ATE238980T1 - Herstellung von methyl isobutyl und diisobutyl keton - Google Patents
Herstellung von methyl isobutyl und diisobutyl ketonInfo
- Publication number
- ATE238980T1 ATE238980T1 AT97941628T AT97941628T ATE238980T1 AT E238980 T1 ATE238980 T1 AT E238980T1 AT 97941628 T AT97941628 T AT 97941628T AT 97941628 T AT97941628 T AT 97941628T AT E238980 T1 ATE238980 T1 AT E238980T1
- Authority
- AT
- Austria
- Prior art keywords
- dibk
- dmk
- mibk
- ipa
- methyl isobutyl
- Prior art date
Links
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 title abstract 5
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- -1 METHYL ISOBUTYL Chemical compound 0.000 title 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 abstract 2
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 238000005882 aldol condensation reaction Methods 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000004064 recycling 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C07C45/73—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with hydrogenation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US1997/016340 WO1999014177A1 (en) | 1997-09-16 | 1997-09-16 | Manufacture of methyl isobutyl and diisobutyl ketone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE238980T1 true ATE238980T1 (de) | 2003-05-15 |
Family
ID=22261626
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT97941628T ATE238980T1 (de) | 1997-09-16 | 1997-09-16 | Herstellung von methyl isobutyl und diisobutyl keton |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1017661B1 (de) |
| AT (1) | ATE238980T1 (de) |
| AU (1) | AU4349797A (de) |
| CA (1) | CA2304176C (de) |
| DE (1) | DE69721587T2 (de) |
| WO (1) | WO1999014177A1 (de) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB656405A (en) * | 1947-12-09 | 1951-08-22 | Distillers Co Yeast Ltd | Manufacture of methyl-isobutyl ketone |
| US3379766A (en) * | 1964-12-31 | 1968-04-23 | Union Oil Co | Process for the production of higher alkanones from lower alkanones |
| US4704478A (en) * | 1986-06-25 | 1987-11-03 | Union Carbide Corporation | Process for the condensation of ketones |
-
1997
- 1997-09-16 CA CA002304176A patent/CA2304176C/en not_active Expired - Fee Related
- 1997-09-16 AT AT97941628T patent/ATE238980T1/de not_active IP Right Cessation
- 1997-09-16 DE DE69721587T patent/DE69721587T2/de not_active Expired - Fee Related
- 1997-09-16 EP EP97941628A patent/EP1017661B1/de not_active Expired - Lifetime
- 1997-09-16 AU AU43497/97A patent/AU4349797A/en not_active Abandoned
- 1997-09-16 WO PCT/US1997/016340 patent/WO1999014177A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CA2304176A1 (en) | 1999-03-25 |
| CA2304176C (en) | 2004-02-17 |
| EP1017661A1 (de) | 2000-07-12 |
| EP1017661B1 (de) | 2003-05-02 |
| DE69721587D1 (de) | 2003-06-05 |
| DE69721587T2 (de) | 2004-03-25 |
| AU4349797A (en) | 1999-04-05 |
| WO1999014177A1 (en) | 1999-03-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Breen et al. | Mechanistic aspects of the steam reforming of methanol over a CuO/ZnO/ZrO 2/Al 2 O 3 catalyst | |
| Heravi et al. | Wet alumina supported chromium (VI) oxide: A mild, efficient and inexpensive reagent for oxidative deprotection of trimethylsilyl and tetrahydropyranyl ethers in a solventless system | |
| US20040199025A1 (en) | Formaldehyde process | |
| MX172238B (es) | Procedimiento y reactor para generar hidrogeno a partir de hidrocarburos | |
| NO308343B1 (no) | Katalysatorblanding eller reaktantblanding, samt fremgangsmÕte for utførelse av kjemiske reaksjoner | |
| WO2000013783A3 (de) | Mikrostruktur-reaktor | |
| Herrmann et al. | Methyltrioxorhenium: oxidative cleavage of CC-double bonds and its application in a highly efficient synthesis of vanillin from biological waste | |
| KR840001116A (ko) | 촉매적 수소화에 의한 알콜의 제조방법 | |
| Iwahama et al. | Selective oxidation of sulfides to sulfoxides with molecular oxygen catalyzed by N-hydroxyphthalimide (NHPI) in the presence of alcohols | |
| EP0738732A3 (de) | Verfahren zur Herstellung von zyklischen Polysiloxanen | |
| MXPA98008036A (es) | Proceso para la fabricacion de metil mercaptopropanal. | |
| GB1578993A (en) | Dehydrocoupling process | |
| ATE238980T1 (de) | Herstellung von methyl isobutyl und diisobutyl keton | |
| CN104876814B (zh) | 一种阿伏苯宗的合成方法 | |
| JPS5788130A (en) | Preparation of organosiloxane and methyl chloride | |
| CN1800132B (zh) | 芳香烯烃催化氧化制芳香醛 | |
| WO2002022539A3 (en) | Metal molybdate/iron-molybdate dual catalyst bed system and process using the same for methanol oxidation to formaldehyde | |
| MY144289A (en) | Method to make methyl isobutyl ketone and diisobutyl ketone | |
| Dias et al. | Oxidation ofo-Xylene to Phthalic Anhydride over V2O5/TiO2Catalysts: Part 4. Mathematical Modelling Study and Analysis of the Reaction Network | |
| Iwasawa | A Novel Rearrangement of 1-Alkynylcyclopropanol to 2-Cyclopenten-1-one via Dicobalt Hexacarbonyl Complex. | |
| Bowden et al. | Reactions of carbonyl compounds in basic solutions. Part 24. The mechanism of the base-catalysed ring fission of substituted benzocyclobutene-1, 2-diones | |
| KR950011451A (ko) | 하이드리도 카르보닐트리스(트리오가노포스포러스)로듐의 제조방법 | |
| PL182675B1 (pl) | Sposób katalitycznego utleniania węglowodorów izoalkiloaromatycznych | |
| Arai et al. | Evolution and separation of hydrogen in the photolysis of water using titania-coated catalytic palladium membrane reactor | |
| RU96116685A (ru) | Способ получения стирола |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |