BR112016013233A2 - Processo para telomerização de butadieno - Google Patents

Processo para telomerização de butadieno

Info

Publication number
BR112016013233A2
BR112016013233A2 BR112016013233A BR112016013233A BR112016013233A2 BR 112016013233 A2 BR112016013233 A2 BR 112016013233A2 BR 112016013233 A BR112016013233 A BR 112016013233A BR 112016013233 A BR112016013233 A BR 112016013233A BR 112016013233 A2 BR112016013233 A2 BR 112016013233A2
Authority
BR
Brazil
Prior art keywords
butadiene
telomization
telomerization
alkanols
octadiene
Prior art date
Application number
BR112016013233A
Other languages
English (en)
Other versions
BR112016013233B1 (pt
Inventor
N Launay Helene
L Klinkenberg Jessica
r briggs John
E House Sarah
C Van Engelen Marcel
G Wright Larry
Bar Georg
Hansen Wilma
Fuertes Cabello Julia
Lengyel Istvan
Original Assignee
Dow Global Technologies 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 Dow Global Technologies Llc filed Critical Dow Global Technologies Llc
Publication of BR112016013233A2 publication Critical patent/BR112016013233A2/pt
Publication of BR112016013233B1 publication Critical patent/BR112016013233B1/pt

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
    • B01J31/24Phosphines, 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
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2419Cyclic 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
    • B01J31/2438Cyclic 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 and further hetero atoms as ring members, excluding the positions adjacent to P
    • 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
    • B01J31/24Phosphines, 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
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442Cyclic 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
    • B01J31/2461Cyclic 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
    • B01J31/248Bridged ring systems, e.g. 9-phosphabicyclononane
    • B01J31/2485Tricyclic systems, e.g. phosphaadamantanes and hetero analogues
    • 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
    • B01J31/24Phosphines, 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
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/38Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of dienes or alkynes
    • C07C2/40Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of dienes or alkynes of conjugated dienes
    • C07C2/403Catalytic processes
    • C07C2/406Catalytic processes with hydrides or organic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/006Palladium compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/20Olefin oligomerisation or telomerisation
    • 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
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0238Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
    • 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
    • B01J2531/824Palladium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/24Phosphines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

PROCESSO PARA TELOMERIZAÇÃO DE BUTADIENO. Uso de uma mistura de solvente que contém 1-metoxi-2,7-octadieno e alcanóis ao invés de alcanóis por si mesmos para preparar um precursor de catalisador adequado para uso na telomerização de butadieno.
BR112016013233-5A 2013-12-13 2014-12-04 processo para telomerização de butadieno BR112016013233B1 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361915781P 2013-12-13 2013-12-13
US61/915,781 2013-12-13
PCT/US2014/068483 WO2015088867A2 (en) 2013-12-13 2014-12-04 Butadiene telomerization catalyst precursor preparation

Publications (2)

Publication Number Publication Date
BR112016013233A2 true BR112016013233A2 (pt) 2017-08-08
BR112016013233B1 BR112016013233B1 (pt) 2021-05-04

Family

ID=52347391

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112016013233-5A BR112016013233B1 (pt) 2013-12-13 2014-12-04 processo para telomerização de butadieno

Country Status (7)

Country Link
US (2) US10569262B2 (pt)
EP (2) EP3741769B1 (pt)
CN (1) CN105813743B (pt)
BR (1) BR112016013233B1 (pt)
CA (2) CA3133814C (pt)
ES (2) ES2953829T3 (pt)
WO (1) WO2015088867A2 (pt)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3133814C (en) 2013-12-13 2024-05-21 Dow Global Technologies Llc Butadiene telomerization catalyst precursor preparation
EP3280690B1 (en) 2015-04-10 2019-06-19 Dow Global Technologies LLC Butadiene telomerization catalyst and preparation thereof

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU7919182A (en) * 1981-01-19 1982-07-29 Goodyear Aerospace Corp. Parking brake
IT1240737B (it) 1990-04-02 1993-12-17 Snam Progetti Sistema catalitico e procedimento per la produzione selettiva di isoprenil-alchileteri da isoprene
CA2097297C (en) * 1990-12-13 2000-11-07 Robert C. Bohley Process for producing 1-octene
EP2321244B1 (en) 2008-08-12 2016-12-21 Dow Global Technologies LLC Improved process for telomerization of butadiene
US9174905B2 (en) 2010-12-21 2015-11-03 Dow Global Technologies Llc Process for telomerization of butadiene using a mono-orthoalkoxy substituted catalyst
CA3133814C (en) 2013-12-13 2024-05-21 Dow Global Technologies Llc Butadiene telomerization catalyst precursor preparation
EP3280690B1 (en) 2015-04-10 2019-06-19 Dow Global Technologies LLC Butadiene telomerization catalyst and preparation thereof

Also Published As

Publication number Publication date
US20200147596A1 (en) 2020-05-14
CA3133814A1 (en) 2015-06-18
US10751706B2 (en) 2020-08-25
EP3741769B1 (en) 2023-06-28
ES2836348T3 (es) 2021-06-24
WO2015088867A2 (en) 2015-06-18
ES2953829T3 (es) 2023-11-16
US10569262B2 (en) 2020-02-25
CA3133814C (en) 2024-05-21
CA2933342A1 (en) 2015-06-18
CN105813743B (zh) 2019-06-21
EP3741769A1 (en) 2020-11-25
CN105813743A (zh) 2016-07-27
EP3080136A2 (en) 2016-10-19
CA2933342C (en) 2021-11-09
WO2015088867A3 (en) 2015-11-12
US20160271601A1 (en) 2016-09-22
BR112016013233B1 (pt) 2021-05-04
EP3080136B1 (en) 2020-10-28

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Legal Events

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B06U Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]

Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 04/12/2014, OBSERVADAS AS CONDICOES LEGAIS.