[go: up one dir, main page]

GB923348A - Production of alkyl-substituted pyridines - Google Patents

Production of alkyl-substituted pyridines

Info

Publication number
GB923348A
GB923348A GB586561A GB586561A GB923348A GB 923348 A GB923348 A GB 923348A GB 586561 A GB586561 A GB 586561A GB 586561 A GB586561 A GB 586561A GB 923348 A GB923348 A GB 923348A
Authority
GB
United Kingdom
Prior art keywords
ammonia
substituted pyridines
propoxypropionaldehyde
propoxybutyraldehyde
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
Application number
GB586561A
Inventor
Kenneth Raymond Hargrave
Leslie Ernest Cooper
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB586561A priority Critical patent/GB923348A/en
Publication of GB923348A publication Critical patent/GB923348A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/06Heterocyclic 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
    • C07D213/08Preparation by ring-closure

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)

Abstract

Alkyl-substituted pyridines are produced by heating together ammonia and an alkoxyaldehyde of formula R1OCHR2CHR3-CHO, in which R1 is a primary alkyl group and R2 and R3 are primary alkyl groups or hydrogen. The process is preferably carried out at a temperature of 300-500 DEG C. in the presence of a condensation catalyst. Suitable alkoxyaldehydes are, for example, 3-propoxypropionaldehyde, 3-propoxybutyraldehyde or methoxyvaleraldehyde. Suitable catalysts are, for example, those containing silica and/or alumina. The catalysts may also contain titania, zirconia, ceria or thoria and zinc, cadmium, tin, lead, tungsten, nickel, cobalt, chromium, molybdenum, iron, copper, palladium or silver or a compound thereof. In the examples (a) 3-propoxypropionaldehyde is reacted with ammonia to give b -picoline and (b) 3-propoxybutyraldehyde is reacted with ammonia to give 3,4-lutidine.
GB586561A 1961-02-17 1961-02-17 Production of alkyl-substituted pyridines Expired GB923348A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB586561A GB923348A (en) 1961-02-17 1961-02-17 Production of alkyl-substituted pyridines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB586561A GB923348A (en) 1961-02-17 1961-02-17 Production of alkyl-substituted pyridines

Publications (1)

Publication Number Publication Date
GB923348A true GB923348A (en) 1963-04-10

Family

ID=9804067

Family Applications (1)

Application Number Title Priority Date Filing Date
GB586561A Expired GB923348A (en) 1961-02-17 1961-02-17 Production of alkyl-substituted pyridines

Country Status (1)

Country Link
GB (1) GB923348A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116371417A (en) * 2023-03-06 2023-07-04 济南悟通生物科技有限公司 Catalyst for synthesizing 3, 4-dimethyl pyrrole and preparation method and application thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116371417A (en) * 2023-03-06 2023-07-04 济南悟通生物科技有限公司 Catalyst for synthesizing 3, 4-dimethyl pyrrole and preparation method and application thereof
CN116371417B (en) * 2023-03-06 2023-10-03 济南悟通生物科技有限公司 Catalyst for synthesizing 3, 4-dimethyl pyrrole and preparation method and application thereof

Similar Documents

Publication Publication Date Title
GB923348A (en) Production of alkyl-substituted pyridines
GB790824A (en) Improvements in the compound di-(2,2,2-trifluoroethyl) acetal of acetaldehyde, process for producing the compound, and process for producing 2,2,2-trifluoroethyl vinyl ether
BR6353212D0 (en) PROCESS FOR THE PRODUCTION OF ETHYLENE OXIDE BY PARTIAL OXIDATION OF ETHYLENE THROUGH GASEOUS OXYGEN IN THE PRESENCE OF A CATALYST CONTAINING SILVER
GB1022638A (en) Process for transforming acetonitrile
GB732269A (en) Preparation of fluorinated organic compounds
ES451620A1 (en) Condensation products
GB898869A (en) Synthesis of 3-4:lutidine
GB920526A (en) Production of pyridine bases
GB964993A (en) Production of 3-ethyl-4-methylpyridine and 2-n-propyl pyridine
GB1241854A (en) Production of diaminodicyclohexylalkanes or ethers
GB887688A (en) Production of beta-picoline
GB924527A (en) Production of pyridine bases
GB1123320A (en) A process for the production of adamantane
GB923347A (en) Production of alkyl pyridines
GB906528A (en) Production of alkyl pyridines
JPS5615221A (en) Manufacture of alkylbenzene
GB917765A (en) Production of pyridine bases
GB971174A (en) Production of pyridine
GB896051A (en) Production of ª--picoline
GB900799A (en) Production of alpha-picoline and gamma-picoline
GB1446135A (en) Process for preparation of a palladium complex compound
GB963887A (en) Production of pyridine and ª‰-picoline
GB896049A (en) Production of ª--picoline
GB907059A (en) Production of pyridine bases
GB1208291A (en) Catalytic process for the manufacture of pyridine and methylpyridines