GB1326014A - Catalystic carbonylation process - Google Patents
Catalystic carbonylation processInfo
- Publication number
- GB1326014A GB1326014A GB1326014DA GB1326014A GB 1326014 A GB1326014 A GB 1326014A GB 1326014D A GB1326014D A GB 1326014DA GB 1326014 A GB1326014 A GB 1326014A
- Authority
- GB
- United Kingdom
- Prior art keywords
- july
- alcohols
- esters
- produced
- carboxylic acids
- 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
Links
- 230000006315 carbonylation Effects 0.000 title abstract 2
- 238000005810 carbonylation reaction Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 150000001735 carboxylic acids Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 239000003446 ligand Substances 0.000 abstract 2
- 230000000087 stabilizing effect Effects 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 230000021523 carboxylation Effects 0.000 abstract 1
- 238000006473 carboxylation reaction Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 229910052732 germanium Inorganic materials 0.000 abstract 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002527 isonitriles Chemical class 0.000 abstract 1
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- 229910052723 transition metal Inorganic materials 0.000 abstract 1
- 150000003624 transition metals Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—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)
Abstract
1326014 Carboxylic acids and esters JOHNSON MATTHEY & CO Ltd 6 July 1970 [14 July 1969] 15294/73 Divided out of 1326012 Heading C2C Carboxylic acids or esters are produced by the carboxylation of alcohols with CO using as catalyst a composition prepared by adding a stabilizing donor ligand to a solution contain ing a strong acid and any of M 2 <SP>4+</SP>, M 2 (O 2 CR)<SP>n+</SP> 4-n , M 2 (OCSR)<SP>n+</SP> 4-n and M 2 (S 2 CR)<SP>n+</SP> 4-n , wherein n is 1, 2, 3 or 4, R is alkyl or aryl and may be substituted and M is a transition metal. Preferably, a halogen promoter is present. Stabilizing donor ligands are defined as organic isocyanides; other organic compounds, other than alcohols, having in the molecule an atom of an element of Group VB or VIB in a valency state such that it possesses a lone pair of electrons; or a stannous or germanium II halide. In the example acetic acid is produced by the carbonylation of methanol having dissolved therein Rh 2 (O 2 CCH 3 ) 2 , HBF 4 , P(C 6 H 5 ) 3 and CH 3 I.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1529473 | 1969-07-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1326014A true GB1326014A (en) | 1973-08-08 |
Family
ID=10056521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1326014D Expired GB1326014A (en) | 1969-07-14 | 1969-07-14 | Catalystic carbonylation process |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1326014A (en) |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2431481A1 (en) * | 1978-07-19 | 1980-02-15 | Uop Inc | Carbonylation of alkanol to alkanoic acid and ester - using heterogeneous phthalocyanine catalyst with alkyl halide promoter |
| EP0055618A1 (en) * | 1980-12-29 | 1982-07-07 | Monsanto Company | Carbonylation process employing a catalyst stabilised in soluble form |
| EP0081152A1 (en) * | 1981-12-04 | 1983-06-15 | Hoechst Aktiengesellschaft | Process for preparing acetic-anhydride and/or acetic-acid and/or ethylidene diacetate |
| EP0079592A3 (en) * | 1981-11-12 | 1983-07-06 | Union Carbide Corporation | Catalyst stabilization |
| US4433166A (en) * | 1980-12-29 | 1984-02-21 | Monsanto Company | Process for stabilizing carbonylation catalyst in soluble form |
| US4433165A (en) * | 1980-12-29 | 1984-02-21 | Monsanto Company | Process for stabilizing carbonylation catalyst in soluble form |
| EP0114703A1 (en) * | 1983-01-25 | 1984-08-01 | Shell Internationale Researchmaatschappij B.V. | Process for the preparation of carboxylic acids and/or esters |
| WO1985003703A1 (en) * | 1984-02-16 | 1985-08-29 | Bp Chemicals Limited | Carbonylation process improvement |
| US4563309A (en) * | 1984-08-16 | 1986-01-07 | Union Carbide Corporation | Production of carboxylic anhydrides from methyl carboxlyates using rhodium complex catalysts |
| EP0172365A1 (en) * | 1984-08-21 | 1986-02-26 | Hüls Aktiengesellschaft | Process for the preparation of phenylacetic acid and of its derivatives by catalytic rearrangement of benzyl formate and its derivatives |
| US4733006A (en) * | 1980-12-29 | 1988-03-22 | Monsanto Company | Carbonylation process with an alkali metal acetate as catalyst stabilizer |
| US4918222A (en) * | 1984-07-27 | 1990-04-17 | Texaco Inc. | Process for synthesis of N-acetylglycine |
| US4927967A (en) * | 1984-07-20 | 1990-05-22 | Union Carbide Chemicals And Plastics Company Inc. | Production of carboxylic acids from organic formate esters using rhodium complex catalysts |
| US4990654A (en) * | 1984-08-16 | 1991-02-05 | Union Carbide Chemicals And Plastics Company Inc. | Production of acetate esters from alcohols using rhodium complex catalysts |
| US5026907A (en) * | 1984-08-16 | 1991-06-25 | Union Carbide Chemicals And Plastics Technology Corporation | Production of carboxylic acids from alcohols using rhodium complex catalysts and organic ester source |
| US5817869A (en) * | 1995-10-03 | 1998-10-06 | Quantum Chemical Corporation | Use of pentavalent Group VA oxides in acetic acid processing |
| US6031129A (en) * | 1995-10-03 | 2000-02-29 | Quantum Chemical Corporation | Use of pentavalent group VA oxides in acetic acid processing |
| WO2006064178A1 (en) * | 2004-12-17 | 2006-06-22 | Bp Chemicals Limited | Process and catalyst for the manuafacture of acetic acid |
-
1969
- 1969-07-14 GB GB1326014D patent/GB1326014A/en not_active Expired
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2431481A1 (en) * | 1978-07-19 | 1980-02-15 | Uop Inc | Carbonylation of alkanol to alkanoic acid and ester - using heterogeneous phthalocyanine catalyst with alkyl halide promoter |
| EP0055618A1 (en) * | 1980-12-29 | 1982-07-07 | Monsanto Company | Carbonylation process employing a catalyst stabilised in soluble form |
| US4433166A (en) * | 1980-12-29 | 1984-02-21 | Monsanto Company | Process for stabilizing carbonylation catalyst in soluble form |
| US4433165A (en) * | 1980-12-29 | 1984-02-21 | Monsanto Company | Process for stabilizing carbonylation catalyst in soluble form |
| US4733006A (en) * | 1980-12-29 | 1988-03-22 | Monsanto Company | Carbonylation process with an alkali metal acetate as catalyst stabilizer |
| EP0079592A3 (en) * | 1981-11-12 | 1983-07-06 | Union Carbide Corporation | Catalyst stabilization |
| EP0081152A1 (en) * | 1981-12-04 | 1983-06-15 | Hoechst Aktiengesellschaft | Process for preparing acetic-anhydride and/or acetic-acid and/or ethylidene diacetate |
| EP0114703A1 (en) * | 1983-01-25 | 1984-08-01 | Shell Internationale Researchmaatschappij B.V. | Process for the preparation of carboxylic acids and/or esters |
| WO1985003703A1 (en) * | 1984-02-16 | 1985-08-29 | Bp Chemicals Limited | Carbonylation process improvement |
| EP0153834A1 (en) * | 1984-02-16 | 1985-09-04 | BP Chemicals Limited | Carbonylation process improvement |
| US4927967A (en) * | 1984-07-20 | 1990-05-22 | Union Carbide Chemicals And Plastics Company Inc. | Production of carboxylic acids from organic formate esters using rhodium complex catalysts |
| US4918222A (en) * | 1984-07-27 | 1990-04-17 | Texaco Inc. | Process for synthesis of N-acetylglycine |
| US5026907A (en) * | 1984-08-16 | 1991-06-25 | Union Carbide Chemicals And Plastics Technology Corporation | Production of carboxylic acids from alcohols using rhodium complex catalysts and organic ester source |
| US4990654A (en) * | 1984-08-16 | 1991-02-05 | Union Carbide Chemicals And Plastics Company Inc. | Production of acetate esters from alcohols using rhodium complex catalysts |
| US4563309A (en) * | 1984-08-16 | 1986-01-07 | Union Carbide Corporation | Production of carboxylic anhydrides from methyl carboxlyates using rhodium complex catalysts |
| EP0172365A1 (en) * | 1984-08-21 | 1986-02-26 | Hüls Aktiengesellschaft | Process for the preparation of phenylacetic acid and of its derivatives by catalytic rearrangement of benzyl formate and its derivatives |
| US5817869A (en) * | 1995-10-03 | 1998-10-06 | Quantum Chemical Corporation | Use of pentavalent Group VA oxides in acetic acid processing |
| US6031129A (en) * | 1995-10-03 | 2000-02-29 | Quantum Chemical Corporation | Use of pentavalent group VA oxides in acetic acid processing |
| WO2006064178A1 (en) * | 2004-12-17 | 2006-06-22 | Bp Chemicals Limited | Process and catalyst for the manuafacture of acetic acid |
| RU2393918C2 (en) * | 2004-12-17 | 2010-07-10 | Бп Кемикэлз Лимитед | Method and catalyst for producing acetic acid |
| US7977272B2 (en) | 2004-12-17 | 2011-07-12 | Bp Chemicals Limited | Process and catalyst for the manufacture of acetic acid |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PE20 | Patent expired after termination of 20 years |