GB971174A - Production of pyridine - Google Patents

Production of pyridine

Info

Publication number
GB971174A
GB971174A GB3129961A GB3129961A GB971174A GB 971174 A GB971174 A GB 971174A GB 3129961 A GB3129961 A GB 3129961A GB 3129961 A GB3129961 A GB 3129961A GB 971174 A GB971174 A GB 971174A
Authority
GB
United Kingdom
Prior art keywords
pyridine
crotonaldehyde
formaldehyde
ammonia
silica
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
GB3129961A
Inventor
Leslie Ernest Cooper
Kenneth Raymond Hargrave
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 GB3129961A priority Critical patent/GB971174A/en
Priority to SE884262A priority patent/SE323676B/xx
Publication of GB971174A publication Critical patent/GB971174A/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

Abstract

Pyridine is prepared by reacting in the vapour phase at elevated temperature, a mixture of formaldehyde, crotonaldehyde and ammonia, the formaldehyde being in a molar excess over the crotonaldehyde. The ammonia may be added to the treated aldehydes preferably in a temperature range 300 DEG C. to 500 DEG C. and in the presence of a condensation catalyst such as silica, alumina or a mixture thereof which may be admixed with titania, zirconia, ceria or thoria, and contain one or more metal or compound thereof such as zinc, cadmium, tin, lead, tungsten, nickel, cobalt, chromium, molybdenum, iron, palladium or silver. Picolines may be present in the product which is fractionally distilled to yield pyridine. Examples describe processes using silica/alumina admixed with lead fluoride as a catalyst.
GB3129961A 1961-08-31 1961-08-31 Production of pyridine Expired GB971174A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB3129961A GB971174A (en) 1961-08-31 1961-08-31 Production of pyridine
SE884262A SE323676B (en) 1961-08-31 1962-08-14

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3129961A GB971174A (en) 1961-08-31 1961-08-31 Production of pyridine

Publications (1)

Publication Number Publication Date
GB971174A true GB971174A (en) 1964-09-30

Family

ID=10321074

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3129961A Expired GB971174A (en) 1961-08-31 1961-08-31 Production of pyridine

Country Status (2)

Country Link
GB (1) GB971174A (en)
SE (1) SE323676B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0040698A1 (en) * 1980-05-23 1981-12-02 Lonza Ag Process for the preparation of 3-picoline

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0040698A1 (en) * 1980-05-23 1981-12-02 Lonza Ag Process for the preparation of 3-picoline
US4337342A (en) * 1980-05-23 1982-06-29 Lonza Ltd. Process for the preparation of 3-picoline

Also Published As

Publication number Publication date
SE323676B (en) 1970-05-11

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