GB992136A - Process for the hydroformylation of olefinic compounds - Google Patents
Process for the hydroformylation of olefinic compoundsInfo
- Publication number
- GB992136A GB992136A GB2582762A GB2582762A GB992136A GB 992136 A GB992136 A GB 992136A GB 2582762 A GB2582762 A GB 2582762A GB 2582762 A GB2582762 A GB 2582762A GB 992136 A GB992136 A GB 992136A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pyridine
- hydroformylated
- olefins
- catalyst
- contacting
- 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
-
- 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
- B01J31/20—Carbonyls
-
- 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
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
- B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
-
- 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
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
-
- 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
- B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
Olefins are hydroformylated by contacting with carbon monoxide and hydrogen, preferably at 500 to 5000 p.s.i. 100-300 DEG C., in the presence of a complex of chromium, molybdenum or tungsten and a substituted or unsubstituted pyridine, which includes polynuclear pyridines. Specified pyridines include 2-chloro pyridine, 3 picaline, ethyl nicotinate, quinoline 3-cyano pyridine, entidine and 3,5-dichloropyridine. Examples of products obtainable are 1-heptanal and 1-heptanol, 3-chloro 1-propanal and 3-chlorol propanol, 4-acetoxybutanol and 4-acetoxy butanyl, formyl cyclopentane and hydroxy methyl cyclopentane, diethyl formyl succinate and diethyl (hydroxy methyl) succinate, 4-phenyl butanal and 4-phenyl-1-butanol. In the detailed example wherein the catalyst is prepared in situ from pyridine and the hexacarbonyl of Mo, W, Cr, the effect of the metal on the isomer formed as product is given.ALSO:Macromolecular olefins, e.g. polybutadiene and styrene butadiene copolymer are stated to be hydroformylated by contacting with carbon monoxide and hydrogen and a catalyst which is a complex of Cr, W or Mo and a substituted or unsubstituted pyridine, which includes polynuclear pyridine derivatives especially at elevated pressures and temperatures.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12240761A | 1961-07-07 | 1961-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB992136A true GB992136A (en) | 1965-05-19 |
Family
ID=22402558
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2582762A Expired GB992136A (en) | 1961-07-07 | 1962-07-05 | Process for the hydroformylation of olefinic compounds |
Country Status (4)
Country | Link |
---|---|
DE (1) | DE1214661B (en) |
ES (1) | ES278937A1 (en) |
GB (1) | GB992136A (en) |
SE (1) | SE301142B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5041685A (en) * | 1988-03-22 | 1991-08-20 | Neste Oy | Procedure for producing alcohols and aldehydes from alkenes and synthesis gases |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE874301C (en) * | 1951-05-03 | 1953-04-23 | Basf Ag | Process for the production of alcohols |
DE921931C (en) * | 1952-05-11 | 1955-01-07 | Basf Ag | Process for the production of alcohols and their esters |
DE921932C (en) * | 1952-09-05 | 1955-01-07 | Basf Ag | Process for the production of alcohols |
US2811567A (en) * | 1954-03-09 | 1957-10-29 | Exxon Research Engineering Co | Oxo preparation of high molecular weight alcohols |
-
1962
- 1962-07-05 DE DES80283A patent/DE1214661B/en active Pending
- 1962-07-05 GB GB2582762A patent/GB992136A/en not_active Expired
- 1962-07-05 ES ES0278937A patent/ES278937A1/en not_active Expired
- 1962-07-05 SE SE751862A patent/SE301142B/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5041685A (en) * | 1988-03-22 | 1991-08-20 | Neste Oy | Procedure for producing alcohols and aldehydes from alkenes and synthesis gases |
Also Published As
Publication number | Publication date |
---|---|
SE301142B (en) | 1968-05-27 |
DE1214661B (en) | 1966-04-21 |
ES278937A1 (en) | 1962-12-16 |
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