GB1232015A - - Google Patents
Info
- Publication number
- GB1232015A GB1232015A GB1232015DA GB1232015A GB 1232015 A GB1232015 A GB 1232015A GB 1232015D A GB1232015D A GB 1232015DA GB 1232015 A GB1232015 A GB 1232015A
- Authority
- GB
- United Kingdom
- Prior art keywords
- preference
- olefinic
- bis
- cyclic
- terminal
- 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
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 125000004122 cyclic group Chemical group 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
- 150000001993 dienes Chemical class 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 238000005984 hydrogenation reaction Methods 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 239000000758 substrate Substances 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Substances 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
- AHAREKHAZNPPMI-AATRIKPKSA-N (3e)-hexa-1,3-diene Chemical compound CC\C=C\C=C AHAREKHAZNPPMI-AATRIKPKSA-N 0.000 abstract 1
- QFMZQPDHXULLKC-UHFFFAOYSA-N 1,2-bis(diphenylphosphino)ethane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCP(C=1C=CC=CC=1)C1=CC=CC=C1 QFMZQPDHXULLKC-UHFFFAOYSA-N 0.000 abstract 1
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 abstract 1
- IFVMAGPISVKRAR-UHFFFAOYSA-N 1-ethylcyclohexene Chemical compound CCC1=CCCCC1 IFVMAGPISVKRAR-UHFFFAOYSA-N 0.000 abstract 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 abstract 1
- DMJJSMVXGKXBNI-UHFFFAOYSA-M C(=O)=[Ir]Br Chemical compound C(=O)=[Ir]Br DMJJSMVXGKXBNI-UHFFFAOYSA-M 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- -1 cyclic olefins Chemical class 0.000 abstract 1
- 238000009905 homogeneous catalytic hydrogenation reaction Methods 0.000 abstract 1
- 229910052741 iridium Inorganic materials 0.000 abstract 1
- 229910052762 osmium Inorganic materials 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 abstract 1
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 229910052703 rhodium Inorganic materials 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
- C07C5/08—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of carbon-to-carbon triple bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
- C07C5/03—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of non-aromatic carbon-to-carbon double bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
- C07C5/10—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of aromatic six-membered rings
- C07C5/11—Partial hydrogenation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3462067 | 1967-07-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1232015A true GB1232015A (en:Method) | 1971-05-19 |
Family
ID=10367920
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1232015D Expired GB1232015A (en:Method) | 1967-07-27 | 1967-07-27 |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE718703A (en:Method) |
| DE (1) | DE1793024B1 (en:Method) |
| FR (1) | FR1580556A (en:Method) |
| GB (1) | GB1232015A (en:Method) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2024121371A1 (en) * | 2022-12-09 | 2024-06-13 | Dsm Ip Assets B.V. | Selective hydrogenation |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6111145A (ja) * | 1984-06-28 | 1986-01-18 | Toa Nenryo Kogyo Kk | ジオレフイン類の水素添加用触媒 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE253160C (en:Method) * | 1900-01-01 | |||
| GB1085762A (en) * | 1965-04-30 | 1967-10-04 | Ici Ltd | Complex organic iridium compounds and their use as catalysts |
| GB1135979A (en) * | 1965-06-11 | 1968-12-11 | Ici Ltd | Hydrogenation process |
-
1967
- 1967-07-27 GB GB1232015D patent/GB1232015A/en not_active Expired
-
1968
- 1968-07-25 DE DE19681793024 patent/DE1793024B1/de active Pending
- 1968-07-26 FR FR1580556D patent/FR1580556A/fr not_active Expired
- 1968-07-26 BE BE718703D patent/BE718703A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2024121371A1 (en) * | 2022-12-09 | 2024-06-13 | Dsm Ip Assets B.V. | Selective hydrogenation |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1580556A (en:Method) | 1969-09-05 |
| BE718703A (en:Method) | 1969-01-27 |
| DE1793024B1 (de) | 1972-03-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Goldman et al. | Organometallic C—H bond activation: an introduction | |
| Bennett | Olefin and Acetylene Complexes of Transition Metals. | |
| Green et al. | The activation of carbon-hydrogen bonds | |
| Pandey | Transition metal nitrosyls in organic synthesis and in pollution control | |
| HALPERN | Homogeneous catalysis by coordination compounds | |
| US3642658A (en) | Selective hydrogenation catalysts | |
| GB1081304A (en) | Improvements in or relating to chemical compounds | |
| US3857900A (en) | Hydrogenation of aldehydes using triarylphosphine rhodium halogenoid catalysts | |
| Tsutsui et al. | σ-π rearrangements of organotransition metal compounds | |
| Basset et al. | Steric environment of the active center in methathesis of olefins | |
| Rees et al. | Carbonylation of metal-oxygen bonds; formation of carbalkoxydicarbonylbis (triphenylphosphine) iridium, ROC (O) Ir (CO) 2 (PPh3) 2, by carbonylation of trans-alkoxy (carbonyl) bis (triphenylphosphine) iridium, trans-ROIr (CO)(PPh3) 2 (R= Me, Pr, Ph) | |
| GB1232015A (en:Method) | ||
| Nishiguchi et al. | Transfer hydrogenation and transfer hydrogenolysis: VIII. Hydrogen transfer from amines to olefins catalyzed by heterogeneous and homogeneous catalysts | |
| Noyori | On the nature of carbenoids generated from bicyclo [1.1. 0] butanes and transition metal complexes | |
| Bennett et al. | Nickel Complexes As Hydrosilation Catalysts | |
| Lyon et al. | Use of transition metal complexes as selective hydrogenation catalysts | |
| US5789638A (en) | Hydrogenation of unsaturated polymers using monocyclopentadienyl group IV metal catalysts | |
| Van Bekkum et al. | Activation of the chlorotris (triphenylphosphine) rhodium (I) hydrogenation catalyst by oxygen or hydrogen peroxide | |
| Chelucci et al. | Osmium complexes in catalysis of olefin hydrogenation and isomerization | |
| GB896391A (en) | Organometallic compounds | |
| GB1154937A (en) | Hydrogenation Process | |
| GB1046780A (en) | Improvements in or relating to selective hydrogenation | |
| GB1121643A (en) | Hydrogenation process | |
| US3732329A (en) | Hydrogenation process utilizing homogeneous copper catalysts | |
| US3692864A (en) | Hydrogenation process utilizing homogeneous metal catalysts |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |