SG11201705237XA - Use of a ruthenium promoter in a phosphine oxide carbonylation process - Google Patents

Use of a ruthenium promoter in a phosphine oxide carbonylation process

Info

Publication number
SG11201705237XA
SG11201705237XA SG11201705237XA SG11201705237XA SG11201705237XA SG 11201705237X A SG11201705237X A SG 11201705237XA SG 11201705237X A SG11201705237X A SG 11201705237XA SG 11201705237X A SG11201705237X A SG 11201705237XA SG 11201705237X A SG11201705237X A SG 11201705237XA
Authority
SG
Singapore
Prior art keywords
phosphine oxide
carbonylation process
ruthenium promoter
oxide carbonylation
ruthenium
Prior art date
Application number
SG11201705237XA
Inventor
Noel C Hallinan
David L Ramage
Daniel F White
Original Assignee
Lyondellbasell Acetyls Llc
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
Application filed by Lyondellbasell Acetyls Llc filed Critical Lyondellbasell Acetyls Llc
Publication of SG11201705237XA publication Critical patent/SG11201705237XA/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/223At least two oxygen atoms present in one at least bidentate or bridging ligand
    • B01J31/2239Bridging ligands, e.g. OAc in Cr2(OAc)4, Pt4(OAc)8 or dicarboxylate ligands
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0255Phosphorus containing compounds
    • B01J31/0257Phosphorus acids or phosphorus acid esters
    • B01J31/0262Phosphorus acids or phosphorus acid esters comprising phosphinous acid (-ester) groups (R2P(OR')) or the isomeric phosphine oxide groups (R3P=O), i.e. R= C, R'= C, H
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C07C51/12Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/50Use of additives, e.g. for stabilisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • C07C53/08Acetic acid
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/822Rhodium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
SG11201705237XA 2015-01-20 2016-01-18 Use of a ruthenium promoter in a phosphine oxide carbonylation process SG11201705237XA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562105572P 2015-01-20 2015-01-20
PCT/US2016/013790 WO2016118448A1 (en) 2015-01-20 2016-01-18 Use of a ruthenium promoter in a phosphine oxide carbonylation process

Publications (1)

Publication Number Publication Date
SG11201705237XA true SG11201705237XA (en) 2017-07-28

Family

ID=55305077

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201705237XA SG11201705237XA (en) 2015-01-20 2016-01-18 Use of a ruthenium promoter in a phosphine oxide carbonylation process

Country Status (7)

Country Link
US (1) US9822054B2 (en)
EP (1) EP3247694B1 (en)
KR (1) KR101918885B1 (en)
CN (2) CN112759511A (en)
BR (1) BR112017014875A2 (en)
SG (1) SG11201705237XA (en)
WO (1) WO2016118448A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109408846B (en) 2017-08-18 2024-03-08 三星电子株式会社 Integrated circuit, non-transitory computer readable medium, and computing system

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0072055B1 (en) 1981-08-06 1985-05-02 Shell Internationale Researchmaatschappij B.V. Process for the co-production of carboxylic acids and carboxylic acid esters
US4640802A (en) * 1981-12-10 1987-02-03 Shell Oil Company Process for the co-production of carboxylic acids and carboxylic acid esters
CA1194033A (en) * 1981-12-10 1985-09-24 Eit Drent Process for the co-production of carboxylic acids and carboxylic acid esters
US5817869A (en) 1995-10-03 1998-10-06 Quantum Chemical Corporation Use of pentavalent Group VA oxides in acetic acid processing
US6031129A (en) 1995-10-03 2000-02-29 Quantum Chemical Corporation Use of pentavalent group VA oxides in acetic acid processing
AU3703199A (en) 1998-03-31 1999-10-18 Haldor Topsoe A/S Process for production of acetic acid
CN1113845C (en) * 1998-05-27 2003-07-09 千年石油化工公司 Use of pentavalent group VA oxides in acetic acid processing
GB9926855D0 (en) * 1999-11-12 2000-01-12 Bp Chem Int Ltd Process
GB0311091D0 (en) 2003-05-14 2003-06-18 Bp Chem Int Ltd Process
US7053241B1 (en) 2005-02-24 2006-05-30 Celanese International Corporation Acetic acid production methods incorporating at least one metal salt as a catalyst stabilizer
US9024061B2 (en) * 2010-06-14 2015-05-05 Celanese International Corporation Methanol carbonylation process with rhodium catalyst and a metallic co-catalyst selected from transition metals, zinc, beryllium, indium, tin, strontium and barium
CN102320950B (en) * 2011-09-28 2015-05-13 上海华谊(集团)公司 Method for synthesizing acetic acid through carbonylation

Also Published As

Publication number Publication date
WO2016118448A9 (en) 2017-07-27
CN112759511A (en) 2021-05-07
EP3247694A1 (en) 2017-11-29
KR20170104520A (en) 2017-09-15
CN107207393A (en) 2017-09-26
BR112017014875A2 (en) 2018-03-13
US9822054B2 (en) 2017-11-21
WO2016118448A1 (en) 2016-07-28
US20160207863A1 (en) 2016-07-21
EP3247694B1 (en) 2020-08-19
KR101918885B1 (en) 2018-11-14

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