 2011-04-05 | Invista North America S.A R.L. | Hydrocyanation of 2-pentenenitrile |
US7709674B2 (en) * | 2006-07-14 | 2010-05-04 | Invista North America S.A R.L | Hydrocyanation process with reduced yield losses |
WO2009075692A2 (en) | 2007-05-14 | 2009-06-18 | Invista Technologies S.A.R.L. | High efficiency reactor and process |
CN101952004B (zh) | 2007-06-13 | 2015-08-12 | 因温斯特技术公司 | 改善己二腈质量的方法 |
EP2229353B1 (en) | 2008-01-15 | 2018-01-03 | INVISTA Textiles (U.K.) Limited | 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 |
FR2926816B1 (fr) | 2008-01-25 | 2010-05-14 | Rhodia Operations | Procede de fabrication de composes comprenant des fonctions nitriles |
EP2407444A3 (en) * | 2008-03-19 | 2012-12-05 | Invista Technologies S.à.r.l. | Process for the preparation of dodecanedioic acid |
FR2932477B1 (fr) | 2008-06-17 | 2013-01-18 | Rhodia Operations | Procede de fabrication de composes nitriles a partir de composes a insaturation ethylenique |
KR101610423B1 (ko) | 2008-10-14 | 2016-04-08 | 인비스타 테크놀러지스 에스.에이 알.엘. | 2-sec-알킬-4,5-디-(n-알킬)페놀의 제조 방법 |
FR2937321B1 (fr) | 2008-10-21 | 2010-10-22 | Rhodia Operations | Procede de fabrication de composes comprenant des fonctions nitriles |
FR2941455B1 (fr) | 2009-01-29 | 2011-02-11 | Rhodia Operations | Procede de fabrication de composes comprenant des fonctions nitriles |
WO2011017543A1 (en) | 2009-08-07 | 2011-02-10 | Invista Technologies S.A. R.L. | Hydrogenation and esterification to form diesters |
CN103080074B (zh) | 2010-07-07 | 2015-08-12 | 因温斯特技术公司 | 用于制备腈的方法 |
WO2012033556A1 (en) | 2010-09-07 | 2012-03-15 | Invista Technologies S.A R.L. | Preparing a nickel phosphorus ligand complex |
CN102513157B (zh) * | 2011-12-23 | 2013-06-05 | 渤海大学 | 一种基于双吡啶双酰胺有机配体和Keggin型多酸的铜配合物及其合成方法和应用 |
CN104028305B (zh) * | 2014-06-19 | 2016-02-10 | 渤海大学 | 基于丁基吡唑铜配合物修饰的Keggin型晶态材料、制备方法及其在光催化材料方面的应用 |
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US3766237A (en) | 1972-01-25 | 1973-10-16 | Du Pont | Hydrocyanation of olefins |
US4692426A (en) | 1984-06-21 | 1987-09-08 | Sun Refining And Marketing Company | Phosphite-promoted ruthenium-cobalt catalysts for the dealkoxyhydroxymethylation of acetals to form glycol ethers |
US4652542A (en) | 1984-06-21 | 1987-03-24 | Sun Refining And Marketing Company | Ruthenium-cobalt carbonyl catalysts for the dealkoxyhydroxymethylation of acetals to form glycol ethers |
JPH01102039A (ja) * | 1987-10-20 | 1989-04-19 | Sun Refining & Marketing Co | グリコールエーテル生成の為のアセタールのデアルコキシヒドロキシメチル化用ホスホナイト及びホスフィナイト促進ルテニウムーコバルト触媒 |
US5360938A (en) * | 1991-08-21 | 1994-11-01 | Union Carbide Chemicals & Plastics Technology Corporation | Asymmetric syntheses |
KR100263138B1 (ko) | 1993-11-23 | 2000-08-01 | 이.아이,듀우판드네모아앤드캄파니 | 모노올레핀의 하이드로시안화 방법 및 이를 위한 촉매 조성물 |
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 |
US5600032A (en) * | 1994-06-29 | 1997-02-04 | Mitsubishi Chemical Corporation | Method for producing an unsaturated alcohol |
TW315370B (es) | 1994-10-07 | 1997-09-11 | Du Pont | |
US5449807A (en) | 1994-11-18 | 1995-09-12 | E. I. Du Pont De Nemours And Company | Catalyzed vapor phase hydrocyanation of diolefinic compounds |
US5440067A (en) | 1994-11-18 | 1995-08-08 | E. I. Dupont De Nemours And Company | Catalyzed gas phase isomerization of nonconjugated 2-alkyl-3-monoalkenenitriles |
IN187044B (es) | 1995-01-27 | 2002-01-05 | Du Pont | |
US5821378A (en) | 1995-01-27 | 1998-10-13 | E. I. Du Pont De Nemours And Company | Hydrocyanation of diolefins and isomerization of nonconjugated 2-alkyl-3-monoalkenenitriles |
US5523453A (en) | 1995-03-22 | 1996-06-04 | E. I. Du Pont De Nemours And Company | Process for hydrocyanation |
WO1996033969A1 (fr) * | 1995-04-26 | 1996-10-31 | Rhone-Poulenc Chimie | Procede d'hydrocyanation de nitriles insatures en dinitriles |
US5693843A (en) | 1995-12-22 | 1997-12-02 | E. I. Du Pont De Nemours And Company | Process for hydrocyanation of diolefins and isomerization of nonconjugated 2 alkyl-3-monoalkenenitriles |
IN191158B (es) * | 1996-04-02 | 2003-10-11 | Du Pont | |
AU6518398A (en) * | 1997-03-27 | 1998-10-22 | Mitsubishi Chemical Corporation | Process for producing aldehydes |
DE19740180A1 (de) * | 1997-09-12 | 1999-03-18 | Basf Ag | Katalysator, umfassend wenigstens einen Nickel(0)Komplex auf Basis eines Phosphonitliganden und Verfahren zur Herstellung von Nitrilen |
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 |
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1998
- 1998-06-05 DE DE19825212A patent/DE19825212A1/de not_active Withdrawn
-
1999
- 1999-05-26 MY MYPI99002080A patent/MY120574A/en unknown
- 1999-06-02 AR ARP990102601A patent/AR018438A1/es active IP Right Grant
- 1999-06-03 TW TW088109210A patent/TW519496B/zh not_active IP Right Cessation
- 1999-06-04 CA CA002334151A patent/CA2334151C/en not_active Expired - Fee Related
- 1999-06-04 RU RU2001101148/04A patent/RU2223146C2/ru not_active IP Right Cessation
- 1999-06-04 WO PCT/EP1999/003888 patent/WO1999064155A1/de active IP Right Grant
- 1999-06-04 EP EP99927883A patent/EP1091804B1/de not_active Expired - Lifetime
- 1999-06-04 BR BRPI9910956-5A patent/BR9910956B1/pt not_active IP Right Cessation
- 1999-06-04 TR TR2000/03625T patent/TR200003625T2/xx unknown
- 1999-06-04 KR KR1020007013718A patent/KR100576667B1/ko not_active IP Right Cessation
- 1999-06-04 DE DE59900903T patent/DE59900903D1/de not_active Expired - Lifetime
- 1999-06-04 CN CNB998070491A patent/CN1159106C/zh not_active Expired - Fee Related
- 1999-06-04 ES ES99927883T patent/ES2173750T3/es not_active Expired - Lifetime
- 1999-06-04 US US09/701,601 patent/US6521778B1/en not_active Expired - Lifetime
- 1999-06-04 ID IDW20002541A patent/ID27071A/id unknown
- 1999-06-04 JP JP2000553209A patent/JP4480058B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP2002517473A (ja) | 2002-06-18 |
MY120574A (en) | 2005-11-30 |
ID27071A (id) | 2001-02-22 |
US6521778B1 (en) | 2003-02-18 |
WO1999064155A1 (de) | 1999-12-16 |
EP1091804A1 (de) | 2001-04-18 |
CA2334151C (en) | 2007-10-23 |
KR20010052561A (ko) | 2001-06-25 |
BR9910956A (pt) | 2001-03-13 |
DE59900903D1 (de) | 2002-04-04 |
EP1091804B1 (de) | 2002-02-27 |
TR200003625T2 (tr) | 2001-04-20 |
RU2223146C2 (ru) | 2004-02-10 |
CA2334151A1 (en) | 1999-12-16 |
ES2173750T3 (es) | 2002-10-16 |
JP4480058B2 (ja) | 2010-06-16 |
DE19825212A1 (de) | 1999-12-09 |
CN1159106C (zh) | 2004-07-28 |
BR9910956B1 (pt) | 2010-11-16 |
KR100576667B1 (ko) | 2006-05-08 |
CN1304334A (zh) | 2001-07-18 |
TW519496B (en) | 2003-02-01 |
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