GB316951A - Process for the manufacture of condensation products from olefines and unsaturated hydrocarbons - Google Patents

Process for the manufacture of condensation products from olefines and unsaturated hydrocarbons

Info

Publication number
GB316951A
GB316951A GB24040/29A GB2404029A GB316951A GB 316951 A GB316951 A GB 316951A GB 24040/29 A GB24040/29 A GB 24040/29A GB 2404029 A GB2404029 A GB 2404029A GB 316951 A GB316951 A GB 316951A
Authority
GB
United Kingdom
Prior art keywords
olefines
earth
aromatic
fuller
naphthalene
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
GB24040/29A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB316951A publication Critical patent/GB316951A/en
Expired 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
    • C07C2/54Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
    • C07C2/64Addition to a carbon atom of a six-membered aromatic ring
    • C07C2/66Catalytic processes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/16Clays or other mineral silicates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

316,951. I. G. Farbenindustrie Akt.- Ges. Aug. 4, 1928, [Convention date]. Mineral and tar oils.-Olefines containing at least three carbon atoms in the molecule are condensed with each other or with aromatic hydrocarbons in the presence of a hydrosilicate possessing a large surface and high porosity. Suitable hydrosilicates are those of aluminium and magnesium, such as bleaching earth, Florida earth, and Fuller's earth, to which other condensing agents .may be added, such as a metal halide or an addition compound of an olefine with an aluminium halide. Aromatic hydrocarbons mentioned are benzene and its homologues, polynuclear hydrocarbons such as naphthalene and anthracene, and partially-hydrogenated compounds, such as tetrahydro-naphthalene. As olefinic components may be employed the technical products obtained in the refining of oils by the Edeleanu process. The olefines may also be employed diluted with other gases, e.g. in the form of oil gas or cracking gas. The reaction is facilitated by the use of raised temperature and increased pressure, and also by the presence of hydrogen halides. A solvent may be used. According to one of the examples, a mobile Edeleanu extract is treated in the presence of Fuller's earth with propylene at elevated temperature and pressure, and yields, after vacuum distillation, a bright odourless oil; similar results are obtained by using butylene amylene or cyclohexene. Specifications 291,137 and 296,034, [both in Class 2 (iii), Dyes &c.], are referred to. The Specification as open to inspection under Sect. 91 (3) (a) describes also the condensation of olefines containing at least three carbon atoms with aromatic and aliphatic compounds containing a double bond; phenols are mentioned as suitable aromatic compounds. This subjectmatter does not appear in the Specification as accepted.
GB24040/29A 1928-08-04 1929-08-06 Process for the manufacture of condensation products from olefines and unsaturated hydrocarbons Expired GB316951A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE316951X 1928-08-04

Publications (1)

Publication Number Publication Date
GB316951A true GB316951A (en) 1930-11-06

Family

ID=6150627

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24040/29A Expired GB316951A (en) 1928-08-04 1929-08-06 Process for the manufacture of condensation products from olefines and unsaturated hydrocarbons

Country Status (1)

Country Link
GB (1) GB316951A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2419796A (en) * 1942-07-13 1947-04-29 Phillips Petroleum Co Alkylation process
US2419599A (en) * 1942-10-05 1947-04-29 Phillips Petroleum Co Alkylation of aromatic hydrocarbons
US2930820A (en) * 1957-09-16 1960-03-29 Robert S Aries Alkylation of toluene
US2945072A (en) * 1956-04-11 1960-07-12 Allied Chem Alkylation and dealkylation processes
US4665256A (en) * 1983-04-29 1987-05-12 The Dow Chemical Company Alkylation of aromatic mixtures

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2419796A (en) * 1942-07-13 1947-04-29 Phillips Petroleum Co Alkylation process
US2419599A (en) * 1942-10-05 1947-04-29 Phillips Petroleum Co Alkylation of aromatic hydrocarbons
US2945072A (en) * 1956-04-11 1960-07-12 Allied Chem Alkylation and dealkylation processes
US2930820A (en) * 1957-09-16 1960-03-29 Robert S Aries Alkylation of toluene
US4665256A (en) * 1983-04-29 1987-05-12 The Dow Chemical Company Alkylation of aromatic mixtures

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