ES378132A1 - A process for epoxidizing olefins with organic hydroperoxides - Google Patents

A process for epoxidizing olefins with organic hydroperoxides

Info

Publication number
ES378132A1
ES378132A1 ES378132A ES378132A ES378132A1 ES 378132 A1 ES378132 A1 ES 378132A1 ES 378132 A ES378132 A ES 378132A ES 378132 A ES378132 A ES 378132A ES 378132 A1 ES378132 A1 ES 378132A1
Authority
ES
Spain
Prior art keywords
organic hydroperoxides
olefinic
carbon atoms
octene
olefinic compounds
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.)
Expired
Application number
ES378132A
Other languages
Spanish (es)
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.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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 Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of ES378132A1 publication Critical patent/ES378132A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D301/00Preparation of oxiranes
    • C07D301/02Synthesis of the oxirane ring
    • C07D301/03Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
    • C07D301/19Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic hydroperoxides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/20Vanadium, niobium or tantalum
    • B01J23/22Vanadium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/04Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Epoxy Compounds (AREA)

Abstract

Epoxides are produced by reacting one or more olefinic compounds with one or more organic hydroperoxides using a catalyst which is insoluble in the reaction mixture and comprising vanadium in chemical combination with a solid silica and/or inorganic silicate. The preferred olefinic starting materials are olefinic hydrocarbons having 2-10 carbon atoms, butadiene, and olefinic compounds substituted by hydroxy groups or halogens, e.g. allyl alcohol, crotyl alcohol and allyl chloride. Suitable organic hydroperoxides are those of formula ROOH in which R is a C 3 -C 20 hydrocarbon group, in particular a secondary or tertiary alkyl or an aralkyl group of 3-10 carbon atoms. Examples describe the preparation of 1-octene oxide from 1-octene and t-butylhydroperoxide.
ES378132A 1969-04-02 1970-04-01 A process for epoxidizing olefins with organic hydroperoxides Expired ES378132A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US81292469A 1969-04-02 1969-04-02

Publications (1)

Publication Number Publication Date
ES378132A1 true ES378132A1 (en) 1972-05-16

Family

ID=25210980

Family Applications (1)

Application Number Title Priority Date Filing Date
ES378132A Expired ES378132A1 (en) 1969-04-02 1970-04-01 A process for epoxidizing olefins with organic hydroperoxides

Country Status (14)

Country Link
JP (1) JPS5030051B1 (en)
AT (1) AT302987B (en)
BE (1) BE748317A (en)
BR (1) BR7017927D0 (en)
CH (1) CH529125A (en)
DE (1) DE2015542C3 (en)
DK (1) DK133749B (en)
ES (1) ES378132A1 (en)
FR (1) FR2042773A5 (en)
GB (1) GB1248709A (en)
IE (1) IE34080B1 (en)
NL (1) NL145234B (en)
NO (1) NO127503B (en)
SE (1) SE361171B (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3391213A (en) * 1967-06-12 1968-07-02 Shell Oil Co Isoprene production from isopentane via hydroperoxide and borate ester

Also Published As

Publication number Publication date
DK133749B (en) 1976-07-12
DE2015542B2 (en) 1979-11-29
DE2015542A1 (en) 1970-10-08
NL145234B (en) 1975-03-17
SE361171B (en) 1973-10-22
IE34080B1 (en) 1975-01-22
GB1248709A (en) 1971-10-06
FR2042773A5 (en) 1971-02-12
DK133749C (en) 1976-11-29
JPS5030051B1 (en) 1975-09-29
DE2015542C3 (en) 1980-08-07
NO127503B (en) 1973-07-02
AT302987B (en) 1972-11-10
BR7017927D0 (en) 1973-01-11
CH529125A (en) 1972-10-15
IE34080L (en) 1970-10-02
BE748317A (en) 1970-10-01
NL7004584A (en) 1970-10-06

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