FR1365413A - Procédé de préparation d'aluminium-alcoyles et d'alcools primaires - Google Patents
Procédé de préparation d'aluminium-alcoyles et d'alcools primairesInfo
- Publication number
- FR1365413A FR1365413A FR934772A FR934772A FR1365413A FR 1365413 A FR1365413 A FR 1365413A FR 934772 A FR934772 A FR 934772A FR 934772 A FR934772 A FR 934772A FR 1365413 A FR1365413 A FR 1365413A
- Authority
- FR
- France
- Prior art keywords
- aluminium
- ene
- catalyst
- compound
- olefin
- 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
- 238000000034 method Methods 0.000 title abstract 4
- 238000002360 preparation method Methods 0.000 title abstract 2
- 150000003138 primary alcohols Chemical class 0.000 title abstract 2
- 239000003054 catalyst Substances 0.000 abstract 8
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 abstract 6
- 125000005234 alkyl aluminium group Chemical group 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 239000004411 aluminium Substances 0.000 abstract 3
- 229910052782 aluminium Inorganic materials 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 methylates Chemical compound 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 229910052804 chromium Inorganic materials 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical compound CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 abstract 2
- 229910052719 titanium Inorganic materials 0.000 abstract 2
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052720 vanadium Inorganic materials 0.000 abstract 2
- QHOMPCGOCNNMFK-ACCUITESSA-N (e)-tridec-6-ene Chemical compound CCCCCC\C=C\CCCCC QHOMPCGOCNNMFK-ACCUITESSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052776 Thorium Inorganic materials 0.000 abstract 1
- 229910003074 TiCl4 Inorganic materials 0.000 abstract 1
- 229910052770 Uranium Inorganic materials 0.000 abstract 1
- 125000005595 acetylacetonate group Chemical group 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium chloride Substances Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 1
- 150000001399 aluminium compounds Chemical class 0.000 abstract 1
- 229910000091 aluminium hydride Inorganic materials 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- 230000005587 bubbling Effects 0.000 abstract 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 238000004523 catalytic cracking Methods 0.000 abstract 1
- 239000013522 chelant Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- UURSXESKOOOTOV-UHFFFAOYSA-N dec-5-ene Chemical compound CCCCC=CCCCC UURSXESKOOOTOV-UHFFFAOYSA-N 0.000 abstract 1
- 230000018044 dehydration Effects 0.000 abstract 1
- 238000006297 dehydration reaction Methods 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 150000004707 phenolate Chemical class 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 abstract 1
- 229940031826 phenolate Drugs 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 238000000746 purification Methods 0.000 abstract 1
- 150000003873 salicylate salts Chemical class 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 229910052715 tantalum Inorganic materials 0.000 abstract 1
- 238000004227 thermal cracking Methods 0.000 abstract 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 abstract 1
- ZQDPJFUHLCOCRG-AATRIKPKSA-N trans-3-hexene Chemical compound CC\C=C\CC ZQDPJFUHLCOCRG-AATRIKPKSA-N 0.000 abstract 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 abstract 1
- 229910052721 tungsten Inorganic materials 0.000 abstract 1
- 229910052726 zirconium Inorganic materials 0.000 abstract 1
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
- C07C29/48—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups
- C07C29/50—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only
- C07C29/54—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only starting from compounds containing carbon-to-metal bonds and followed by conversion of the -O- metal to -OH groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/061—Aluminium compounds with C-aluminium linkage
- C07F5/062—Al linked exclusively to C
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB39814/63A GB1019968A (en) | 1962-05-16 | 1962-12-19 | Process for the preparation of alkyl aluminium compounds and primary alcohols |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FR1365413A true FR1365413A (fr) | 1964-07-03 |
Family
ID=10411645
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR934772A Expired FR1365413A (fr) | 1962-12-19 | 1963-05-14 | Procédé de préparation d'aluminium-alcoyles et d'alcools primaires |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3322806A (fr) |
| BE (1) | BE632318A (fr) |
| DE (2) | DE1211203B (fr) |
| FR (1) | FR1365413A (fr) |
| GB (2) | GB1004108A (fr) |
| NL (1) | NL292758A (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3475477A (en) * | 1962-11-13 | 1969-10-28 | Shell Oil Co | Process for the production of aluminum alkyls |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3382269A (en) * | 1964-12-30 | 1968-05-07 | Continental Oil Co | Activation of aluminum in preparation of aluminum alkyls |
| US5124465A (en) * | 1991-03-25 | 1992-06-23 | Ethyl Corporation | Aluminum alkyls and linear 1-olefins from internal olefins |
| US5144053A (en) * | 1991-03-25 | 1992-09-01 | Ethyl Corporation | Aluminum alkyls and linear 1-olefins from internal olefins |
| US5191145A (en) * | 1991-03-25 | 1993-03-02 | Ethyl Corporation | Continuous process for preparing aluminum alkyls and linear 1-olefins from internal olefins |
| US5274153A (en) * | 1991-03-25 | 1993-12-28 | Ethyl Corporation | Continuous process for preparing aluminum alkyls and linear 1-olefins from internal olefins |
| US5276220A (en) * | 1992-06-18 | 1994-01-04 | Ethyl Corporation | Actinide catalyzed chain growth process |
| US5430165A (en) * | 1992-06-29 | 1995-07-04 | Albemarle Corporation | Method of oxidizing aluminum alkyls |
| US5233103A (en) * | 1992-06-29 | 1993-08-03 | Ethyl Corporation | Preparation of organoaluminum compounds and linear alcohols derived therefrom |
| US5597937A (en) * | 1995-05-11 | 1997-01-28 | Albemarle Corporation | Conversion of deep internal olefins into primary alkylaluminum compounds by isomerization-displacement |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2959607A (en) * | 1959-06-29 | 1960-11-08 | Grace W R & Co | Higher aluminum alkyls and products therefrom |
-
1962
- 1962-05-16 GB GB18856/62A patent/GB1004108A/en not_active Expired
- 1962-12-19 GB GB39814/63A patent/GB1019968A/en not_active Expired
-
1963
- 1963-05-13 US US280098A patent/US3322806A/en not_active Expired - Lifetime
- 1963-05-14 BE BE632318A patent/BE632318A/nl unknown
- 1963-05-14 DE DES94200A patent/DE1211203B/de active Pending
- 1963-05-14 DE DES85219A patent/DE1207388B/de active Pending
- 1963-05-14 FR FR934772A patent/FR1365413A/fr not_active Expired
- 1963-05-15 NL NL292758D patent/NL292758A/nl unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3475477A (en) * | 1962-11-13 | 1969-10-28 | Shell Oil Co | Process for the production of aluminum alkyls |
Also Published As
| Publication number | Publication date |
|---|---|
| NL292758A (fr) | 1965-07-26 |
| DE1211203B (de) | 1966-02-24 |
| GB1019968A (en) | 1966-02-09 |
| DE1207388B (de) | 1965-12-23 |
| BE632318A (nl) | 1963-11-18 |
| US3322806A (en) | 1967-05-30 |
| GB1004108A (en) | 1965-09-08 |
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