GB793215A - Hydrocarbon conversion process - Google Patents
Hydrocarbon conversion processInfo
- Publication number
- GB793215A GB793215A GB4969/56A GB496956A GB793215A GB 793215 A GB793215 A GB 793215A GB 4969/56 A GB4969/56 A GB 4969/56A GB 496956 A GB496956 A GB 496956A GB 793215 A GB793215 A GB 793215A
- Authority
- GB
- United Kingdom
- Prior art keywords
- iodine
- carbon atom
- quaternary carbon
- reaction
- hydrocarbon
- 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
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/42—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
- C07C5/44—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor with halogen or a halogen-containing compound as an acceptor
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aliphatic hydrocarbons containing at least six carbon atoms, at least one of which is a quaternary carbon atom, are heated with iodine or a compound which yields iodine under reaction conditions at an elevated temperature to give a different hydrocarbon by effecting bond cleavage and converting at least one quaternary carbon atom to a non-quaternary carbon atom. Reactions which may occur are isomerization, cyclization, dehydrogenation, aromatization, and dealkylation. The aliphatic hydrocarbon may be an alkane or alkene and preferably contains one quaternary carbon atom in a chain of at least five carbon atoms. The reaction may be carried out in the liquid or vapour phase in the presence of inert solids or catalysts or with a diluent. Temperatures of 300-600 DEG C. are preferred at atmospheric pressure with reaction times of 0.01 second to 5 minutes. The amount of iodine varies according to the desired reaction and particularly on the extent of dehydrogenation, and is preferably in the range 0.05 to 4 equivalents of iodine for each equivalent of hydrogen to be removed. Alkyl iodides such as ethyl, propyl or hexyl iodides may replace iodine as the reactant. In a typical example, 2,2,4-trimethyl pentane and iodine in an iodine/hydrocarbon ratio of 0.31 were heated in the vapour phase at 444 DEG C. and atmospheric pressure for 26 seconds. Xylenes, isobutane and isobutene were recovered as the principal products.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US793215XA | 1955-02-18 | 1955-02-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB793215A true GB793215A (en) | 1958-04-09 |
Family
ID=22149803
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4969/56A Expired GB793215A (en) | 1955-02-18 | 1956-02-17 | Hydrocarbon conversion process |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB793215A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1174752B (en) * | 1959-11-24 | 1964-07-30 | Shell Int Research | Process for the production of p-terphenyl in addition to cumene |
-
1956
- 1956-02-17 GB GB4969/56A patent/GB793215A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1174752B (en) * | 1959-11-24 | 1964-07-30 | Shell Int Research | Process for the production of p-terphenyl in addition to cumene |
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