RU2220129C2 - Способ получения уксусной кислоты и/или метилацетата в присутствии иридия и платины - Google Patents
Способ получения уксусной кислоты и/или метилацетата в присутствии иридия и платины Download PDFInfo
- Publication number
- RU2220129C2 RU2220129C2 RU2001111864/04A RU2001111864A RU2220129C2 RU 2220129 C2 RU2220129 C2 RU 2220129C2 RU 2001111864/04 A RU2001111864/04 A RU 2001111864/04A RU 2001111864 A RU2001111864 A RU 2001111864A RU 2220129 C2 RU2220129 C2 RU 2220129C2
- Authority
- RU
- Russia
- Prior art keywords
- platinum
- iridium
- maintained
- carbon monoxide
- reaction medium
- Prior art date
Links
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 title claims abstract 43
- 238000000034 method Methods 0.000 title claims abstract 30
- 229910052697 platinum Inorganic materials 0.000 title claims abstract 21
- 229910052741 iridium Inorganic materials 0.000 title claims abstract 12
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 title claims abstract 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 title claims abstract 9
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 title claims abstract 3
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 title claims abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract 18
- 239000012429 reaction media Substances 0.000 claims abstract 12
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract 11
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract 11
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims abstract 10
- 230000003197 catalytic effect Effects 0.000 claims abstract 9
- 238000005810 carbonylation reaction Methods 0.000 claims abstract 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract 6
- 230000006315 carbonylation Effects 0.000 claims abstract 5
- 150000004696 coordination complex Chemical class 0.000 claims abstract 5
- 229910052736 halogen Inorganic materials 0.000 claims abstract 5
- 150000002367 halogens Chemical class 0.000 claims abstract 5
- 238000006317 isomerization reaction Methods 0.000 claims abstract 5
- 239000003446 ligand Substances 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- 239000007791 liquid phase Substances 0.000 claims abstract 2
- 150000002903 organophosphorus compounds Chemical class 0.000 claims abstract 2
- 239000002904 solvent Substances 0.000 claims abstract 2
- 229910052703 rhodium Inorganic materials 0.000 claims 5
- 239000010948 rhodium Substances 0.000 claims 5
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims 5
- 238000006243 chemical reaction Methods 0.000 claims 4
- 229910052751 metal Inorganic materials 0.000 claims 4
- 239000002184 metal Substances 0.000 claims 4
- 150000004694 iodide salts Chemical class 0.000 claims 2
- 239000011541 reaction mixture Substances 0.000 claims 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical group IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- 229910017464 nitrogen compound Inorganic materials 0.000 claims 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 claims 1
- 229910003446 platinum oxide Inorganic materials 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 1
- -1 or organonitrogen Chemical class 0.000 abstract 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/12—Acetic acid esters
- C07C69/14—Acetic acid esters of monohydroxylic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/353—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/36—Preparation of carboxylic acid esters by reaction with carbon monoxide or formates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR98/13954 | 1998-11-05 | ||
| FR9813954A FR2785606B1 (fr) | 1998-11-05 | 1998-11-05 | Preparation d'acide acetique et/ou d'acetate de methyle en presence d'iridium et de platine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2001111864A RU2001111864A (ru) | 2003-05-20 |
| RU2220129C2 true RU2220129C2 (ru) | 2003-12-27 |
Family
ID=9532421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2001111864/04A RU2220129C2 (ru) | 1998-11-05 | 1999-10-29 | Способ получения уксусной кислоты и/или метилацетата в присутствии иридия и платины |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6916952B1 (enExample) |
| EP (1) | EP1127042B1 (enExample) |
| JP (1) | JP4066305B2 (enExample) |
| KR (1) | KR100687510B1 (enExample) |
| CN (1) | CN1216845C (enExample) |
| AT (1) | ATE245619T1 (enExample) |
| AU (1) | AU6348499A (enExample) |
| CA (1) | CA2348472C (enExample) |
| DE (1) | DE69909816T2 (enExample) |
| ES (1) | ES2205888T3 (enExample) |
| FR (1) | FR2785606B1 (enExample) |
| ID (1) | ID28477A (enExample) |
| MY (1) | MY121111A (enExample) |
| RU (1) | RU2220129C2 (enExample) |
| TW (1) | TW522146B (enExample) |
| UA (1) | UA68398C2 (enExample) |
| WO (1) | WO2000027785A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2820422B1 (fr) * | 2001-02-08 | 2003-04-25 | Acetex Chimie | Modification du systeme catalytique dans un procede industriel de fabrication d'acide acetique et/ou d'acetate de methyle |
| CA2496839A1 (en) | 2004-07-19 | 2006-01-19 | Woodland Chemical Systems Inc. | Process for producing ethanol from synthesis gas rich in carbon monoxide |
| AU2007235322A1 (en) * | 2006-04-05 | 2007-10-18 | Woodland Biofuels Inc. | System and method for converting biomass to ethanol via syngas |
| CN102442897B (zh) * | 2010-10-13 | 2014-05-28 | 中国石油化工股份有限公司 | 一种羰基化反应制备乙酸的方法 |
| CN102366724B (zh) * | 2011-12-01 | 2013-05-15 | 重庆大学 | 一种甲醇羰基化合成醋酸的催化剂体系及应用 |
| CN110642698A (zh) * | 2019-10-31 | 2020-01-03 | 江苏润普食品科技股份有限公司 | 山梨酸聚酯酸解制备山梨酸的生产方法 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1234641A (enExample) * | 1967-04-05 | 1971-06-09 | ||
| SU1416053A3 (ru) * | 1984-05-03 | 1988-08-07 | Силаниз Корпорейшн (Фирма) | Способ получени уксусной кислоты |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2746795B1 (fr) * | 1996-03-27 | 1998-06-19 | Rhone Poulenc Chimie | Procede de preparation d'acide acetique et/ou d'acetate de methyle par isomerisation et carbonylation |
| FR2750985B1 (fr) * | 1996-07-10 | 1998-11-06 | Rhone Poulenc Chimie | Procede de preparation d'acide acetique et/ou d'acetate de methyle par carbonylation en presence d'iridium et de rhodium |
| US5900505A (en) * | 1997-02-04 | 1999-05-04 | Eastman Chemical Company | Heterogeneous vapor phase carbonylation process |
-
1998
- 1998-11-05 FR FR9813954A patent/FR2785606B1/fr not_active Expired - Fee Related
-
1999
- 1999-10-29 ES ES99950883T patent/ES2205888T3/es not_active Expired - Lifetime
- 1999-10-29 RU RU2001111864/04A patent/RU2220129C2/ru not_active IP Right Cessation
- 1999-10-29 JP JP2000580967A patent/JP4066305B2/ja not_active Expired - Fee Related
- 1999-10-29 AU AU63484/99A patent/AU6348499A/en not_active Abandoned
- 1999-10-29 EP EP99950883A patent/EP1127042B1/fr not_active Expired - Lifetime
- 1999-10-29 ID IDW00200100993A patent/ID28477A/id unknown
- 1999-10-29 KR KR1020017005479A patent/KR100687510B1/ko not_active Expired - Fee Related
- 1999-10-29 CN CN998128880A patent/CN1216845C/zh not_active Expired - Fee Related
- 1999-10-29 WO PCT/FR1999/002652 patent/WO2000027785A1/fr not_active Ceased
- 1999-10-29 CA CA002348472A patent/CA2348472C/en not_active Expired - Fee Related
- 1999-10-29 US US09/807,434 patent/US6916952B1/en not_active Expired - Lifetime
- 1999-10-29 DE DE69909816T patent/DE69909816T2/de not_active Expired - Lifetime
- 1999-10-29 UA UA2001053084A patent/UA68398C2/uk unknown
- 1999-10-29 AT AT99950883T patent/ATE245619T1/de not_active IP Right Cessation
- 1999-11-03 MY MYPI99004766A patent/MY121111A/en unknown
- 1999-11-05 TW TW088119347A patent/TW522146B/zh not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1234641A (enExample) * | 1967-04-05 | 1971-06-09 | ||
| SU1416053A3 (ru) * | 1984-05-03 | 1988-08-07 | Силаниз Корпорейшн (Фирма) | Способ получени уксусной кислоты |
Also Published As
| Publication number | Publication date |
|---|---|
| AU6348499A (en) | 2000-05-29 |
| KR100687510B1 (ko) | 2007-02-27 |
| KR20010103633A (ko) | 2001-11-23 |
| ID28477A (id) | 2001-05-31 |
| FR2785606A1 (fr) | 2000-05-12 |
| TW522146B (en) | 2003-03-01 |
| JP4066305B2 (ja) | 2008-03-26 |
| JP2002529436A (ja) | 2002-09-10 |
| CN1216845C (zh) | 2005-08-31 |
| DE69909816D1 (de) | 2003-08-28 |
| EP1127042B1 (fr) | 2003-07-23 |
| US6916952B1 (en) | 2005-07-12 |
| UA68398C2 (en) | 2004-08-16 |
| MY121111A (en) | 2005-12-30 |
| CA2348472A1 (en) | 2000-05-18 |
| DE69909816T2 (de) | 2004-06-03 |
| CA2348472C (en) | 2009-03-31 |
| WO2000027785A1 (fr) | 2000-05-18 |
| EP1127042A1 (fr) | 2001-08-29 |
| ATE245619T1 (de) | 2003-08-15 |
| FR2785606B1 (fr) | 2001-01-26 |
| ES2205888T3 (es) | 2004-05-01 |
| CN1325374A (zh) | 2001-12-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Sen et al. | Mechanism of palladium (II)-catalyzed carbon-carbon double bond isomerization in olefins | |
| CA2223133C (en) | Iridium catalysed carbonylation process for the production of a carboxylic acid | |
| UA26345C2 (uk) | Спосіб одержаhhя оцтової кислоти і каталітичhа система для її одержаhhя | |
| US4906415A (en) | Carrier-supported catalyst and process for making monocarboxylic anhydrides | |
| RU2118310C1 (ru) | Способ получения карбоновых кислот или соответствующих сложных эфиров | |
| KR100636586B1 (ko) | 알콜의카르보닐화방법 | |
| RU96109188A (ru) | Способ карбонилирования алкиловых спиртов и/или их реакционноспособных производных | |
| RU96121014A (ru) | Способ получения уксусной кислоты карбонилированием диметилового эфира | |
| RU2220129C2 (ru) | Способ получения уксусной кислоты и/или метилацетата в присутствии иридия и платины | |
| Oe et al. | Ruthenium catalyzed addition reaction of carboxylic acid across olefins without β-hydride elimination | |
| RU2001111864A (ru) | Способ получения уксусной кислоты и/или метилацетата в присутствии иридия и платины | |
| AU579175B2 (en) | Production of carboxylic acids from alcohols using rhodium complex catalysts | |
| RU2235087C2 (ru) | Способ получения уксусной кислоты и/или метилацетата и способ улучшения стабильности и/или предотвращения дезактивации катализатора при получении уксусной кислоты и/или метилацетата | |
| JP2002529436A5 (enExample) | ||
| CN103506167B (zh) | 一种失活铑膦催化剂的处理方法 | |
| Kelkar et al. | Carbonylation of methanol to acetic acid using homogeneous Ru complex catalyst | |
| RU2068406C1 (ru) | Способ получения адипиновой кислоты | |
| JPH02212453A (ja) | カルボン酸の異性化方法 | |
| EP0614870A2 (en) | Process for producing optically active aldehydes | |
| RU2181355C2 (ru) | Способ получения уксусной кислоты и/или метилацетата посредством изомеризации и карбонилирования | |
| WO2001051445A2 (en) | Co-production of carboxylic acids and/or their esters | |
| JPS5825652B2 (ja) | カルボンサンルイノ セイホウ | |
| Bub et al. | On the rhodium catalyzed formation of acetic acid from methyl formate—comparison with the rhodium catalyzed formation of acetic acid by direct carbonylation of methanol | |
| Yoneda et al. | Acetic acid process catalyzed by ionically immobilized rhodium complex to solid resin support | |
| CN103506166A (zh) | 失活铑膦催化剂的活化方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20131030 |