GB850405A - Improvements in the production of alkylpyridines and alkylquinolines - Google Patents
Improvements in the production of alkylpyridines and alkylquinolinesInfo
- Publication number
- GB850405A GB850405A GB77958A GB77958A GB850405A GB 850405 A GB850405 A GB 850405A GB 77958 A GB77958 A GB 77958A GB 77958 A GB77958 A GB 77958A GB 850405 A GB850405 A GB 850405A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pyridine
- methyl
- alumina
- ethyl
- alkyl
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
Abstract
Alkylpyridines having a methyl or ethyl group in the 2-, 4- or 6-position and alkyl quinolines having a methyl or ethyl group in the 2-or-4-position in the heterocyclic ring are methylated on the a - carbon atom of the alkyl group by reaction with methanol or methyl chloride in the vapour phase at 350 DEG -500 DEG C. in the presence of an acidic cracking catalyst containing alumina. From any given starting compound a mixture of alkylated products is usually found. For example, in the methylation of methyl pyridine the corresponding ethyl pyridine is formed and this may then be further methylated to the corresponding iso-propyl pyridine and possibly tert-butyl pyridine. The preferred catalyst is alumina but silica-alumina or activated earths such as fullers' earth may be used. The starting materials may have alkyl substituents present in positions other than those specified above. but these groups are unaffected by the reaction. The ethyl and isopropyl pyridines and quinolines produced by the process may be converted to the corresponding vinyl derivatives by dehydrogenation in known manner, for example by passage over a catalyst containing chromium oxide at 425 DEG -650 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB77958A GB850405A (en) | 1958-01-08 | 1958-01-08 | Improvements in the production of alkylpyridines and alkylquinolines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB77958A GB850405A (en) | 1958-01-08 | 1958-01-08 | Improvements in the production of alkylpyridines and alkylquinolines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB850405A true GB850405A (en) | 1960-10-05 |
Family
ID=9710369
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB77958A Expired GB850405A (en) | 1958-01-08 | 1958-01-08 | Improvements in the production of alkylpyridines and alkylquinolines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB850405A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3957792A (en) * | 1973-06-08 | 1976-05-18 | Hoechst Aktiengesellschaft | Process for preparing 2-ethyl-pyridine |
-
1958
- 1958-01-08 GB GB77958A patent/GB850405A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3957792A (en) * | 1973-06-08 | 1976-05-18 | Hoechst Aktiengesellschaft | Process for preparing 2-ethyl-pyridine |
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