GB323100A - Process for the manufacture of condensation products of polynuclear compounds - Google Patents
Process for the manufacture of condensation products of polynuclear compoundsInfo
- Publication number
- GB323100A GB323100A GB3565328A GB3565328A GB323100A GB 323100 A GB323100 A GB 323100A GB 3565328 A GB3565328 A GB 3565328A GB 3565328 A GB3565328 A GB 3565328A GB 323100 A GB323100 A GB 323100A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthalene
- condensed
- olefines
- anthracene
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation 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
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation 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
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
- C07C2/68—Catalytic processes with halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/06—Halogens; Compounds thereof
- C07C2527/125—Compounds comprising a halogen and scandium, yttrium, aluminium, gallium, indium or thallium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
323,100. Carpmael, A., (I. G. Farbenindustrie Akt.-Ges.). Dec. 3, 1928. Homologues of polynuclear compounds. - Isocyclic polynuclear hydrocarbons, partially hydrogenated or other oxygen-free derivatives thereof with the exception of completely hydrogenated aromatic compounds, are caused to react with olefines, or gases containing olefines, in the presence of a catalyst and an inert solvent or diluent. Suitable catalysts are metal halides of the Friedel-Crafts type, boron halide, or addition compounds of aluminium halides with olefines. These catalysts may be combined with substances which tend to facilitate the reaction, such as benzene and gaseous halogen acids. In an example, ethylene at 80-90‹ C. and under a pressure of 20 atmospheres is introduced into a mixture of naphthalene and decahydronaphthalene containing anhydrous aluminium bromide. The product, which is distilled, consists chiefly of a viscous fluorescent oil. Further examples are given in which ethylene is condensed with achloronaphthalene, acenaphthene and anthracene; propylene is condensed with naphthalene tetrahydronophthalene, phenanthrene, crude anthracene, and anthracene residues; #-butylene is condensed with naphthalene; and cylclohexane is condensed with naphthalene. The solvents used in the above examples are decahydronaphthalene, hexahydrotoluene, hexahydrobenzene, and petroleum ether. Specifications 265,601, 273,665, and 316,951 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3565328A GB323100A (en) | 1928-12-03 | 1928-12-03 | Process for the manufacture of condensation products of polynuclear compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3565328A GB323100A (en) | 1928-12-03 | 1928-12-03 | Process for the manufacture of condensation products of polynuclear compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB323100A true GB323100A (en) | 1929-12-24 |
Family
ID=10380093
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3565328A Expired GB323100A (en) | 1928-12-03 | 1928-12-03 | Process for the manufacture of condensation products of polynuclear compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB323100A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2945901A (en) * | 1958-06-06 | 1960-07-19 | Exxon Research Engineering Co | Production of polyisopropyl benzene |
US4604491A (en) * | 1984-11-26 | 1986-08-05 | Koppers Company, Inc. | Synthetic oils |
-
1928
- 1928-12-03 GB GB3565328A patent/GB323100A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2945901A (en) * | 1958-06-06 | 1960-07-19 | Exxon Research Engineering Co | Production of polyisopropyl benzene |
US4604491A (en) * | 1984-11-26 | 1986-08-05 | Koppers Company, Inc. | Synthetic oils |
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