GB878746A - Transalkylation of organo-metallo compounds - Google Patents
Transalkylation of organo-metallo compoundsInfo
- Publication number
- GB878746A GB878746A GB30178/58A GB3017858A GB878746A GB 878746 A GB878746 A GB 878746A GB 30178/58 A GB30178/58 A GB 30178/58A GB 3017858 A GB3017858 A GB 3017858A GB 878746 A GB878746 A GB 878746A
- Authority
- GB
- United Kingdom
- Prior art keywords
- olefin
- preferred
- compound
- reaction period
- transalkylation
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/32—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen
- C07C1/325—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a metal atom
- C07C1/327—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a metal atom the hetero-atom being an aluminium atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
A process for the transalkylation of organometallic compounds while inhibiting the formation of dimers comprises reacting said compound with an olefin while maintaining less than 6%, preferably less than 3% by weight of said olefin in said organometallic compound throughout the reaction period. The organometallic compound may be of the formula RxMHy where R is substituted or unsubstituted alkyl, aryl, alkaryl, aralkyl, cycloalkyl, alkenyl, aralkenyl or cycloalkenyl radical having 2 to 35 carbon atoms, M is a metal, preferably aluminium, antimony, bismuth, cadmium, copper, gallium, germanium, indium, lead, tin, mercury, thallium or zinc, (x+y) is the valency of M and y is 0 or 1. Preferred olefines have 2 to 40 carbon atoms in the molecule. At least 1/100% by weight of olefin should be present throughout the reaction period. In order to facilitate the reaction and maintain the concentration of olefine within the desired limits it is preferred to maintain the organo-aluminium compound in the liquid phase and the olefin in the gaseous phase. Thus it is preferred to carry out the process at a temperature between 0 DEG and 300 DEG C., a pressure from 1 mm Hg to 1000 lbs/sq inch absolute and a reaction period from 0.1 to 30 hours.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US878746XA | 1957-12-05 | 1957-12-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB878746A true GB878746A (en) | 1961-10-04 |
Family
ID=22207769
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB30178/58A Expired GB878746A (en) | 1957-12-05 | 1958-09-22 | Transalkylation of organo-metallo compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB878746A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002066406A1 (en) * | 2001-01-25 | 2002-08-29 | Basf Aktiengesellschaft | Modified method for producing higher $g(a)-olefin |
-
1958
- 1958-09-22 GB GB30178/58A patent/GB878746A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002066406A1 (en) * | 2001-01-25 | 2002-08-29 | Basf Aktiengesellschaft | Modified method for producing higher $g(a)-olefin |
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