SE320355B - - Google Patents
Info
- Publication number
- SE320355B SE320355B SE9326/62A SE932662A SE320355B SE 320355 B SE320355 B SE 320355B SE 9326/62 A SE9326/62 A SE 9326/62A SE 932662 A SE932662 A SE 932662A SE 320355 B SE320355 B SE 320355B
- Authority
- SE
- Sweden
- Prior art keywords
- salt
- transition metal
- carboxylic
- acid
- preferred
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 abstract 9
- 229910052723 transition metal Inorganic materials 0.000 abstract 7
- 150000003624 transition metals Chemical class 0.000 abstract 7
- -1 hydroxy, amino Chemical group 0.000 abstract 5
- 239000002253 acid Substances 0.000 abstract 4
- 150000001735 carboxylic acids Chemical class 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 3
- 229910017052 cobalt Inorganic materials 0.000 abstract 3
- 239000010941 cobalt Substances 0.000 abstract 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 3
- 239000003446 ligand Substances 0.000 abstract 3
- 229930194542 Keto Chemical group 0.000 abstract 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 150000001299 aldehydes Chemical class 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 150000003863 ammonium salts Chemical class 0.000 abstract 2
- 229910052787 antimony Inorganic materials 0.000 abstract 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 2
- 229910052785 arsenic Inorganic materials 0.000 abstract 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 abstract 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 abstract 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 abstract 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000001033 ether group Chemical group 0.000 abstract 2
- 125000000524 functional group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000000468 ketone group Chemical group 0.000 abstract 2
- 229910052698 phosphorus Inorganic materials 0.000 abstract 2
- 239000011574 phosphorus Substances 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 2
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 abstract 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 abstract 1
- 239000004913 cyclooctene Substances 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229940035429 isobutyl alcohol Drugs 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 1
- 150000003003 phosphines Chemical class 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 229930195734 saturated hydrocarbon Natural products 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 230000007704 transition Effects 0.000 abstract 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical group CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C27/00—Processes involving the simultaneous production of more than one class of oxygen-containing compounds
- C07C27/20—Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxo-reaction
- C07C27/22—Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxo-reaction with the use of catalysts which are specific for this process
-
- 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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US134852A US3274263A (en) | 1961-08-30 | 1961-08-30 | Process for olefin hydroformylation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE320355B true SE320355B (en:Method) | 1970-02-09 |
Family
ID=22465305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE9326/62A SE320355B (en:Method) | 1961-08-30 | 1962-08-28 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3274263A (en:Method) |
| ES (1) | ES280340A2 (en:Method) |
| GB (1) | GB988942A (en:Method) |
| SE (1) | SE320355B (en:Method) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3989675A (en) * | 1964-01-24 | 1976-11-02 | The Dow Chemical Company | Oxo process for producing an aldehyde |
| US3448157A (en) * | 1965-09-27 | 1969-06-03 | Shell Oil Co | Hydroformylation of olefins |
| US3448158A (en) * | 1966-01-28 | 1969-06-03 | Shell Oil Co | Hydroformylation of olefins |
| BE758502A (fr) * | 1969-11-06 | 1971-05-05 | Basf Ag | Preparation d'alcools et d'aldehydes |
| DE2145532C3 (de) * | 1971-09-11 | 1975-02-20 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Aufarbeitung von Hydroformylierungsgemischen |
| US4071568A (en) * | 1975-12-12 | 1978-01-31 | Mitsubishi Chemical Industries Limited | Process for producing glycol monoether |
| US4224255A (en) * | 1978-06-15 | 1980-09-23 | General Electric Company | Process for the production of aldehydes and alcohols from olefinically unsaturated compounds by hydroformylation with suppression of olefin hydrogenation |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB614010A (en) * | 1945-06-07 | 1948-12-08 | Du Pont | Synthesis of organic oxygen-containing compounds |
| US2509878A (en) * | 1947-01-02 | 1950-05-30 | Standard Oil Dev Co | Preparation of aldehydes |
| GB638754A (en) * | 1947-05-16 | 1950-06-14 | Du Pont | Improvements in and relating to the synthesis of primary alcohols |
| US2557701A (en) * | 1948-03-19 | 1951-06-19 | Standard Oil Dev Co | Catalytic reaction of olefins with carbon monoxide and hydrogen |
| US2564130A (en) * | 1948-07-24 | 1951-08-14 | Du Pont | One-step butyl alcohol process |
| US2640074A (en) * | 1949-05-18 | 1953-05-26 | Du Pont | Process for synthesis of higher aliphatic oxygen-containing compounds |
| US2757200A (en) * | 1951-03-29 | 1956-07-31 | Exxon Research Engineering Co | Decobalting of oxo aldehydes with nonaqueous oxalic acid |
| GB784629A (en) * | 1955-02-23 | 1957-10-09 | Exxon Research Engineering Co | Improved oxo process |
| US3150188A (en) * | 1960-04-21 | 1964-09-22 | Diamond Alkali Co | Aromatic phosphite catalyst modifiers in the oxo process |
| NL146830C (en:Method) * | 1960-07-22 |
-
1961
- 1961-08-30 US US134852A patent/US3274263A/en not_active Expired - Lifetime
-
1962
- 1962-08-28 ES ES280340A patent/ES280340A2/es not_active Expired
- 1962-08-28 SE SE9326/62A patent/SE320355B/xx unknown
- 1962-08-28 GB GB33067/62A patent/GB988942A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB988942A (en) | 1965-04-14 |
| US3274263A (en) | 1966-09-20 |
| ES280340A2 (es) | 1962-12-16 |
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