CN1041301C - 烯烃的羰基化 - Google Patents

烯烃的羰基化 Download PDF

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Publication number
CN1041301C
CN1041301C CN92100234A CN92100234A CN1041301C CN 1041301 C CN1041301 C CN 1041301C CN 92100234 A CN92100234 A CN 92100234A CN 92100234 A CN92100234 A CN 92100234A CN 1041301 C CN1041301 C CN 1041301C
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CN
China
Prior art keywords
acid
source
group
reaction
ethylenically unsaturated
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Expired - Lifetime
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CN92100234A
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English (en)
Chinese (zh)
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CN1063277A (zh
Inventor
E·德伦特
E·克拉特维克
D·H·L·帕罗
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LUXIT INTERNATIONAL UK Ltd
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Shell Internationale Research Maatschappij BV
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Priority claimed from GB919100801A external-priority patent/GB9100801D0/en
Priority claimed from GB919105211A external-priority patent/GB9105211D0/en
Priority claimed from GB919118631A external-priority patent/GB9118631D0/en
Application filed by Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of CN1063277A publication Critical patent/CN1063277A/zh
Application granted granted Critical
Publication of CN1041301C publication Critical patent/CN1041301C/zh
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2419—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member
    • B01J31/2428—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member with more than one complexing phosphine-P atom
    • B01J31/2433—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising P as ring member with more than one complexing phosphine-P atom comprising aliphatic or saturated rings
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201—Oxygen-containing compounds
    • B01J31/0202—Alcohols or phenols
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201—Oxygen-containing compounds
    • B01J31/0205—Oxygen-containing compounds comprising carbonyl groups or oxygen-containing derivatives, e.g. acetals, ketals, cyclic peroxides
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0215—Sulfur-containing compounds
    • B01J31/0217—Mercaptans or thiols
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235—Nitrogen containing compounds
    • B01J31/0237—Amines
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235—Nitrogen containing compounds
    • B01J31/0245—Nitrogen containing compounds being derivatives of carboxylic or carbonic acids
    • B01J31/0247—Imides, amides or imidates (R-C=NR(OR))
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
    • 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
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • 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
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2409—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom
    • B01J31/2414—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom comprising aliphatic or saturated rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B41/00—Formation or introduction of functional groups containing oxygen
    • C07B41/06—Formation or introduction of functional groups containing oxygen of carbonyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00—Preparation of carboxylic acid amides
    • C07C231/10—Preparation of carboxylic acid amides from compounds not provided for in groups C07C231/02 - C07C231/08
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/17—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and doubly-bound oxygen atoms bound to the same acyclic carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C07C51/14—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
    • C07C67/38—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates by addition to an unsaturated carbon-to-carbon bond
    • 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
    • B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • 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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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
CN92100234A 1991-01-15 1992-01-13 烯烃的羰基化 Expired - Lifetime CN1041301C (zh)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
GB919100801A GB9100801D0 (en) 1991-01-15 1991-01-15 Carbonylation of olefins
GB9100801.1 1991-01-15
GB9105211.8 1991-03-12
GB919105211A GB9105211D0 (en) 1991-03-12 1991-03-12 Process for the preparation of alkanedioic acid derivatives
GB919118631A GB9118631D0 (en) 1991-08-30 1991-08-30 Carbonylation of olefins
GB9118631.2 1991-08-30

Publications (2)

Publication Number Publication Date
CN1063277A CN1063277A (zh) 1992-08-05
CN1041301C true CN1041301C (zh) 1998-12-23

Family

ID=27265453

Family Applications (1)

Application Number Title Priority Date Filing Date
CN92100234A Expired - Lifetime CN1041301C (zh) 1991-01-15 1992-01-13 烯烃的羰基化

Country Status (8)

Country Link
EP (1) EP0495547B1 (OSRAM)
JP (1) JP3270098B2 (OSRAM)
CN (1) CN1041301C (OSRAM)
CA (1) CA2059233C (OSRAM)
DE (1) DE69210054T2 (OSRAM)
ES (1) ES2088082T3 (OSRAM)
IN (1) IN185157B (OSRAM)
SG (1) SG45352A1 (OSRAM)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5380819A (en) * 1992-03-27 1995-01-10 Kureha Kagaku Kogyo K.K. Resin composition including poly(arylene thioether) and polyamide
SG49630A1 (en) * 1992-04-08 1998-06-15 Shell Int Research Carbonylation process using palladium phosphine catalyst
US5436356A (en) * 1993-02-09 1995-07-25 Shell Oil Company Carbonylation process
US5290743A (en) * 1993-03-22 1994-03-01 Arco Chemical Technology L.P. Process for regenerating a deactivated rhodium hydroformylation catalyst system
US5488096A (en) * 1993-06-29 1996-01-30 Shell Oil Company Copolymers of carbon monoxide and an olefinically unsaturated compound and process for the preparation thereof
EP0632084B1 (en) * 1993-06-29 1999-09-01 Shell Internationale Researchmaatschappij B.V. Copolymers of carbon monoxide and an olefinically unsaturated compound and process for the preparation thereof
DE69409651T2 (de) * 1993-07-19 1998-08-06 Shell Int Research Verfahren zur carbonylierung von acetylenisch ungesättigten verbindungen
WO1995005354A1 (en) * 1993-08-19 1995-02-23 Shell Internationale Research Maatschappij B.V. Hydroformylation process
US5488174A (en) * 1993-08-19 1996-01-30 Shell Oil Company Hydroformylation process
GB9325377D0 (en) * 1993-12-10 1994-02-16 Ici Plc Process for the carbonylation of an acetylenically unsaturated compound
BE1008018A3 (nl) * 1994-01-06 1995-12-12 Dsm Nv Werkwijze voor de bereiding van een ester.
FR2721926B1 (fr) * 1994-06-29 1996-08-23 Inst Nat Ploytechnique De Toul Procede de preparation stereoselective de composes cycliques terpeniques carbonyles par cyclocarbonylation catalytique, et applications de ces composes comme desinfectants ou produits odoriferants
DE4424710A1 (de) * 1994-07-13 1996-01-18 Basf Ag Verfahren zur Carbonylierung von Olefinen
US5495041A (en) * 1995-02-22 1996-02-27 Dsm N.W. Process for the preparation of a pentenoate ester
ZA965990B (en) * 1995-07-17 1997-02-24 Shell Int Research Process for the continuous carbonylation of olefins.
DE19530992A1 (de) * 1995-08-23 1997-02-27 Basf Ag Verfahren zur Herstellung von Carbonsäuren durch Carbonylierung von Olefinen
US5618983A (en) * 1995-08-25 1997-04-08 E. I. Du Pont De Nemours And Company Hydroformylation process
EP0846097B1 (en) * 1995-08-25 2000-11-02 E.I. Du Pont De Nemours And Company Hydroformylation process
US5670700A (en) * 1995-08-25 1997-09-23 E. I. Du Pont De Nemours And Company Hydroformylation process
US5631400A (en) * 1995-12-19 1997-05-20 Shell Oil Company Carbonylation process
GB9705699D0 (en) † 1997-03-19 1997-05-07 Ici Plc Process for the carbonylation of ethylene
US6156934A (en) * 1997-03-26 2000-12-05 Shell Oil Company Diphosphines
US6127582A (en) * 1997-08-27 2000-10-03 Shell Oil Company Hydroformylation process
DE69802360T2 (de) * 1997-09-18 2002-10-17 Shell Internationale Research Maatschappij B.V., Den Haag/S'gravenhage Hydroformylierungsverfahren
US5952530A (en) * 1998-02-02 1999-09-14 Union Carbide Chemicals & Plastics Technology Corporation Separation processes
US6156936A (en) * 1998-03-16 2000-12-05 Shell Oil Company Hydroformylation of olefin feeds containing dienes
DE19840253A1 (de) * 1998-09-03 2000-03-09 Basf Ag Verfahren zur Herstellung von Cyanvaleriansäure oder -estern
MY127358A (en) 2000-03-14 2006-11-30 Shell Int Research Process for the carbonylation of ethylenically unsaturated compounds
US6743911B2 (en) 2000-03-14 2004-06-01 Shell Oil Company Process for the carbonylation of pentenenitrile
MY127093A (en) 2000-05-17 2006-11-30 Lucite Int Uk Ltd Bidentate ligands useful in catalyst systems
DE10048874A1 (de) 2000-09-29 2002-04-11 Basf Ag Katalysatorsystem und Verfahren zur Carbonylierung
CN1535180A (zh) * 2001-01-31 2004-10-06 国际壳牌研究有限公司 烯属不饱和化合物的羰基化方法,用于此方法的双齿二膦组合物和此双齿二膦组合物的制备方法
DE10228293A1 (de) 2001-07-28 2003-02-13 Basf Ag Verfahren zur Herstellung von Dialkylketonen
DE10148712A1 (de) 2001-10-02 2003-04-17 Basf Ag Diphosphin
US20030105348A1 (en) 2001-11-19 2003-06-05 Bunel Emilio E. Process for making 5-cyanovaleric acid, adipic acid or dimethyl adipate
US7084089B2 (en) 2002-07-31 2006-08-01 Shell Oil Company Process for the carbonylation of ethylenically unsaturated compounds, bidentate diphosphine composition used in this process and a process for preparation of this bidentate diphosphine composition
US6806391B2 (en) 2002-07-31 2004-10-19 Shell Oil Company Process for the carbonylation of ethylenically unsaturated compounds and bidentate diphosphine composition used in this process
TWI301481B (en) 2002-08-10 2008-10-01 Lucite Int Uk Ltd A catalyst system
AU2003299066A1 (en) 2002-09-26 2004-04-19 Shell Internationale Research Maatschappij B.V. Process for the hydroformylation of an ethylenically unsaturated compound using a bidentate diphosphine composition with a bridging group comprising sp2 hybridized carbon atoms bound to the phosphorous atoms
WO2005003070A1 (en) 2003-07-03 2005-01-13 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
GB0426894D0 (en) * 2004-12-08 2005-01-12 Stylacats Ltd Process
GB0516556D0 (en) 2005-08-12 2005-09-21 Lucite Int Uk Ltd Improved catalyst system
CA2626107C (en) 2005-11-17 2016-06-21 Lucite International Uk Limited Carbonylation of ethylenically unsaturated compounds
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
BRPI0719344B1 (pt) 2006-12-02 2017-05-02 Lucite Int Uk Ltd ligando bidentado, processo para a carbonilação de compostos etilenicamente insaturados, e, sistema de catalisador
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
GB0921876D0 (en) 2009-12-15 2010-01-27 Lucite Int Uk Ltd Improved carbonylation process
GB0921875D0 (en) 2009-12-15 2010-01-27 Lucite Int Uk Ltd A continuous process for the carbonylation of ethylene
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
GB201122054D0 (en) 2011-12-21 2012-02-01 Lucite Int Uk Ltd A continuous process for the carbonylation of ethylene
CN106795083A (zh) 2014-10-17 2017-05-31 陶氏环球技术有限责任公司 用于羧酸的气相制造的催化剂
CN107497489B (zh) * 2016-06-14 2020-06-09 中国石油化工股份有限公司 乙烯合成丙酸甲酯用催化剂组合物及其合成方法
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
CN115819234B (zh) * 2021-12-21 2025-04-29 浙江新和成股份有限公司 一种烯烃羰基化反应的方法

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6241A (ja) * 1985-06-21 1987-01-06 ロ−ヌ−プ−ラン・スペシアリテ・シミ−ク 芳香族アルデヒドの製造方法
JPS6272643A (ja) * 1985-09-27 1987-04-03 シエル・インタ−ナシヨネイル・リサ−チ・マ−チヤツピイ・ベ−・ウイ 不飽和ケトンの製造法
GB2185740A (en) * 1986-01-27 1987-07-29 Shell Int Research Process for the preparation of ketones
CN88101206A (zh) * 1987-03-11 1988-09-28 国际壳牌研究有限公司 在钯催化剂下烯属不饱和化合物羰基化的方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3168553A (en) * 1961-08-25 1965-02-02 Shell Oil Co Reactions of olefins with carbon monoxide
GB8531624D0 (en) * 1985-12-23 1986-02-05 Shell Int Research Carbonylation of ethylenically unsaturated compounds
IL90881A0 (en) * 1989-07-05 1990-02-09 Yeda Res & Dev Production of aldehydes

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6241A (ja) * 1985-06-21 1987-01-06 ロ−ヌ−プ−ラン・スペシアリテ・シミ−ク 芳香族アルデヒドの製造方法
JPS6272643A (ja) * 1985-09-27 1987-04-03 シエル・インタ−ナシヨネイル・リサ−チ・マ−チヤツピイ・ベ−・ウイ 不飽和ケトンの製造法
GB2185740A (en) * 1986-01-27 1987-07-29 Shell Int Research Process for the preparation of ketones
CN88101206A (zh) * 1987-03-11 1988-09-28 国际壳牌研究有限公司 在钯催化剂下烯属不饱和化合物羰基化的方法

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JP3270098B2 (ja) 2002-04-02
CA2059233A1 (en) 1992-07-16
ES2088082T3 (es) 1996-08-01
DE69210054D1 (de) 1996-05-30
EP0495547A2 (en) 1992-07-22
EP0495547B1 (en) 1996-04-24
SG45352A1 (en) 1998-01-16
JPH04334340A (ja) 1992-11-20
CN1063277A (zh) 1992-08-05
IN185157B (OSRAM) 2000-11-25
DE69210054T2 (de) 1996-12-12
CA2059233C (en) 2003-02-04
EP0495547A3 (en) 1993-02-03

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