JPS5442391A - Recovery of catalyst for hydroformylation of olefins - Google Patents
Recovery of catalyst for hydroformylation of olefinsInfo
- Publication number
- JPS5442391A JPS5442391A JP10858977A JP10858977A JPS5442391A JP S5442391 A JPS5442391 A JP S5442391A JP 10858977 A JP10858977 A JP 10858977A JP 10858977 A JP10858977 A JP 10858977A JP S5442391 A JPS5442391 A JP S5442391A
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- alcohol
- tertiary amine
- unsaturated compound
- subject
- 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.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To separate for reuse catalyst without causing insolubles to crystallize after distillation of the subject products from reaction products obtained in the synthesis of alcohols from olefins over the Rh-tertiary amine catalyst.
CONSTITUTION: An olefinic unsaturated compound (for example, 1-hexene), in the presence of the Rh-tertiary amine catalyst (for example, Rh(CO)4Cl2. N-methyl- pyrrolindine), is reacted with an oxo gas, consisting of H2 and CO, charged by the addition of a solvent (for example, polyethylene glycol) of a higher boiling poing than that of the alcohol formed under the conditions of 20 to 300kg/cm2 and 50 to 200°C. Subsequently, from the reaction products, the subject alcohol (for example, heptyl alcohol) and N-methylphyrrolidine are separated by means of evaporation, and then the residual liquor containing catalyst is further made to perform oxo- reaction by the addition of an olefinic unsaturated compound and a tertiary amine in the same manner as the previous process. Thus, the alcohol can be recovered in high yield as in the previous process.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10858977A JPS5442391A (en) | 1977-09-09 | 1977-09-09 | Recovery of catalyst for hydroformylation of olefins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10858977A JPS5442391A (en) | 1977-09-09 | 1977-09-09 | Recovery of catalyst for hydroformylation of olefins |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9633580A Division JPS5929171B2 (en) | 1980-07-15 | 1980-07-15 | Method for hydroformylating olefins |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5442391A true JPS5442391A (en) | 1979-04-04 |
JPS5551623B2 JPS5551623B2 (en) | 1980-12-25 |
Family
ID=14488628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10858977A Granted JPS5442391A (en) | 1977-09-09 | 1977-09-09 | Recovery of catalyst for hydroformylation of olefins |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5442391A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6225508B1 (en) * | 1997-07-07 | 2001-05-01 | Hoechst Research & Technology Deutschland Gmbh & Co. Kg | Method for producing alkanals using a rhodium-tri-polyethylene glycolate |
JP2006117590A (en) * | 2004-10-22 | 2006-05-11 | Tosoh F-Tech Inc | Method for recycling catalyst and solvent |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5857249U (en) * | 1981-10-14 | 1983-04-18 | 東芝テック株式会社 | Charging control circuit in charging equipment |
-
1977
- 1977-09-09 JP JP10858977A patent/JPS5442391A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6225508B1 (en) * | 1997-07-07 | 2001-05-01 | Hoechst Research & Technology Deutschland Gmbh & Co. Kg | Method for producing alkanals using a rhodium-tri-polyethylene glycolate |
JP2006117590A (en) * | 2004-10-22 | 2006-05-11 | Tosoh F-Tech Inc | Method for recycling catalyst and solvent |
Also Published As
Publication number | Publication date |
---|---|
JPS5551623B2 (en) | 1980-12-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4062884A (en) | Process for the preparation of dialkylcarbonates | |
US3670032A (en) | Preparation of unsaturated alcohols and ethers | |
KR950003254A (en) | Process for preparing acetic acid ester | |
US4473655A (en) | Method for the recovery of rhodium complexes | |
US3028417A (en) | Process of making hydroxy ester compounds | |
US4308397A (en) | Preparation of alkyl alkoxyacetates | |
JPS5442391A (en) | Recovery of catalyst for hydroformylation of olefins | |
US3965132A (en) | Acid and ester production | |
US2021869A (en) | Production of vinyl ethers | |
US4350668A (en) | Recovery of cobalt component from 3-pentenoic ester synthesis | |
DE2635566C3 (en) | Process for the preparation of oxirane compounds by cracking a corresponding alkylene glycol monoester | |
US3974194A (en) | Method of separating cobalt catalyst from a liquid polyol ester product | |
US2472086A (en) | Carburetor process for acetylene reactions | |
US3878058A (en) | Recovery of alkylvinylether by extractive distillation of a feed containing only trace amounts of water | |
JPS579736A (en) | Preparation of fatty acid or its derivative | |
JPS6140658B2 (en) | ||
US4275252A (en) | Oxo alcohol synthesis with rhodium catalyst recycle | |
JPS57156442A (en) | Preparation of methyl lactate | |
US4374287A (en) | Synthesis of alcohols | |
JPS5268115A (en) | Preparation of unsaturated ketones | |
US2217167A (en) | Process for the production of ethers of butanol-1-one-3 | |
JPS5615229A (en) | Production of alkoxypropanol | |
JPS5655323A (en) | Hydroformylation of olefins | |
Takegami et al. | Studies of the Organic Reactions of Metal Carbonyls. XIII. The Reduction of Olefin Oxides with Potassium Iron Carbonylates | |
US3165556A (en) | Preparation of divinyl and tetravinyl ethers of pentaerythritol |