GB1164648A - Preparation of 1,2-Di(aryl)ethylenes - Google Patents
Preparation of 1,2-Di(aryl)ethylenesInfo
- Publication number
- GB1164648A GB1164648A GB46914/66A GB4691466A GB1164648A GB 1164648 A GB1164648 A GB 1164648A GB 46914/66 A GB46914/66 A GB 46914/66A GB 4691466 A GB4691466 A GB 4691466A GB 1164648 A GB1164648 A GB 1164648A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aryl
- oxidant
- reaction
- ethylenes
- stilbene
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/62—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems having two or more ring systems containing condensed 1,3-oxazole rings
- C07D263/64—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems having two or more ring systems containing condensed 1,3-oxazole rings linked in positions 2 and 2' by chains containing six-membered aromatic rings or ring systems containing such rings
-
- 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
- C07C2/76—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen
- C07C2/82—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen oxidative coupling
- C07C2/84—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen oxidative coupling catalytic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/20—Two benzimidazolyl-2 radicals linked together directly or via a hydrocarbon or substituted hydrocarbon radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
- C07D277/66—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/18—Arsenic, antimony or bismuth
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/32—Manganese, technetium or rhenium
- C07C2523/34—Manganese
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,164,648. 1,2-Di-(aryl) ethylenes. EASTMAN KODAK CO. 20 Oct., 1966 [20 Oct., 1965], No. 46914/66. Heading C5E. [Also in Division C2] 1,2-Di-(aryl) ethylenes are prepared by heating one or more mono-aryl methanes at reaction temperatures with, as an inorganic oxidant, As 2 O 5 , Sb 2 O 5 , Bi 2 O 3 , SbO 4 or manganese arsenate or mixtures thereof, or a substance or substances giving rise to said oxidant on heating at or below said reaction temperature. Reaction may be effected at 200-600 C. with the monoaryl methane in liquid or vapour form. The inorganic oxidant may be supported on e.g. alumina, silica, titania or kieselguhr and may be re-oxidized periodically or by continuous or intermittent removal of part of the oxidant during the reaction, re-oxidation thereof and return thereof continuously or intermittently. The preparation of stilbene is described in Examples 1, 2 and 11. 4,4<SP>1</SP>-Diphenyl-stilbene, 1 - naphthyl - 2 - phenyl - ethylene and 1- (naphth - 2<SP>1</SP> - yl) - 2 - naphthylethylene are also specified as products of the process.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49906265A | 1965-10-20 | 1965-10-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1164648A true GB1164648A (en) | 1969-09-17 |
Family
ID=23983664
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB46914/66A Expired GB1164648A (en) | 1965-10-20 | 1966-10-20 | Preparation of 1,2-Di(aryl)ethylenes |
Country Status (2)
Country | Link |
---|---|
US (1) | US3476747A (en) |
GB (1) | GB1164648A (en) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3761536A (en) * | 1971-12-16 | 1973-09-25 | Gulf Research Development Co | Process for coupling propylene and isobutylene |
JPS5745726B2 (en) * | 1974-01-02 | 1982-09-29 | ||
US3965206A (en) * | 1974-01-02 | 1976-06-22 | Monsanto Company | Production of stilbene and styrene |
CH603513A5 (en) * | 1975-02-05 | 1978-08-15 | Sandoz Ag | |
US4196229A (en) * | 1975-02-05 | 1980-04-01 | Sandoz Ltd. | Substituted divinyl stilbenes as optical brighteners |
US4183828A (en) * | 1976-10-27 | 1980-01-15 | Monsanto Company | Catalyst for dehydrocoupling process |
US4091044A (en) * | 1976-10-27 | 1978-05-23 | Monsanto Company | Dehydrocoupling process |
US4117021A (en) * | 1977-05-27 | 1978-09-26 | Gulf Research & Development Company | Process for removing organic oxygen-containing impurities from an organic composition |
US4104318A (en) * | 1977-05-27 | 1978-08-01 | Gulf Research & Development Company | Process for removing organic oxygen-containing impurities from an organic composition in the presence of steam |
US4247727A (en) * | 1979-12-10 | 1981-01-27 | Monsanto Company | Dehydrocoupling of toluene |
US4254293A (en) * | 1979-12-10 | 1981-03-03 | Monsanto Company | Dehydrocoupling of toluene |
US4255604A (en) * | 1979-12-10 | 1981-03-10 | Monsanto Company | Dehydrocoupling of toluene |
US4268704A (en) * | 1979-12-10 | 1981-05-19 | Monsanto Company | Dehydrocoupling of toluene |
US4278824A (en) * | 1979-12-10 | 1981-07-14 | Monsanto Company | Dehydrocoupling of toluene |
US4255602A (en) * | 1979-12-10 | 1981-03-10 | Monsanto Company | Stilbene formation by means of toluene dehydrocoupling using a cobalt-lanthanide catalyst |
DE3062083D1 (en) * | 1979-12-10 | 1983-03-24 | Monsanto Co | Dehydrocoupling of toluene |
US4278826A (en) * | 1979-12-10 | 1981-07-14 | Monsanto Company | Dehydrocoupling of toluene |
US4255603A (en) * | 1979-12-10 | 1981-03-10 | Monsanto Company | Dehydrocoupling of toluene |
US4243825A (en) * | 1979-12-10 | 1981-01-06 | Monsanto Company | Dehydrocoupling of toluene |
US4278825A (en) * | 1979-12-10 | 1981-07-14 | Monsanto Company | Dehydrocoupling of toluene |
US4268703A (en) * | 1979-12-10 | 1981-05-19 | Monsanto Company | Dehydrocoupling of toluene |
JPS58119342A (en) * | 1981-12-29 | 1983-07-15 | Kureha Chem Ind Co Ltd | Catalyst for oxidative dehydrogenating dimerization |
US4921964A (en) * | 1989-03-01 | 1990-05-01 | Eastman Kodak Company | Process for the preparation of stilbene derivatives |
CN102070551B (en) * | 2010-12-29 | 2012-06-20 | 河北星宇化工有限公司 | Method for preparing 2,2'-(1,2-Ethenediyldi-4,1-phenylene)bisbenzoxazole |
PL227854B1 (en) * | 2014-09-07 | 2018-01-31 | Uniwersytet Jagiellonski | Application of 2-(4-styrylphenyl) benzoxazole and polymer scintillator |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2483392A (en) * | 1949-10-04 | Substituted ethylenes and process | ||
GB861240A (en) * | 1958-03-14 | 1961-02-15 | Sterling Drug Inc | Process for the preparation of 4,4-bis(benzimidazol-2-yl) stilbene |
GB999056A (en) * | 1963-08-13 | 1965-07-21 | Distillers Co Yeast Ltd | Improvements in or relating to the production of alkenyl benzenes |
CH469782A (en) * | 1963-11-14 | 1969-03-15 | Ciba Geigy | Use of new bis-oxazolyl-stilbene compounds as optical brightening agents outside the textile industry |
-
1965
- 1965-10-20 US US499062A patent/US3476747A/en not_active Expired - Lifetime
-
1966
- 1966-10-20 GB GB46914/66A patent/GB1164648A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US3476747A (en) | 1969-11-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PLNP | Patent lapsed through nonpayment of renewal fees |