KR20100043253A - 유기 화합물의 산화를 위한 방법 및 장치 - Google Patents
유기 화합물의 산화를 위한 방법 및 장치 Download PDFInfo
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- KR20100043253A KR20100043253A KR1020107003655A KR20107003655A KR20100043253A KR 20100043253 A KR20100043253 A KR 20100043253A KR 1020107003655 A KR1020107003655 A KR 1020107003655A KR 20107003655 A KR20107003655 A KR 20107003655A KR 20100043253 A KR20100043253 A KR 20100043253A
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- South Korea
- Prior art keywords
- reaction zone
- reactor
- reaction
- isothermal
- oxygen
- Prior art date
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- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 37
- 238000000034 method Methods 0.000 title claims abstract description 36
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- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- QRMPKOFEUHIBNM-UHFFFAOYSA-N p-dimethylcyclohexane Natural products CC1CCC(C)CC1 QRMPKOFEUHIBNM-UHFFFAOYSA-N 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- DUCKXCGALKOSJF-UHFFFAOYSA-N pentanoyl pentanoate Chemical compound CCCCC(=O)OC(=O)CCCC DUCKXCGALKOSJF-UHFFFAOYSA-N 0.000 description 1
- FGPPDYNPZTUNIU-UHFFFAOYSA-N pentyl pentanoate Chemical compound CCCCCOC(=O)CCCC FGPPDYNPZTUNIU-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- RUPAXCPQAAOIPB-UHFFFAOYSA-N tert-butyl formate Chemical compound CC(C)(C)OC=O RUPAXCPQAAOIPB-UHFFFAOYSA-N 0.000 description 1
- FLTJDUOFAQWHDF-UHFFFAOYSA-N trimethyl pentane Natural products CCCCC(C)(C)C FLTJDUOFAQWHDF-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/23—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
- C07C51/235—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07114711 | 2007-08-21 | ||
| EP07114711.0 | 2007-08-21 |
Publications (1)
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| KR20100043253A true KR20100043253A (ko) | 2010-04-28 |
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| EP (1) | EP2190805B1 (enExample) |
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| CN (1) | CN101784511B (enExample) |
| BR (1) | BRPI0815629B8 (enExample) |
| MY (1) | MY155650A (enExample) |
| WO (1) | WO2009024446A2 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102008041652A1 (de) | 2008-08-28 | 2010-03-04 | Evonik Oxeno Gmbh | Vorrichtung und Verfahren für die kontinuierliche Umsetzung einer Flüssigkeit mit einem Gas |
| EP2384317B1 (de) | 2008-12-30 | 2014-04-23 | Basf Se | Verfahren zur herstellung von ketonen durch umsetzung von 1,1-disubtituierten olefinen mit n2o |
| JP5661647B2 (ja) * | 2009-01-28 | 2015-01-28 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 純粋なシクロドデカノンの製法 |
| DE102009027978A1 (de) * | 2009-07-23 | 2011-01-27 | Evonik Oxeno Gmbh | Verfahren zur Herstellung von Decancarbonsäuren |
| FR2975393B1 (fr) * | 2011-05-19 | 2013-05-10 | Rhodia Operations | Procede d'hydroxylation de phenols et d'ethers de phenols |
| CN110526814A (zh) * | 2019-07-27 | 2019-12-03 | 宁夏沃凯珑新材料有限公司 | 连续化制备丁酸的方法 |
| JP7676412B2 (ja) | 2020-01-09 | 2025-05-14 | ビーエーエスエフ ソシエタス・ヨーロピア | C3~5飽和脂肪族カルボン酸の調製のための方法 |
| JP7735389B2 (ja) | 2020-08-20 | 2025-09-08 | ビーエーエスエフ ソシエタス・ヨーロピア | C6~12飽和脂肪族カルボン酸の調製のための方法 |
| CN114149313B (zh) * | 2022-02-09 | 2022-04-15 | 山东亿科化学有限责任公司 | 一种制备异壬酸的方法 |
| CN114984897B (zh) * | 2022-05-20 | 2023-10-17 | 万华化学集团股份有限公司 | 一种氧化-过氧化物分解耦合反应装置及其用于有机醛氧化生产有机酸的方法 |
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|---|---|---|---|---|
| EP0733401B1 (de) | 1995-03-24 | 2001-12-05 | Basf Aktiengesellschaft | Verfahren zur Durchführung von Gas/Flüssigreaktionen unter Vermeidung einer zusammenhängenden Gasphase |
| US6362367B2 (en) * | 1998-04-21 | 2002-03-26 | Union Carbide Chemicals & Plastics Technology Corp. | Preparation of organic acids |
| DE19835907A1 (de) | 1998-08-07 | 2000-02-17 | Basf Ag | Verfahren zur Umsetzung einer organischen Verbindung mit einem Hydroperoxid |
| DE19854637A1 (de) | 1998-11-26 | 2000-05-31 | Basf Ag | Reaktor zur kontinuierlichen Durchführung von Gas-Flüssig-, Flüssig-Flüssig- oder Gas-Flüssig-Fest-Reaktionen |
| CN1231444C (zh) | 1999-12-22 | 2005-12-14 | 国际人造丝公司 | 氧化方法 |
| DE10010769C1 (de) | 2000-03-04 | 2001-10-31 | Celanese Chem Europe Gmbh | Nichtkatalytisches Verfahren zur Herstellung aliphatischer Carbonsäuren durch Oxidation in mindestens zwei Stufen von Aldehyden |
| DE102004021763A1 (de) | 2004-04-30 | 2005-05-25 | Basf Ag | Verfahren zum Langzeitbetrieb einer heterogen katalysierten Gasphasenpartialoxidation von Acrolein zu Acrylsäure |
| US7741515B2 (en) * | 2004-09-02 | 2010-06-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
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2008
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- 2008-08-01 WO PCT/EP2008/060121 patent/WO2009024446A2/de not_active Ceased
- 2008-08-01 MY MYPI2010000689A patent/MY155650A/en unknown
- 2008-08-01 EP EP08786741.2A patent/EP2190805B1/de not_active Not-in-force
- 2008-08-01 BR BRPI0815629A patent/BRPI0815629B8/pt not_active IP Right Cessation
- 2008-08-01 US US12/674,058 patent/US8575379B2/en not_active Expired - Fee Related
- 2008-08-01 KR KR1020107003655A patent/KR20100043253A/ko not_active Ceased
- 2008-08-01 JP JP2010521381A patent/JP5733979B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN101784511B (zh) | 2014-11-05 |
| JP2010536816A (ja) | 2010-12-02 |
| CN101784511A (zh) | 2010-07-21 |
| EP2190805A2 (de) | 2010-06-02 |
| JP5733979B2 (ja) | 2015-06-10 |
| BRPI0815629A2 (pt) | 2015-02-18 |
| BRPI0815629B8 (pt) | 2017-04-04 |
| WO2009024446A2 (de) | 2009-02-26 |
| MY155650A (en) | 2015-11-13 |
| US8575379B2 (en) | 2013-11-05 |
| BRPI0815629B1 (pt) | 2017-03-14 |
| US20110087038A1 (en) | 2011-04-14 |
| WO2009024446A3 (de) | 2009-05-07 |
| EP2190805B1 (de) | 2016-02-17 |
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