ES2026251T3 - Procedimiento para la produccion de ibuprofeno. - Google Patents
Procedimiento para la produccion de ibuprofeno.Info
- Publication number
- ES2026251T3 ES2026251T3 ES198888302410T ES88302410T ES2026251T3 ES 2026251 T3 ES2026251 T3 ES 2026251T3 ES 198888302410 T ES198888302410 T ES 198888302410T ES 88302410 T ES88302410 T ES 88302410T ES 2026251 T3 ES2026251 T3 ES 2026251T3
- Authority
- ES
- Spain
- Prior art keywords
- paladium
- ibpe
- molar
- ions
- water
- 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 - Lifetime
Links
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 229960001680 ibuprofen Drugs 0.000 title 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- CTBUVTVWLYTOGO-UWVJOHFNSA-N 2-[(11z)-11-[3-(dimethylamino)propylidene]-6h-benzo[c][1]benzoxepin-2-yl]acetaldehyde Chemical compound C1OC2=CC=C(CC=O)C=C2C(=C/CCN(C)C)\C2=CC=CC=C21 CTBUVTVWLYTOGO-UWVJOHFNSA-N 0.000 abstract 1
- -1 HYDROGEN IONS Chemical class 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 150000002500 ions Chemical class 0.000 abstract 1
- 239000012074 organic phase Substances 0.000 abstract 1
- 150000002941 palladium compounds Chemical class 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/46—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings and other rings, e.g. cyclohexylphenylacetic acid
- C07C57/50—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings and other rings, e.g. cyclohexylphenylacetic acid containing condensed ring systems
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
- B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
-
- 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
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/12—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/34—Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/824—Palladium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
UN METODO PARA LA PREPARACION DE IBUPROFENO POR CARBONILACION DE 1-(4''-ISOBUTILFENIL) ETANOL (IBPE) CON MONOXIDO DE CARBONO EN UN MEDIO ACUOSO ACIDO, ES DECIR, CONTENIENDO AL MENOS 10% DE AGUA BASADO EN EL PESO DEL IBPE INICIALMENTE AÑADIDO, A UNA TEMPERATURA DE AL MENOS 10 GRADOS C Y UNA PRESION DE MONOXIDO DE CARBONO DE AL MENOS 500 PSIG, Y EN PRESENCIA DE (1) UN CATALIZADOR CONSISTENTE ESENCIALMENTE EN UN COMPUESTO DE PALADIO EN EL QUE EL PALADIO TIENE UNA VALENCIA DE 0 A 2 Y ESTA COMPLEJADO CON AL MENOS UN LIGANDO DE FOSFINA MONODENTADO MISCIBLE CON LA FASE ORGANICA DEL MEDIO DE REACCION, SIENDO LA RELACION MOLAR DE FOSFORO/PALADIO EN DICHO COMPUESTO DE PALADIO Y LIGANDO AL MENOS DE 2:1 CUANDO LA RELACION MOLAR PALADIO/IBPE ESTA POR DEBAJO DE 1:10000; (2) IONES HIDROGENOS DISOCIADOS DE UN ACIDO QUE ES SUSTANCIALMENTE COMPLETAMENTE IONIZABLE EN SOLUCION ACUOSA DISLUIDA TAL QUE LA RELACION MOLAR DE IONES HIDROGENO A IBPE A/ADIDO A LA ZONA DE REACCION ES AL MENOS 0,15 Y LA RELACION MOLAR DE IONES HIDROGENO A AGUA ES AL MEOS 0,026 Y (3) IONES HALURO DISOCIADOS TAL QUE LA RELACION MOLAR DE IONES HALURO A IBPE AÑADIDO ES AL MENOS 0,15
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2851487A | 1987-03-20 | 1987-03-20 | |
| US15814188A | 1988-03-04 | 1988-03-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2026251T3 true ES2026251T3 (es) | 1992-04-16 |
Family
ID=26703780
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES198888302410T Expired - Lifetime ES2026251T3 (es) | 1987-03-20 | 1988-03-18 | Procedimiento para la produccion de ibuprofeno. |
Country Status (22)
| Country | Link |
|---|---|
| EP (1) | EP0284310B1 (es) |
| JP (1) | JPH0686403B2 (es) |
| KR (1) | KR960007822B1 (es) |
| CN (1) | CN1029679C (es) |
| AU (1) | AU620322B2 (es) |
| BR (1) | BR8801238A (es) |
| CA (1) | CA1329396C (es) |
| DE (1) | DE3864713D1 (es) |
| DK (1) | DK148488A (es) |
| ES (1) | ES2026251T3 (es) |
| FI (1) | FI90861C (es) |
| GR (1) | GR3002693T3 (es) |
| HU (1) | HU200983B (es) |
| IE (1) | IE60502B1 (es) |
| IL (1) | IL85736A (es) |
| MX (1) | MX168833B (es) |
| NO (1) | NO169890C (es) |
| NZ (1) | NZ223950A (es) |
| PL (1) | PL153826B1 (es) |
| PT (1) | PT87014B (es) |
| SG (1) | SG22892G (es) |
| YU (1) | YU46539B (es) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4981995A (en) * | 1987-03-20 | 1991-01-01 | Varadaraj Elango | Method for producing ibuprofen |
| CA1338673C (en) * | 1988-04-15 | 1996-10-22 | Graham N. Mott | Catalyst recycle in the carbonylation of isobutylphenylethanol to ibuprofen |
| JP2782080B2 (ja) * | 1989-03-06 | 1998-07-30 | 日本石油化学株式会社 | α―(3―ベンゾイルフェニル)プロピオン酸誘導体の製造方法 |
| HU209123B (en) * | 1990-06-04 | 1994-03-28 | Hoechst Celanese Corp | Process for producing 2-(4'-isobutylphenyl)-propionic acid |
| US5166418A (en) * | 1990-06-04 | 1992-11-24 | Hoechst Celanese Corporation | Method for producing ibuprofen |
| US5179229A (en) * | 1992-04-24 | 1993-01-12 | Hoechst Celanese Corporation | Preparation of 2,2-diorgano-3-arylpropionic acids and esters thereof |
| US5315030A (en) * | 1993-09-29 | 1994-05-24 | Ethyl Corporation | Catalytic carbonylation of ethers and thioethers |
| US5482596A (en) * | 1994-01-27 | 1996-01-09 | Albemarle Corporation | Mixed ligand catalyst for preparing aryl-substituted aliphatic carboxylic esters |
| EP0701987A1 (de) | 1994-09-16 | 1996-03-20 | Cu Chemie Uetikon Ag | Verfahren zur Herstellung von aromatischen Ketonen |
| US6268526B1 (en) | 1998-12-16 | 2001-07-31 | Albemarle Corporation | Palladium catalyzed carbonylation process utilizing aromatic substituted alcohols and/or aromatic substituted alkyl halides |
| CN1309700C (zh) * | 2005-05-27 | 2007-04-11 | 中国科学院上海有机化学研究所 | 一种制备2-芳基乳酸酯及萘普生、布洛芬的方法 |
| CN102329194A (zh) * | 2011-07-15 | 2012-01-25 | 浙江工业大学 | 一种布洛芬中间体对异丁基苯乙醇的制备方法 |
| CN103254070B (zh) * | 2013-02-03 | 2014-11-05 | 青岛科技大学 | 一种由1-(4-异丁基苯基)乙醇制备2-(4-异丁基苯基)丙酸酯的方法 |
| JP7472133B2 (ja) * | 2018-12-03 | 2024-04-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 銅を含む触媒組成物の存在下で1-(4-イソブチルフェニル)エタノンの水素化により1-(4-イソブチルフェニル)エタノールを製造する方法 |
| CN111689847B (zh) * | 2020-06-12 | 2022-05-17 | 浙江新和成股份有限公司 | 芳基丙酸类化合物的制备方法 |
| EP4423045A1 (en) * | 2021-10-28 | 2024-09-04 | Centre National de la Recherche Scientifique | Process for preparing acyl derivatives |
| CN114195633A (zh) * | 2021-12-24 | 2022-03-18 | 浙江新和成股份有限公司 | 一种布洛芬杂质f的合成方法 |
| CN116392986B (zh) * | 2023-06-09 | 2023-08-04 | 北京思达流体科技有限公司 | 1-(4-异丁基苯基)乙醇羰基化的连续化生产系统及操作方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL6702884A (es) * | 1966-03-22 | 1967-09-25 | ||
| SE364254B (es) * | 1967-04-05 | 1974-02-18 | Monsanto Co | |
| JPS5995238A (ja) * | 1982-11-19 | 1984-06-01 | Mitsubishi Petrochem Co Ltd | フエニル酢酸誘導体の製造法 |
| EP0124160B1 (en) * | 1983-05-02 | 1986-09-17 | Shell Internationale Researchmaatschappij B.V. | A process for the preparation of carboxylic acids and/or esters |
-
1988
- 1988-03-14 IL IL85736A patent/IL85736A/xx unknown
- 1988-03-14 CA CA000561404A patent/CA1329396C/en not_active Expired - Fee Related
- 1988-03-18 EP EP88302410A patent/EP0284310B1/en not_active Expired - Lifetime
- 1988-03-18 ES ES198888302410T patent/ES2026251T3/es not_active Expired - Lifetime
- 1988-03-18 DE DE8888302410T patent/DE3864713D1/de not_active Expired - Lifetime
- 1988-03-18 HU HU881366A patent/HU200983B/hu unknown
- 1988-03-18 YU YU55188A patent/YU46539B/sh unknown
- 1988-03-18 PL PL1988271283A patent/PL153826B1/pl unknown
- 1988-03-18 MX MX010825A patent/MX168833B/es unknown
- 1988-03-18 PT PT87014A patent/PT87014B/pt not_active IP Right Cessation
- 1988-03-18 IE IE80088A patent/IE60502B1/en not_active IP Right Cessation
- 1988-03-18 JP JP63063787A patent/JPH0686403B2/ja not_active Expired - Lifetime
- 1988-03-18 DK DK148488A patent/DK148488A/da not_active Application Discontinuation
- 1988-03-18 NO NO881213A patent/NO169890C/no not_active IP Right Cessation
- 1988-03-18 AU AU13284/88A patent/AU620322B2/en not_active Ceased
- 1988-03-18 NZ NZ223950A patent/NZ223950A/xx unknown
- 1988-03-18 BR BR8801238A patent/BR8801238A/pt not_active IP Right Cessation
- 1988-03-18 FI FI881303A patent/FI90861C/fi not_active IP Right Cessation
- 1988-03-19 CN CN88102150A patent/CN1029679C/zh not_active Expired - Lifetime
- 1988-03-19 KR KR1019880002988A patent/KR960007822B1/ko not_active Expired - Fee Related
-
1991
- 1991-09-12 GR GR91400719T patent/GR3002693T3/el unknown
-
1992
- 1992-03-06 SG SG228/92A patent/SG22892G/en unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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