GB1041101A - Oxo process - Google Patents
Oxo processInfo
- Publication number
- GB1041101A GB1041101A GB2664A GB2664A GB1041101A GB 1041101 A GB1041101 A GB 1041101A GB 2664 A GB2664 A GB 2664A GB 2664 A GB2664 A GB 2664A GB 1041101 A GB1041101 A GB 1041101A
- Authority
- GB
- United Kingdom
- Prior art keywords
- temperature
- oxonation
- propylene
- reactor
- hydrogen
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
In a process for the preparation of alcohols by the oxo process wherein olefins are reacted with carbon monoxide and hydrogen in the presence of a cobalt catalyst at superatmospheric pressures, the improvement comprises controlling the temperature of the reaction mixture to provide a continuously increasing temperature, the initial temperature being 50-178 DEG C., the mid-point temperature 180-200 DEG C. and the terminal temperature 205-225 DEG C. The oxonation is effected in the presence of known cobalt sources, e.g. cobalt carbonyl, carboxylate, oxide, carbonate or metal, yielding in the reaction mixture cobalt carbonyl which is effective as both the carbonylation and hydrogenation catalyst. The preferred amount of hydrogen in the feed and product gas is less than 60% volume and 3-50% volume, respectively, based on total CO + H2 volume. In a preferred embodiment using a tubular reactor, the percentage of hydrogen in the gas phase decreases along the reactor and the numerical product of the value of this H2 percentage multiplied by the temperature at a particular point lies in the range 1500-10,000. It is preferred to introduce 2-10% by weight, based on total reaction mass, of water into the reactor. The process can be carried out, continuously or batchwise, in a tubular reactor, a series of autoclaves or a combination of tubular reactors and stirred autoclaves. Examples describe the oxonation of (1) propylene trimer to isodecyl alcohol, (7) propylene to n- and i-butyl alcohols, (8) heptene to isodecyl alcohol, (9), (10), (11) and (12), propylene tetramer to tridecyl alcohol. In Examples (2)-(6) temperatures outside the scope of the invention are used in the oxonation of propylene trimer to give reaction products containing considerable proportions of isodecylaldehyde.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2664A GB1041101A (en) | 1964-01-01 | 1964-01-01 | Oxo process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2664A GB1041101A (en) | 1964-01-01 | 1964-01-01 | Oxo process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1041101A true GB1041101A (en) | 1966-09-01 |
Family
ID=9697055
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2664A Expired GB1041101A (en) | 1964-01-01 | 1964-01-01 | Oxo process |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1041101A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010527969A (en) * | 2007-05-23 | 2010-08-19 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | Hydroformylation process |
| JP2010527968A (en) * | 2007-05-23 | 2010-08-19 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | Hydroformylation process |
| US7781620B2 (en) | 2006-12-21 | 2010-08-24 | Shell Oil Company | Hydroformylation process |
-
1964
- 1964-01-01 GB GB2664A patent/GB1041101A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7781620B2 (en) | 2006-12-21 | 2010-08-24 | Shell Oil Company | Hydroformylation process |
| JP2010527969A (en) * | 2007-05-23 | 2010-08-19 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | Hydroformylation process |
| JP2010527968A (en) * | 2007-05-23 | 2010-08-19 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | Hydroformylation process |
| US8017810B2 (en) | 2007-05-23 | 2011-09-13 | Shell Oil Company | Hydroformulation process |
| US8017811B2 (en) | 2007-05-23 | 2011-09-13 | Shell Oil Company | Hydroformylation process |
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