JP2004525918A - モノ−またはビスカルボニル−またはヒドロキシル化合物の製造方法 - Google Patents
モノ−またはビスカルボニル−またはヒドロキシル化合物の製造方法 Download PDFInfo
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- JP2004525918A JP2004525918A JP2002571436A JP2002571436A JP2004525918A JP 2004525918 A JP2004525918 A JP 2004525918A JP 2002571436 A JP2002571436 A JP 2002571436A JP 2002571436 A JP2002571436 A JP 2002571436A JP 2004525918 A JP2004525918 A JP 2004525918A
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- ozone
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- absorber
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- ozonolysis
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- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
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- 229910019142 PO4 Inorganic materials 0.000 description 1
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
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- 239000000919 ceramic Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
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- 230000002950 deficient Effects 0.000 description 1
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- BQHDXNZNSPVVKB-UHFFFAOYSA-N diethyl 2-methylidenepropanedioate Chemical compound CCOC(=O)C(=C)C(=O)OCC BQHDXNZNSPVVKB-UHFFFAOYSA-N 0.000 description 1
- DBKKFIIYQGGHJO-UHFFFAOYSA-N diethyl 2-oxopropanedioate Chemical compound CCOC(=O)C(=O)C(=O)OCC DBKKFIIYQGGHJO-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- APGUUZNLMFETAH-UHFFFAOYSA-N dimethyl cyclohexene-1,2-dicarboxylate Chemical compound COC(=O)C1=C(C(=O)OC)CCCC1 APGUUZNLMFETAH-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- FJAKCEHATXBFJT-UHFFFAOYSA-N ethyl 2-oxobutanoate Chemical compound CCOC(=O)C(=O)CC FJAKCEHATXBFJT-UHFFFAOYSA-N 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
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- 229930195733 hydrocarbon Natural products 0.000 description 1
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- WSZKUEZEYFNPID-UHFFFAOYSA-N hydrogen sulfate;quinolin-1-ium Chemical compound OS(O)(=O)=O.N1=CC=CC2=CC=CC=C21 WSZKUEZEYFNPID-UHFFFAOYSA-N 0.000 description 1
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- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
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- 150000004706 metal oxides Chemical class 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical group C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
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- 238000013021 overheating Methods 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000005440 p-toluyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C(*)=O)C([H])([H])[H] 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
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- 239000010452 phosphate Substances 0.000 description 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 125000000075 primary alcohol group Chemical group 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- BGUWFUQJCDRPTL-UHFFFAOYSA-N pyridine-4-carbaldehyde Chemical compound O=CC1=CC=NC=C1 BGUWFUQJCDRPTL-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229930004725 sesquiterpene Natural products 0.000 description 1
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000011172 small scale experimental method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- UMHFSEWKWORSLP-UHFFFAOYSA-N thiophene 1,1-dioxide Chemical compound O=S1(=O)C=CC=C1 UMHFSEWKWORSLP-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 150000003648 triterpenes Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/48—Aldehydo radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B41/00—Formation or introduction of functional groups containing oxygen
- C07B41/06—Formation or introduction of functional groups containing oxygen of carbonyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C315/00—Preparation of sulfones; Preparation of sulfoxides
- C07C315/04—Preparation of sulfones; Preparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/48—Preparation of compounds having groups
- C07C41/50—Preparation of compounds having groups by reactions producing groups
-
- 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
- C07C45/40—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with ozone; by ozonolysis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/313—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of doubly bound oxygen containing functional groups, e.g. carboxyl groups
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01D—MEASURING NOT SPECIALLY ADAPTED FOR A SPECIFIC VARIABLE; ARRANGEMENTS FOR MEASURING TWO OR MORE VARIABLES NOT COVERED IN A SINGLE OTHER SUBCLASS; TARIFF METERING APPARATUS; MEASURING OR TESTING NOT OTHERWISE PROVIDED FOR
- G01D2205/00—Indexing scheme relating to details of means for transferring or converting the output of a sensing member
- G01D2205/95—Three-dimensional encoders, i.e. having codes extending in three directions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT0037001A AT500489A1 (de) | 2001-03-09 | 2001-03-09 | Verfahren zur herstellung von mono- oder biscarbonyl- oder hydroxylverbindungen |
| PCT/EP2002/001478 WO2002072518A2 (de) | 2001-03-09 | 2002-02-13 | Verfahren zur herstellung von mono- oder biscarbonyl- oder hydroxylverbindungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004525918A true JP2004525918A (ja) | 2004-08-26 |
| JP2004525918A5 JP2004525918A5 (enExample) | 2008-07-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002571436A Pending JP2004525918A (ja) | 2001-03-09 | 2002-02-13 | モノ−またはビスカルボニル−またはヒドロキシル化合物の製造方法 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7169950B2 (enExample) |
| EP (1) | EP1366008B1 (enExample) |
| JP (1) | JP2004525918A (enExample) |
| CN (1) | CN1537087A (enExample) |
| AT (2) | AT500489A1 (enExample) |
| DE (1) | DE50208777D1 (enExample) |
| DK (1) | DK1366008T3 (enExample) |
| ES (1) | ES2275856T3 (enExample) |
| MY (1) | MY129221A (enExample) |
| PT (1) | PT1366008E (enExample) |
| SA (1) | SA02230032B1 (enExample) |
| TW (1) | TWI293625B (enExample) |
| WO (1) | WO2002072518A2 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT2019818T (pt) * | 2006-05-23 | 2020-05-06 | Dpx Holdings Bv | Processo para a produção de compostos por meio de intermediários perigosos numa série de microrreatores |
| WO2010011134A2 (en) * | 2008-07-21 | 2010-01-28 | Dishman Pharmaceuticals And Chemicals Ltd. | Ozonolysis of aromatics and/or olefins |
| EP2399897B1 (en) * | 2009-02-17 | 2015-08-12 | Utsunomiya University | Method for producing oxygen-containing compound |
| MX2018003258A (es) * | 2015-09-20 | 2019-02-07 | Air Cross Inc | Ozonolisis para la activacion de compuestos y degradacion de ozono. |
| CN111333493B (zh) * | 2018-12-18 | 2022-08-05 | 万华化学集团股份有限公司 | 一种二醛半缩醛的制备方法 |
| CN114522683B (zh) * | 2020-11-23 | 2024-04-26 | 中国科学院大连化学物理研究所 | 一种碳载Pd-M双金属单原子催化剂及其在C2H2双羰基化反应中应用 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2813113A (en) * | 1953-05-07 | 1957-11-12 | Emery Industries Inc | Method of making azelaic acid |
| US3507793A (en) * | 1964-10-01 | 1970-04-21 | Ethyl Corp | Preparation of carboxylic acid-ketone mixtures |
| DE2514001A1 (de) * | 1975-03-29 | 1976-10-07 | Basf Ag | Verfahren zur herstellung von glyoxalmonoacetalen |
| DE2713863A1 (de) * | 1977-03-29 | 1978-10-12 | Henkel Kgaa | Verfahren und vorrichtung zum kontinuierlichen ozonisieren |
| DE2754366A1 (de) * | 1977-12-07 | 1979-06-13 | Henkel Kgaa | Vorrichtung zum kontinuierlichen ozonisieren |
| AT380008B (de) * | 1983-12-23 | 1986-03-25 | Chemie Linz Ag | Verfahren zur herstellung von mono- oder biscarbonylverbindungen |
| EP0555472B1 (en) * | 1991-08-06 | 1995-11-29 | Lion Corporation | Process for ozonizing unsaturated fatty acid or lower alkyl ester thereof and oxidative decomposition of the resulting ozonide |
| JPH05140030A (ja) * | 1991-11-19 | 1993-06-08 | Agency Of Ind Science & Technol | グリオキシル酸類の製造方法 |
| JPH09124553A (ja) * | 1995-10-27 | 1997-05-13 | Tonen Corp | グリオキシル酸エチルの製造方法 |
| EP1095700A1 (de) * | 1999-10-29 | 2001-05-02 | Dr. Frische GmbH | Verfahren zur Durchführung einer Mehrphasenreaktion nach dem Gegenstromprinzip einer flüssigen und gasförmigen Phase und Vorrichtung zur Durchführung des Verfahrens |
-
2001
- 2001-03-09 AT AT0037001A patent/AT500489A1/de not_active Application Discontinuation
-
2002
- 2002-02-13 DE DE50208777T patent/DE50208777D1/de not_active Withdrawn - After Issue
- 2002-02-13 AT AT02719815T patent/ATE346032T1/de not_active IP Right Cessation
- 2002-02-13 PT PT02719815T patent/PT1366008E/pt unknown
- 2002-02-13 JP JP2002571436A patent/JP2004525918A/ja active Pending
- 2002-02-13 WO PCT/EP2002/001478 patent/WO2002072518A2/de not_active Ceased
- 2002-02-13 ES ES02719815T patent/ES2275856T3/es not_active Expired - Lifetime
- 2002-02-13 CN CNA028062450A patent/CN1537087A/zh active Pending
- 2002-02-13 EP EP02719815A patent/EP1366008B1/de not_active Expired - Lifetime
- 2002-02-13 US US10/469,306 patent/US7169950B2/en not_active Expired - Fee Related
- 2002-02-13 DK DK02719815T patent/DK1366008T3/da active
- 2002-02-22 MY MYPI20020609A patent/MY129221A/en unknown
- 2002-02-25 TW TW091103343A patent/TWI293625B/zh active
- 2002-03-31 SA SA2230032A patent/SA02230032B1/ar unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MY129221A (en) | 2007-03-30 |
| AT500489A1 (de) | 2006-01-15 |
| ES2275856T3 (es) | 2007-06-16 |
| ATE346032T1 (de) | 2006-12-15 |
| WO2002072518A3 (de) | 2002-11-28 |
| US7169950B2 (en) | 2007-01-30 |
| WO2002072518A2 (de) | 2002-09-19 |
| EP1366008A2 (de) | 2003-12-03 |
| US20040073041A1 (en) | 2004-04-15 |
| DK1366008T3 (da) | 2007-02-19 |
| TWI293625B (en) | 2008-02-21 |
| EP1366008B1 (de) | 2006-11-22 |
| DE50208777D1 (de) | 2007-01-04 |
| CN1537087A (zh) | 2004-10-13 |
| SA02230032B1 (ar) | 2008-07-19 |
| PT1366008E (pt) | 2007-02-28 |
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