GB694961A - Improvements in or relating to the conversion of phenanthrene to anthracene - Google Patents
Improvements in or relating to the conversion of phenanthrene to anthraceneInfo
- Publication number
- GB694961A GB694961A GB12105/50A GB1210550A GB694961A GB 694961 A GB694961 A GB 694961A GB 12105/50 A GB12105/50 A GB 12105/50A GB 1210550 A GB1210550 A GB 1210550A GB 694961 A GB694961 A GB 694961A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sym
- isomerization
- octahydroanthracene
- octahydrophenanthrene
- phenanthrene
- 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
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 title abstract 8
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 title abstract 6
- 238000006243 chemical reaction Methods 0.000 title abstract 2
- 238000006317 isomerization reaction Methods 0.000 abstract 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
- 238000006356 dehydrogenation reaction Methods 0.000 abstract 2
- 238000005984 hydrogenation reaction Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
- 239000001117 sulphuric acid Substances 0.000 abstract 2
- 235000011149 sulphuric acid Nutrition 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 238000005260 corrosion Methods 0.000 abstract 1
- 230000007797 corrosion Effects 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 238000004508 fractional distillation Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 229910001510 metal chloride Inorganic materials 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/27—Polycyclic condensed hydrocarbons containing three rings
- C07C15/28—Anthracenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2702—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously
- C07C5/271—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously with inorganic acids; with salts or anhydrides of acids
- C07C5/2718—Acids of halogen; Salts thereof; complexes thereof with organic compounds
- C07C5/2721—Metal halides; Complexes thereof with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
- C07C7/17—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound with acids or sulfur oxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/24—Anthracenes; Hydrogenated anthracenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE503246D BE503246A (enExample) | 1950-05-15 | ||
| GB12105/50A GB694961A (en) | 1950-05-15 | 1950-05-15 | Improvements in or relating to the conversion of phenanthrene to anthracene |
| FR1036924D FR1036924A (fr) | 1950-05-15 | 1951-05-09 | Perfectionnements apportés aux procédés pour la conversion de phenanthrène en anthracène |
| DEP5530A DE857042C (de) | 1950-05-15 | 1951-05-11 | Verfahren zur Umwandlung von Phenanthren in Anthracen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB12105/50A GB694961A (en) | 1950-05-15 | 1950-05-15 | Improvements in or relating to the conversion of phenanthrene to anthracene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB694961A true GB694961A (en) | 1953-07-29 |
Family
ID=9998479
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB12105/50A Expired GB694961A (en) | 1950-05-15 | 1950-05-15 | Improvements in or relating to the conversion of phenanthrene to anthracene |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE503246A (enExample) |
| DE (1) | DE857042C (enExample) |
| FR (1) | FR1036924A (enExample) |
| GB (1) | GB694961A (enExample) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3336407A (en) * | 1964-02-27 | 1967-08-15 | Sun Oil Co | Catalytic conversion of 1, 2, 3, 4-tetrahydronaphthalene, indan, and other materials |
| US3389188A (en) * | 1966-04-21 | 1968-06-18 | Koppers Co Inc | Process for preparing anthracene from phenanthrene |
| US4367360A (en) * | 1981-09-18 | 1983-01-04 | Koppers Company, Inc. | Method for product isolation and catalyst recovery in aluminum chloride catalyzed isomerization of sym-octahydrophenanthrene to sym-octahydroanthracene |
| US4376224A (en) * | 1982-04-26 | 1983-03-08 | Koppers Company, Inc. | Aluminum chloride catalyzed isomerization of sym-octahydrophenanthrene to sym-octahydroanthracene with acyl peroxide |
| US4376223A (en) * | 1982-04-26 | 1983-03-08 | Koppers Company, Inc. | Method for promoting aluminum chloride catalyzed isomerization of sym octahydrophenanthrene to sym-octahydroanthracene with aryl phenone |
| US4384152A (en) * | 1979-12-22 | 1983-05-17 | Bergwerksverband Gmbh | Anthracene production from phenanthrene |
| US4384156A (en) * | 1982-03-05 | 1983-05-17 | Koppers Company, Inc. | Method for promoting aluminum chloride catalyzed isomerization of sym-octahydrophenanthrene to sym-octahydroanthracene with aroyl halide |
| US4385194A (en) * | 1982-03-05 | 1983-05-24 | Koppers Company, Inc. | Method for promoting aluminum chloride catalyzed isomerization of _sym-octahydrophenanthrene to sym-octahydroanthracene with aralkyl halide |
-
0
- BE BE503246D patent/BE503246A/xx unknown
-
1950
- 1950-05-15 GB GB12105/50A patent/GB694961A/en not_active Expired
-
1951
- 1951-05-09 FR FR1036924D patent/FR1036924A/fr not_active Expired
- 1951-05-11 DE DEP5530A patent/DE857042C/de not_active Expired
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3336407A (en) * | 1964-02-27 | 1967-08-15 | Sun Oil Co | Catalytic conversion of 1, 2, 3, 4-tetrahydronaphthalene, indan, and other materials |
| US3389188A (en) * | 1966-04-21 | 1968-06-18 | Koppers Co Inc | Process for preparing anthracene from phenanthrene |
| US4384152A (en) * | 1979-12-22 | 1983-05-17 | Bergwerksverband Gmbh | Anthracene production from phenanthrene |
| US4367360A (en) * | 1981-09-18 | 1983-01-04 | Koppers Company, Inc. | Method for product isolation and catalyst recovery in aluminum chloride catalyzed isomerization of sym-octahydrophenanthrene to sym-octahydroanthracene |
| US4384156A (en) * | 1982-03-05 | 1983-05-17 | Koppers Company, Inc. | Method for promoting aluminum chloride catalyzed isomerization of sym-octahydrophenanthrene to sym-octahydroanthracene with aroyl halide |
| US4385194A (en) * | 1982-03-05 | 1983-05-24 | Koppers Company, Inc. | Method for promoting aluminum chloride catalyzed isomerization of _sym-octahydrophenanthrene to sym-octahydroanthracene with aralkyl halide |
| US4376224A (en) * | 1982-04-26 | 1983-03-08 | Koppers Company, Inc. | Aluminum chloride catalyzed isomerization of sym-octahydrophenanthrene to sym-octahydroanthracene with acyl peroxide |
| US4376223A (en) * | 1982-04-26 | 1983-03-08 | Koppers Company, Inc. | Method for promoting aluminum chloride catalyzed isomerization of sym octahydrophenanthrene to sym-octahydroanthracene with aryl phenone |
Also Published As
| Publication number | Publication date |
|---|---|
| DE857042C (de) | 1952-11-27 |
| FR1036924A (fr) | 1953-09-14 |
| BE503246A (enExample) |
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