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FR2042477A1 - Catalytic dimerisation of ethylene - Google Patents

Catalytic dimerisation of ethylene

Info

Publication number
FR2042477A1
FR2042477A1 FR7015856A FR7015856A FR2042477A1 FR 2042477 A1 FR2042477 A1 FR 2042477A1 FR 7015856 A FR7015856 A FR 7015856A FR 7015856 A FR7015856 A FR 7015856A FR 2042477 A1 FR2042477 A1 FR 2042477A1
Authority
FR
France
Prior art keywords
atm
ethylene
butene
moles
toluene
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
FR7015856A
Other languages
French (fr)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SnamProgetti SpA
Original Assignee
SnamProgetti SpA
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 SnamProgetti SpA filed Critical SnamProgetti SpA
Publication of FR2042477A1 publication Critical patent/FR2042477A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C07C2/06Preparation 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 alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08Catalytic processes
    • C07C2/26Catalytic processes with hydrides or organic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • C07C2531/14Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

1-Butene is obtained using a catalyst system comprising (a) a reducing Al compound HX Al N (R1) (R2) where R1, R2 independently are 1-10C hydrocarbon and X = H or halogen, e.g. Cl, Br or I and (b) Ti(OR)4 where R4 = 1 - 10C hydrocarbon. Reaction is preferably in a solvent chosen from (cyclo)aliphatic and aromatic hydrocarbons, under 1 - 100 atm. pressure. Example: 5 atm. C2H4 introduced to autoclave at 65 degrees C containing 51.0 m moles H2AlN(CH3)2 in 100 cm3 toluene. 17.0 m moles Ti(O-isoC3H7)4 in 15 cm3 toluene were added. Pressure raised to 20 atm. C2H4; agitation continued for 3 hrs. 94% C2H4 was converted to 1-butene; 0.6 g. high density polyethylene was obtained also.
FR7015856A 1969-05-08 1970-04-30 Catalytic dimerisation of ethylene Withdrawn FR2042477A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT1655069 1969-05-08

Publications (1)

Publication Number Publication Date
FR2042477A1 true FR2042477A1 (en) 1971-02-12

Family

ID=11149025

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7015856A Withdrawn FR2042477A1 (en) 1969-05-08 1970-04-30 Catalytic dimerisation of ethylene

Country Status (5)

Country Link
BE (1) BE750013A (en)
DE (1) DE2022658C3 (en)
FR (1) FR2042477A1 (en)
LU (1) LU60872A1 (en)
NL (1) NL155806B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU681032A1 (en) * 1976-02-23 1979-08-25 Грозненский филиал Охтинского научно-производственного объединения "Пластполимер" Process for the preparation of dimers and codimers of alpha-olefins

Also Published As

Publication number Publication date
DE2022658B2 (en) 1973-02-22
DE2022658C3 (en) 1973-09-20
NL7006562A (en) 1970-11-10
LU60872A1 (en) 1970-07-09
DE2022658A1 (en) 1970-11-19
BE750013A (en) 1970-10-16
NL155806B (en) 1978-02-15

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Legal Events

Date Code Title Description
TP Transmission of property
ST Notification of lapse