GB1120256A - Process for the production of oxirane compounds and phthalic anhydride or alpha-naphthol - Google Patents
Process for the production of oxirane compounds and phthalic anhydride or alpha-naphtholInfo
- Publication number
- GB1120256A GB1120256A GB4660965A GB4660965A GB1120256A GB 1120256 A GB1120256 A GB 1120256A GB 4660965 A GB4660965 A GB 4660965A GB 4660965 A GB4660965 A GB 4660965A GB 1120256 A GB1120256 A GB 1120256A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tetralol
- naphthol
- phthalic anhydride
- oxirane
- tetralin
- 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
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 title abstract 4
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 title abstract 4
- 150000002924 oxiranes Chemical class 0.000 title abstract 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 title 2
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 abstract 9
- 239000003054 catalyst Substances 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000006356 dehydrogenation reaction Methods 0.000 abstract 3
- 238000006735 epoxidation reaction Methods 0.000 abstract 3
- 230000003647 oxidation Effects 0.000 abstract 3
- 238000007254 oxidation reaction Methods 0.000 abstract 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 229910001882 dioxygen Inorganic materials 0.000 abstract 2
- 239000007791 liquid phase Substances 0.000 abstract 2
- 229910052750 molybdenum Inorganic materials 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- 229910052720 vanadium Inorganic materials 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052770 Uranium Inorganic materials 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000005609 naphthenate group Chemical group 0.000 abstract 1
- 229910052758 niobium Inorganic materials 0.000 abstract 1
- 239000012071 phase Substances 0.000 abstract 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229910052702 rhenium Inorganic materials 0.000 abstract 1
- 229910052711 selenium Inorganic materials 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229910052715 tantalum Inorganic materials 0.000 abstract 1
- 229910052719 titanium Inorganic materials 0.000 abstract 1
- 229910052721 tungsten Inorganic materials 0.000 abstract 1
- 229910052726 zirconium Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/19—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic hydroperoxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
- C07C39/14—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings with at least one hydroxy group on a condensed ring system containing two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/31—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting
- C07C51/313—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting with molecular oxygen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Epoxy Compounds (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Manufacture And Refinement Of Metals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41001064A | 1964-11-09 | 1964-11-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1120256A true GB1120256A (en) | 1968-07-17 |
Family
ID=23622845
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4660965A Expired GB1120256A (en) | 1964-11-09 | 1965-11-03 | Process for the production of oxirane compounds and phthalic anhydride or alpha-naphthol |
Country Status (10)
Country | Link |
---|---|
BE (1) | BE671143A (enrdf_load_stackoverflow) |
CH (2) | CH461453A (enrdf_load_stackoverflow) |
DE (1) | DE1543029A1 (enrdf_load_stackoverflow) |
DK (1) | DK116727B (enrdf_load_stackoverflow) |
ES (1) | ES319383A1 (enrdf_load_stackoverflow) |
GB (1) | GB1120256A (enrdf_load_stackoverflow) |
IL (1) | IL24593A (enrdf_load_stackoverflow) |
LU (1) | LU49691A1 (enrdf_load_stackoverflow) |
NO (1) | NO121038B (enrdf_load_stackoverflow) |
SE (1) | SE335117B (enrdf_load_stackoverflow) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19519004A1 (de) * | 1995-05-24 | 1996-11-28 | Hoechst Ag | Neue selen- und rutheniumhaltige Metalloxidkatalysatoren sowie ein Verfahren zu ihrer Herstellung und ihre Verwendung |
DE19519008A1 (de) * | 1995-05-24 | 1996-11-28 | Hoechst Ag | Neue ruthenium- und selen- oder schwefelhaltige Metalloxidkatalysatoren sowie ein Verfahren zu ihrer Herstellung und ihre Verwendung |
-
1965
- 1965-10-20 BE BE671143D patent/BE671143A/xx unknown
- 1965-10-22 LU LU49691D patent/LU49691A1/xx unknown
- 1965-11-03 GB GB4660965A patent/GB1120256A/en not_active Expired
- 1965-11-08 DK DK573265A patent/DK116727B/da unknown
- 1965-11-08 IL IL2459365A patent/IL24593A/en unknown
- 1965-11-09 CH CH1498967A patent/CH461453A/fr unknown
- 1965-11-09 SE SE1443665A patent/SE335117B/xx unknown
- 1965-11-09 NO NO16040365A patent/NO121038B/no unknown
- 1965-11-09 CH CH1542965A patent/CH450384A/fr unknown
- 1965-11-09 ES ES0319383A patent/ES319383A1/es not_active Expired
- 1965-11-09 DE DE19651543029 patent/DE1543029A1/de active Pending
Also Published As
Publication number | Publication date |
---|---|
IL24593A (en) | 1969-07-30 |
BE671143A (enrdf_load_stackoverflow) | 1966-04-20 |
NO121038B (enrdf_load_stackoverflow) | 1971-01-11 |
CH461453A (fr) | 1968-08-31 |
DK116727B (da) | 1970-02-09 |
ES319383A1 (es) | 1966-05-01 |
LU49691A1 (enrdf_load_stackoverflow) | 1967-04-24 |
DE1543029A1 (de) | 1969-09-11 |
SE335117B (enrdf_load_stackoverflow) | 1971-05-17 |
CH450384A (fr) | 1968-01-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1420662A (en) | Process for the splitting by oxidation of unsaturated hydro carbons | |
ES298676A1 (es) | Un procedimiento para la preparacion de aldehidos o cetonas | |
US2393240A (en) | Improvements in exothermic chemical reactions | |
GB1016900A (en) | Oxidation of olefins to epoxy-alcohols | |
JPH04210932A (ja) | tert−ブチルヒドロペルオキシドからtert−ブチルアルコールの触媒的製造法 | |
GB1120256A (en) | Process for the production of oxirane compounds and phthalic anhydride or alpha-naphthol | |
US3340304A (en) | Selective oxidation of cyclohexane to cyclohexanone | |
GB864803A (en) | Process for the manufacture of percarboxylic acids | |
DE1196646B (de) | Verfahren zur Herstellung von Cyclododecanol | |
Tanaka et al. | Photo-assisted oxidation of 2-methylpropane over Rb+-modified V2O5/SiO2. Formation of 2-methylpropane-2-ol from 2-methylpropane and O2 | |
GB1209321A (en) | Process for the production of epoxides | |
US10703700B2 (en) | Liquid phase oxidation of lower alkanes to oxygenates | |
US3840594A (en) | Process for preparing mesitylenic acid | |
Dimitratos et al. | Supported metal nanoparticles in liquid-phase oxidation reactions | |
GB1044752A (en) | Preparation of dicarboxylic acids by nitric acid oxidation | |
US3042722A (en) | Oxidation of cyclic olefins | |
GB1107292A (en) | The preparation of ªŠ-caprolactone | |
Subrahmanyam et al. | Pyridinealdehydes preparation by vapour phase oxidation of 2-and 3-pyridenemethanols and of their N-oxides on a V-Mo oxide catalyst | |
GB716820A (en) | Preparation of oxidized cyclohexane | |
GB947555A (en) | A process for carrying out liquid phase oxidations of cycloparaffins | |
US3987103A (en) | Preparation of isopropanol and acetone | |
US4263447A (en) | Preparation of allylic cycloalkenols and carboxylic acid esters thereof | |
DE1468012B2 (de) | Verfahren zur herstellung von epoxyverbindungen | |
US2021127A (en) | Preparation of organic acids | |
GB1115220A (en) | Production of oxirane compounds |