SG11201609591PA - Process for preparing an unsaturated carboxylic acid salt - Google Patents

Process for preparing an unsaturated carboxylic acid salt

Info

Publication number
SG11201609591PA
SG11201609591PA SG11201609591PA SG11201609591PA SG11201609591PA SG 11201609591P A SG11201609591P A SG 11201609591PA SG 11201609591P A SG11201609591P A SG 11201609591PA SG 11201609591P A SG11201609591P A SG 11201609591PA SG 11201609591P A SG11201609591P A SG 11201609591PA
Authority
SG
Singapore
Prior art keywords
preparing
carboxylic acid
acid salt
unsaturated carboxylic
unsaturated
Prior art date
Application number
SG11201609591PA
Inventor
Michael Limbach
Ivana Jevtovikj
Subiela Nuria Huguet
Alvaro Gordillo
Sabine Chantal Eileen Stieber
Ronald Lindner
Roig Miriam Bru
Michael Lejkowski
Takeharu Kageyama
Stephan A Schunk
Original Assignee
Basf Se
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=50731956&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201609591P(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Basf Se filed Critical Basf Se
Publication of SG11201609591PA publication Critical patent/SG11201609591PA/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/15—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis
    • 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
    • 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
    • B01J31/16—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
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2447—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring
    • B01J31/2452—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom
    • 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
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2461—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring
    • B01J31/2471—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring with more than one complexing phosphine-P atom
    • B01J31/2476—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as ring members in the condensed ring system or in a further ring 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
    • 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
    • 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
    • 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)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (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)
SG11201609591PA 2014-05-16 2015-05-13 Process for preparing an unsaturated carboxylic acid salt SG11201609591PA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14168612 2014-05-16
PCT/EP2015/060535 WO2015173276A1 (en) 2014-05-16 2015-05-13 Process for preparing an unsaturated carboxylic acid salt

Publications (1)

Publication Number Publication Date
SG11201609591PA true SG11201609591PA (en) 2016-12-29

Family

ID=50731956

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201609591PA SG11201609591PA (en) 2014-05-16 2015-05-13 Process for preparing an unsaturated carboxylic acid salt

Country Status (8)

Country Link
US (1) US10011551B2 (en)
EP (1) EP3142992B2 (en)
JP (1) JP6635948B2 (en)
KR (1) KR20170010800A (en)
CN (1) CN106458823B (en)
RU (1) RU2016149428A (en)
SG (1) SG11201609591PA (en)
WO (1) WO2015173276A1 (en)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9725393B2 (en) 2014-10-08 2017-08-08 Chevron Phillips Chemical Company Lp Methods for the production of α,β-unsaturated carboxylic acids and salts thereof
US9416087B2 (en) 2014-10-08 2016-08-16 Chevron Phillips Chemical Company Lp Methods for the production of α,β-unsaturated carboxylic acids and salts thereof
BR112018000606B1 (en) 2015-07-22 2022-01-18 Basf Se PROCESS FOR PREPARATION OF FURAN-2,5-DICARBOXYLIC ACID AND USE OF A CATALYST
BR112018008730A8 (en) 2015-11-04 2019-02-26 Basf Se A process for preparing a mixture and use of a carboxylic acid ester
CA3003762A1 (en) 2015-11-04 2017-05-11 Basf Se A process for preparing furan-2,5-dicarboxylic acid
EP3170828A1 (en) 2015-11-23 2017-05-24 Basf Se Method for the preparation of compounds with 16-oxabicyclo [10.3.1] pentadecen scaffold and their secondary products
CN113402375B (en) 2015-12-15 2024-04-02 切弗朗菲利浦化学公司 Formation of alpha, beta-unsaturated carboxylic acids and salts thereof from metal lactones and anionic polyelectrolytes
CN115433075A (en) * 2016-04-06 2022-12-06 切弗朗菲利浦化学公司 Process for producing alpha, beta-unsaturated carboxylic acids and salts thereof
US10774024B2 (en) * 2016-04-11 2020-09-15 Basf Se Process for preparing an unsaturated carboxylic acid salt
US10550061B2 (en) 2017-06-14 2020-02-04 Chevron Phillips Chemical Company Lp Sulfur oxoacid-substituted and phosphorus oxoacid-substituted polyaromatic resins and salts thereof as promoters in acrylate production from coupling reactions of olefins and carbon dioxide
US20180362435A1 (en) * 2017-06-14 2018-12-20 Chevron Phillips Chemical Company Lp High porosity aromatic resins as promoters in acrylate production from coupling reactions of olefins and carbon dioxide
US10544080B2 (en) 2017-06-14 2020-01-28 Chevron Phillips Chemical Company Lp Continuous process for the conversion of olefins and carbon dioxide to acrylates via solution phase reactor
JP7019912B2 (en) * 2017-12-25 2022-02-16 ピーティーティー グローバル ケミカル パブリック カンパニー リミテッド Catalyst composition for the process of producing unsaturated carboxylates and their derivatives from carbon dioxide and olefins
US11174213B2 (en) * 2018-10-12 2021-11-16 Chevron Phillips Chemical Company, Lp Effects of catalyst concentration and solid activator on nickel-mediated olefin/carbon dioxide coupling to acrylates
CN114956979B (en) * 2022-06-06 2023-04-28 中国科学技术大学 Catalyst system for synthesizing phenylacetic acid from toluene

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4792620A (en) * 1983-10-14 1988-12-20 Bp Chemicals Limited Carbonylation catalysts
US7169953B2 (en) 2001-11-09 2007-01-30 The Penn State Research Foundation P-chiral phospholanes and phosphocyclic compounds and their use in asymmetric catalytic reactions
US7608709B2 (en) 2005-07-25 2009-10-27 National University Corporation Chiba University 2, 3-bis(dialkylphosphino)pyrazine derivative, process of producing the same, and metal complex having the same as ligand
EP2542516A2 (en) * 2010-03-03 2013-01-09 Basf Se Production of ethylenically unsaturated carboxylic acid salts by the carboxylation of alkenes
US8642803B2 (en) * 2010-03-03 2014-02-04 Basf Se Preparation of ethylenically unsaturated carboxylic salts by carboxylation of alkenes
JP6122030B2 (en) * 2011-12-29 2017-04-26 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ Preparation of α, β-ethylenically unsaturated carboxylates by catalytic carboxylation of alkenes
JP2015526414A (en) * 2012-07-17 2015-09-10 ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ Transition metal carbene complex catalyzed process for the preparation of carboxylic acid esters from alcohols under dehydration

Also Published As

Publication number Publication date
KR20170010800A (en) 2017-02-01
EP3142992B2 (en) 2022-02-16
RU2016149428A (en) 2018-06-19
EP3142992A1 (en) 2017-03-22
EP3142992B1 (en) 2018-09-26
JP2017523127A (en) 2017-08-17
WO2015173276A1 (en) 2015-11-19
JP6635948B2 (en) 2020-01-29
US10011551B2 (en) 2018-07-03
CN106458823A (en) 2017-02-22
US20170217869A1 (en) 2017-08-03
CN106458823B (en) 2022-04-19

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