GB788671A - Improvements in and relating to the production of alkyl aluminium compounds - Google Patents
Improvements in and relating to the production of alkyl aluminium compoundsInfo
- Publication number
- GB788671A GB788671A GB1164955A GB1164955A GB788671A GB 788671 A GB788671 A GB 788671A GB 1164955 A GB1164955 A GB 1164955A GB 1164955 A GB1164955 A GB 1164955A GB 788671 A GB788671 A GB 788671A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aluminium
- alkyl
- pressure
- give
- reacted
- 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
- 125000005234 alkyl aluminium group Chemical group 0.000 title abstract 4
- 239000004411 aluminium Substances 0.000 abstract 9
- 229910052782 aluminium Inorganic materials 0.000 abstract 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 8
- -1 alkyl aluminium halide Chemical class 0.000 abstract 3
- 229910000091 aluminium hydride Inorganic materials 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000012442 inert solvent Substances 0.000 abstract 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 239000012190 activator Substances 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 150000001350 alkyl halides Chemical class 0.000 abstract 1
- 239000012298 atmosphere Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 238000000354 decomposition reaction Methods 0.000 abstract 1
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 abstract 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 abstract 1
- 238000003801 milling Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000012299 nitrogen atmosphere Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 238000002360 preparation method Methods 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
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- C07F5/065—Aluminium compounds with C-aluminium linkage compounds with an Al-H linkage
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Metallic aluminium is reacted with an aluminium alkyl and hydrogen at elevated temperature and pressure to give an alkyl aluminium hydride. The reaction may be carried out at a temperature within the range 60 DEG to 200 DEG C. (preferably about 100 DEG to about 140 DEG C.), and under a pressure of at least 150 atmospheres. The reaction temperature should not exceed the decomposition temperature of the alkyl aluminium hydride. The aluminium should preferably be free from oxide coating; this may be removed by milling the rod submerged in an inert solvent in the absence of oxygen. Preferably the reaction is conducted in the presence of an alkyl halide (ethyl iodide or n-propyl bromide) or an alkyl aluminium halide as activator, and of an inert solvent such as a paraffinic or alicyclic hydrocarbon. Water and oxygen should not be present, the preparation being carried out in an inert atmosphere of, e.g., nitrogen. The alkyl aluminium hydrides may be used as catalysts in the polymerization of olefins, or may be reacted with a -olefines at elevated temperature and pressure to produce aluminium trialkyls, thus dipropyl aluminium hydride reacts with propylene to give aluminium tripropyl. In an example finely-divided aluminium is suspended in a solution of aluminium triethyl in methylcyclohexane and heated in an autoclave in the presence of hydrogen at 100 DEG C. and 250 atmospheres pressure. The aluminium sesquibromide with sodium. The product was filtered in a nitrogen atmosphere to give a solution containing ethyl aluminium hydrides. This solution was then reacted with ethylene at 100 DEG C. and 100 atmospheres pressure to give a solution containing aluminium triethyl.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1164955A GB788671A (en) | 1955-04-22 | 1955-04-22 | Improvements in and relating to the production of alkyl aluminium compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1164955A GB788671A (en) | 1955-04-22 | 1955-04-22 | Improvements in and relating to the production of alkyl aluminium compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB788671A true GB788671A (en) | 1958-01-08 |
Family
ID=9990138
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1164955A Expired GB788671A (en) | 1955-04-22 | 1955-04-22 | Improvements in and relating to the production of alkyl aluminium compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB788671A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1100023B (en) * | 1957-12-03 | 1961-02-23 | Pechiney Prod Chimiques Sa | Process and device for the activation of metallic aluminum used for the production of organic aluminum compounds |
US3026345A (en) * | 1958-02-05 | 1962-03-20 | Koppers Co Inc | Process for producing dialkyl aluminum hydrides |
-
1955
- 1955-04-22 GB GB1164955A patent/GB788671A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1100023B (en) * | 1957-12-03 | 1961-02-23 | Pechiney Prod Chimiques Sa | Process and device for the activation of metallic aluminum used for the production of organic aluminum compounds |
US3026345A (en) * | 1958-02-05 | 1962-03-20 | Koppers Co Inc | Process for producing dialkyl aluminum hydrides |
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