ES2698849T3 - Procedimiento para la preparación de ciclododecanona pura - Google Patents
Procedimiento para la preparación de ciclododecanona pura Download PDFInfo
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- ES2698849T3 ES2698849T3 ES10701244T ES10701244T ES2698849T3 ES 2698849 T3 ES2698849 T3 ES 2698849T3 ES 10701244 T ES10701244 T ES 10701244T ES 10701244 T ES10701244 T ES 10701244T ES 2698849 T3 ES2698849 T3 ES 2698849T3
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- 238000000034 method Methods 0.000 title claims abstract description 133
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- SXVPOSFURRDKBO-UHFFFAOYSA-N Cyclododecanone Chemical compound O=C1CCCCCCCCCCC1 SXVPOSFURRDKBO-UHFFFAOYSA-N 0.000 title description 44
- 239000000203 mixture Substances 0.000 claims abstract description 220
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 195
- 239000003054 catalyst Substances 0.000 claims abstract description 116
- 230000008569 process Effects 0.000 claims abstract description 103
- 150000001923 cyclic compounds Chemical class 0.000 claims abstract description 101
- 125000000468 ketone group Chemical group 0.000 claims abstract description 100
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 claims abstract description 97
- 150000001875 compounds Chemical class 0.000 claims abstract description 86
- 238000004821 distillation Methods 0.000 claims abstract description 80
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 57
- -1 cyclic olefin Chemical class 0.000 claims abstract description 53
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 52
- 238000011282 treatment Methods 0.000 claims abstract description 52
- 235000013842 nitrous oxide Nutrition 0.000 claims abstract description 49
- 125000003172 aldehyde group Chemical group 0.000 claims abstract description 48
- 229960001730 nitrous oxide Drugs 0.000 claims abstract description 47
- 238000000926 separation method Methods 0.000 claims abstract description 45
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 37
- 230000003647 oxidation Effects 0.000 claims abstract description 35
- ZOLLIQAKMYWTBR-RYMQXAEESA-N cyclododecatriene Chemical compound C/1C\C=C\CC\C=C/CC\C=C\1 ZOLLIQAKMYWTBR-RYMQXAEESA-N 0.000 claims abstract description 28
- QCSDLMPAQMQZOE-QSWGICILSA-N (1z,9z)-cyclohexadeca-1,9-diene Chemical compound C1CCC\C=C/CCCCCC\C=C/CC1 QCSDLMPAQMQZOE-QSWGICILSA-N 0.000 claims abstract description 7
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000004912 1,5-cyclooctadiene Substances 0.000 claims abstract description 7
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 claims abstract description 6
- KEMUGHMYINTXKW-NQOXHWNZSA-N (1z,5z)-cyclododeca-1,5-diene Chemical compound C1CCC\C=C/CC\C=C/CC1 KEMUGHMYINTXKW-NQOXHWNZSA-N 0.000 claims abstract description 5
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 claims abstract description 5
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- 238000002425 crystallisation Methods 0.000 claims description 13
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- OAROPPDXVNGIBY-UHFFFAOYSA-N 5-ethylidene-1,7,7-trimethylbicyclo[2.2.1]hept-2-ene Chemical compound C(C)=C1C2C=CC(C1)(C2(C)C)C OAROPPDXVNGIBY-UHFFFAOYSA-N 0.000 abstract 1
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- ZOLLIQAKMYWTBR-FFWAUJBHSA-N (1e,5e,9e)-cyclododeca-1,5,9-triene Chemical compound C/1C\C=C\CC\C=C\CC\C=C\1 ZOLLIQAKMYWTBR-FFWAUJBHSA-N 0.000 description 20
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- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 11
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 11
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 9
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- 239000002815 homogeneous catalyst Substances 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 229920006395 saturated elastomer Polymers 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 150000001336 alkenes Chemical class 0.000 description 7
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- 229910052707 ruthenium Inorganic materials 0.000 description 7
- 229910052719 titanium Inorganic materials 0.000 description 7
- 239000010936 titanium Substances 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 125000005594 diketone group Chemical class 0.000 description 6
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical class [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 5
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 5
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- 239000003085 diluting agent Substances 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 229910052763 palladium Inorganic materials 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 4
- BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
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- ZSWOXZQJIPGJEY-UHFFFAOYSA-N cyclododeca-2,4-dien-1-one Chemical compound O=C1CCCCCCCC=CC=C1 ZSWOXZQJIPGJEY-UHFFFAOYSA-N 0.000 description 4
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- 229910052742 iron Inorganic materials 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
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- RDAFFINKUCJOJK-MPQNWDQLSA-N (5e)-cyclodeca-1,5-diene Chemical compound C1CC\C=C\CCC=CC1 RDAFFINKUCJOJK-MPQNWDQLSA-N 0.000 description 1
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- 238000005575 aldol reaction Methods 0.000 description 1
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- 239000003513 alkali Substances 0.000 description 1
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- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
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- 238000001354 calcination Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
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- GWCMUONZBWHLRN-UHFFFAOYSA-N cyclodeca-1,6-diene Chemical compound C1CC=CCCCC=CC1 GWCMUONZBWHLRN-UHFFFAOYSA-N 0.000 description 1
- SXOZDDAFVJANJP-UHFFFAOYSA-N cyclodecanone Chemical compound O=C1CCCCCCCCC1 SXOZDDAFVJANJP-UHFFFAOYSA-N 0.000 description 1
- KEMUGHMYINTXKW-UHFFFAOYSA-N cyclododeca-1,5-diene Chemical compound C1CCCC=CCCC=CCC1 KEMUGHMYINTXKW-UHFFFAOYSA-N 0.000 description 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
- HSXHQSIOZSTGKP-UHFFFAOYSA-N cyclohexadeca-1,5,9,13-tetraene Chemical compound C1CC=CCCC=CCCC=CCCC=C1 HSXHQSIOZSTGKP-UHFFFAOYSA-N 0.000 description 1
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- SIYBPTIIYPOCTE-UHFFFAOYSA-N dodeca-4,8,11-trienal Chemical class C=CCC=CCCC=CCCC=O SIYBPTIIYPOCTE-UHFFFAOYSA-N 0.000 description 1
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- 150000004677 hydrates Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
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- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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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
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C07C45/82—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
-
- 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
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/28—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of CHx-moieties
-
- 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
- C07C45/62—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 hydrogenation of carbon-to-carbon double or triple bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/18—Systems containing only non-condensed rings with a ring being at least seven-membered
- C07C2601/20—Systems containing only non-condensed rings with a ring being at least seven-membered the ring being twelve-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
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|---|---|---|---|
| EP09151525 | 2009-01-28 | ||
| PCT/EP2010/050888 WO2010086314A1 (de) | 2009-01-28 | 2010-01-27 | Verfahren zur herstellung von reinem cyclododecanon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2698849T3 true ES2698849T3 (es) | 2019-02-06 |
Family
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|---|---|---|---|
| ES10701244T Active ES2698849T3 (es) | 2009-01-28 | 2010-01-27 | Procedimiento para la preparación de ciclododecanona pura |
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|---|---|
| US (1) | US8188320B2 (https=) |
| EP (1) | EP2391597B1 (https=) |
| JP (1) | JP5661647B2 (https=) |
| KR (1) | KR20110110359A (https=) |
| CN (1) | CN102365256A (https=) |
| ES (1) | ES2698849T3 (https=) |
| WO (1) | WO2010086314A1 (https=) |
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| US8188320B2 (en) | 2009-01-28 | 2012-05-29 | Basf Se | Process for preparing pure cyclododecanone |
| DE102009047196A1 (de) | 2009-11-26 | 2011-06-01 | Basf Se | Verfahren zur Herstellung von 1,6-Hexandiol |
| JP5708637B2 (ja) | 2010-03-15 | 2015-04-30 | 宇部興産株式会社 | アミド化合物の製造方法 |
| US9394212B2 (en) | 2010-06-15 | 2016-07-19 | Basf Se | Process for the cooligomerization of olefins |
| US8940940B2 (en) | 2012-06-13 | 2015-01-27 | Basf Se | Process for preparing macrocyclic ketones |
| DE102014212602A1 (de) | 2013-07-02 | 2015-01-08 | Basf Se | Verfahren zur Herstellung eines Ketons aus einem Olefin |
| EP2980069A1 (de) * | 2014-08-01 | 2016-02-03 | Evonik Degussa GmbH | Verfahren zur Herstellung von Cyclododecanon |
| EP3002003A1 (de) * | 2014-09-30 | 2016-04-06 | Basf Se | Verwendung neuartiger cyclischer Carbaldehyde als Aromastoff |
| EP3002058A1 (de) * | 2014-10-02 | 2016-04-06 | Evonik Degussa GmbH | Katalysatorsystem zur Herstellung von Ketonen aus Epoxiden |
| WO2016059042A1 (de) * | 2014-10-14 | 2016-04-21 | Basf Se | Verwendung von hexadeca-8,15-dienal als aromachemikalie |
| EP3050869B1 (de) * | 2015-01-30 | 2019-10-02 | Symrise AG | Verfahren zur Herstellung von substituierten Alkylcycloalkanonen |
| EP3153493A1 (de) * | 2015-10-08 | 2017-04-12 | Basf Se | Verfahren zur reinigung von cyclohexadec-8-en-1-on |
| EP3359516A1 (de) * | 2015-10-08 | 2018-08-15 | Basf Se | Verwendung neuartiger gemische von (e/z)-cyclopentadecenon-isomeren, deren herstellung und deren verwendung als aromastoff |
| WO2020187733A1 (en) * | 2019-03-15 | 2020-09-24 | Basf Se | Use of 4,8,11-dodecatrienal to impart a clean aroma impression to a composition. |
| CN114874085B (zh) * | 2022-07-12 | 2022-10-11 | 中国天辰工程有限公司 | 一种环十二酮提纯工艺 |
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| US316917A (en) | 1885-04-28 | Cord-spool and tension device for grain-binders | ||
| US2875256A (en) | 1953-01-21 | 1959-02-24 | Shell Dev | Dienic hydrocarbons and derivatives thereof |
| DE1283836B (de) | 1959-12-22 | 1968-11-28 | Studiengesellschaft Kohle Mbh | Verfahren zur Herstellung von hauptsaechlich Cyclododekatrien-(1,5,9) enthaltenden Produkten durch Cyclooligomerisation von 1, 3-Diolefinen |
| US3182093A (en) | 1961-10-02 | 1965-05-04 | Exxon Research Engineering Co | Preparation of 1, 5-cyclododecadiene |
| BE646244A (https=) | 1963-04-10 | 1900-01-01 | ||
| US3804914A (en) | 1972-05-25 | 1974-04-16 | Phillips Petroleum Co | Ruthenium(ii)complexes as catalysts for selective hydrogenation of cyclic polyenes to cyclic monoenes |
| DD115480A2 (https=) | 1974-08-19 | 1975-10-05 | ||
| DE2519817A1 (de) | 1975-05-03 | 1976-11-11 | Hoechst Ag | Verfahren zur herstellung von butandiol-(1.4) |
| US4658065A (en) | 1984-03-28 | 1987-04-14 | Asahi Kasei Kogyo Kabushiki Kaisha | Process for producing polyether polyol and a product |
| EP0279397B1 (en) | 1987-02-16 | 1991-06-12 | Sumitomo Chemical Company, Limited | Solid base, process for preparing the same and use of the same in preparation of internal olefins |
| GB8707595D0 (en) | 1987-03-31 | 1987-05-07 | British Petroleum Co Plc | Chemical process |
| US5128296A (en) | 1991-07-01 | 1992-07-07 | Phillips Petroleum Company | Selective hydrogenation of cyclic polyenes |
| US5210349A (en) | 1991-07-01 | 1993-05-11 | Phillips Petroleum Company | Selective hydrogenation of cyclic polyenes |
| US5180870A (en) | 1991-10-23 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Hydrogenation of polyenes |
| US5177278A (en) | 1991-10-23 | 1993-01-05 | E. I. Du Pont De Nemours And Company | Preparation of cyclododecene |
| US5321176A (en) | 1992-12-22 | 1994-06-14 | E. I. Du Pont De Nemours And Company | Hydrogenation of polyenes |
| DE19510993C1 (de) | 1995-03-24 | 1996-08-29 | Fhw Brenntechnik Gmbh | Vorrichtung zur thermischen Abgasbehandlung, insbesondere von oxidierbaren Schwelgasen |
| EP0915100A4 (en) | 1996-12-05 | 2002-10-09 | Kyowa Hakko Kogyo Kk | NEW PROTEIN |
| DE10142033A1 (de) | 2001-08-28 | 2003-03-20 | Haarmann & Reimer Gmbh | Metathesekatalysatoren |
| DE10344595A1 (de) | 2003-09-25 | 2005-05-12 | Basf Ag | Verfahren zur Herstellung eines Ketons |
| DE102004046167A1 (de) | 2004-09-23 | 2006-04-06 | Basf Ag | Verfahren zur Reinigung und Aufkonzentrierung von Distickstoffmonoxid |
| DE102005048250A1 (de) * | 2005-10-07 | 2007-04-12 | Basf Ag | Verfahren zur Farbzahlverbesserung |
| DE102005055588A1 (de) | 2005-11-22 | 2007-05-24 | Basf Ag | Verfahren zur Isolierung von N2O |
| WO2007104650A1 (de) | 2006-03-10 | 2007-09-20 | Basf Se | Verfahren zur herstellung von benzophenoniminen |
| ES2346098T3 (es) | 2006-06-29 | 2010-10-08 | Basf Se | Procedimiento para la obtencion de cetonas ciclicas. |
| DE502007002353D1 (de) | 2006-06-29 | 2010-01-28 | Basf Se | Verfahren zur herstellung von cyclischen ketonen |
| ES2417180T3 (es) | 2006-06-29 | 2013-08-06 | Basf Se | Purificación de ciclododecanona mediante tratamiento térmico |
| JP5244121B2 (ja) | 2006-12-11 | 2013-07-24 | ビーエーエスエフ ソシエタス・ヨーロピア | Ｎ２ｏを単離する方法 |
| EP2190806A2 (de) | 2007-08-21 | 2010-06-02 | Basf Se | Verfahren und vorrichtung zur oxidation organischer verbindungen |
| JP5733979B2 (ja) | 2007-08-21 | 2015-06-10 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 有機化合物を酸化するための方法および装置 |
| CN101903368A (zh) | 2007-12-21 | 2010-12-01 | 巴斯夫欧洲公司 | 制备ε-己内酯的方法 |
| DE112009000169B4 (de) | 2008-01-25 | 2021-07-29 | Basf Se | Methode zur selektiven großtechnischen Herstellung von 1,5,9 Cyclododecatrien |
| WO2009092682A2 (de) | 2008-01-25 | 2009-07-30 | Basf Se | Verfahren und vorrichtung zur destillativen aufarbeitung von 1,5,9-cyclododecatrien und gewinnung von cdt mit hoher reinheit |
| BRPI0910974B1 (pt) | 2008-04-02 | 2019-12-31 | Basf Se | processo para purificar uma mistura gasosa |
| US8404901B2 (en) | 2008-04-02 | 2013-03-26 | Basf Se | Process for purifying dinitrogen monoxide |
| CN104761438A (zh) | 2008-08-29 | 2015-07-08 | 巴斯夫欧洲公司 | 制备环酮的方法 |
| EP2384317B1 (de) | 2008-12-30 | 2014-04-23 | Basf Se | Verfahren zur herstellung von ketonen durch umsetzung von 1,1-disubtituierten olefinen mit n2o |
| JP5656872B2 (ja) | 2009-01-21 | 2015-01-21 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 非触媒作用又は均一系触媒作用反応のための管束反応器 |
| US8188320B2 (en) | 2009-01-28 | 2012-05-29 | Basf Se | Process for preparing pure cyclododecanone |
| US8212082B2 (en) | 2009-01-28 | 2012-07-03 | Basf Se | Process for the isolation of dodecatrienal and its use as aroma substance |
-
2010
- 2010-01-27 US US12/694,815 patent/US8188320B2/en not_active Expired - Fee Related
- 2010-01-27 JP JP2011546824A patent/JP5661647B2/ja not_active Expired - Fee Related
- 2010-01-27 KR KR1020117019844A patent/KR20110110359A/ko not_active Abandoned
- 2010-01-27 CN CN2010800147909A patent/CN102365256A/zh active Pending
- 2010-01-27 WO PCT/EP2010/050888 patent/WO2010086314A1/de not_active Ceased
- 2010-01-27 EP EP10701244.5A patent/EP2391597B1/de active Active
- 2010-01-27 ES ES10701244T patent/ES2698849T3/es active Active
Also Published As
| Publication number | Publication date |
|---|---|
| KR20110110359A (ko) | 2011-10-06 |
| WO2010086314A1 (de) | 2010-08-05 |
| EP2391597A1 (de) | 2011-12-07 |
| CN102365256A (zh) | 2012-02-29 |
| US8188320B2 (en) | 2012-05-29 |
| US20100191018A1 (en) | 2010-07-29 |
| JP2012516301A (ja) | 2012-07-19 |
| EP2391597B1 (de) | 2018-08-22 |
| JP5661647B2 (ja) | 2015-01-28 |
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