GB1005984A - Manufacture of pyridine and alkylpyridines - Google Patents

Manufacture of pyridine and alkylpyridines

Info

Publication number
GB1005984A
GB1005984A GB2872063A GB2872063A GB1005984A GB 1005984 A GB1005984 A GB 1005984A GB 2872063 A GB2872063 A GB 2872063A GB 2872063 A GB2872063 A GB 2872063A GB 1005984 A GB1005984 A GB 1005984A
Authority
GB
United Kingdom
Prior art keywords
acetaldehyde
acrolein
boron
phosphorus
oxygen
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
GB2872063A
Inventor
Alastair Campbell
Ian Campbell
John Anthony Corran
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2872063A priority Critical patent/GB1005984A/en
Priority to DE1963R0035670 priority patent/DE1295158B/en
Publication of GB1005984A publication Critical patent/GB1005984A/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
    • C07D213/09Preparation by ring-closure involving the use of ammonia, amines, amine salts, or nitriles
    • C07D213/10Preparation by ring-closure involving the use of ammonia, amines, amine salts, or nitriles from acetaldehyde or cyclic polymers thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Pyridine, methyl pyridines and methyl-ethyl pyridines are prepared by contacting a gaseous mixture containing acetaldehyde and ammonia at an elevated temperature with a catalyst containing a compound or compounds of boron, phosphorus and oxygen. The reaction mixture may also contain acrolein, preferably in an amount of 0.3 to 3.0 moles per mole of acetaldehyde, and/or diluent gases or vapours. It is preferably not to contact ammonia with acetaldehyde at a temperature below 200 DEG C., suitable reaction temperatures being between 250 DEG and 500 DEG C. The acetaldehyde and acrolein reactants may be added as such, in the form of a reaction product containing a reactant, e.g. the product of the catalytic oxidation of propene for acrolein, or a material giving rise to it under the reaction conditions, e.g. paraldehyde for acetaldehyde. The compound(s) of boron, phosphorus and oxygen is (are) preferably deposited on a support material, advantageously by impregnating the carrier with an aqueous solution containing boric and phosphoric acids and subsequently drying and calcining the impregnated material.
GB2872063A 1962-07-26 1963-05-16 Manufacture of pyridine and alkylpyridines Expired GB1005984A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB2872063A GB1005984A (en) 1963-05-16 1963-05-16 Manufacture of pyridine and alkylpyridines
DE1963R0035670 DE1295158B (en) 1962-07-26 1963-07-13 Solid fuel space heater

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2872063A GB1005984A (en) 1963-05-16 1963-05-16 Manufacture of pyridine and alkylpyridines

Publications (1)

Publication Number Publication Date
GB1005984A true GB1005984A (en) 1965-09-29

Family

ID=10280019

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2872063A Expired GB1005984A (en) 1962-07-26 1963-05-16 Manufacture of pyridine and alkylpyridines

Country Status (1)

Country Link
GB (1) GB1005984A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2378764A1 (en) * 1977-01-26 1978-08-25 Degussa PROCESS FOR THE PREPARATION OF PYRIDINE AND 3-METHYLPYRIDINE
EP2277864A1 (en) * 2009-06-24 2011-01-26 Lonza Ltd. Synthesis process for 3-methylpyridine

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2378764A1 (en) * 1977-01-26 1978-08-25 Degussa PROCESS FOR THE PREPARATION OF PYRIDINE AND 3-METHYLPYRIDINE
US4147874A (en) * 1977-01-26 1979-04-03 Deutsche Gold- Und Silber Scheideanstalt Vormals Roessler Process for the production of pyridine and 3-methyl pyridine
EP2277864A1 (en) * 2009-06-24 2011-01-26 Lonza Ltd. Synthesis process for 3-methylpyridine
WO2010149352A3 (en) * 2009-06-24 2011-06-23 Lonza Ltd Synthesis process for 3-methylpyridine
CN102803215A (en) * 2009-06-24 2012-11-28 隆萨有限公司 Synthesis process for 3-methylpyridine
CN102803215B (en) * 2009-06-24 2014-04-30 隆萨有限公司 Synthesis process for 3-methylpyridine
US9701634B2 (en) 2009-06-24 2017-07-11 Lonza Ltd Process for the synthesis of 3-methyl-pyridine

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