GB1357207A - Preparation of pyridine or pyridine with 2,6-lutidine as by-product - Google Patents

Preparation of pyridine or pyridine with 2,6-lutidine as by-product

Info

Publication number
GB1357207A
GB1357207A GB5509471A GB5509471A GB1357207A GB 1357207 A GB1357207 A GB 1357207A GB 5509471 A GB5509471 A GB 5509471A GB 5509471 A GB5509471 A GB 5509471A GB 1357207 A GB1357207 A GB 1357207A
Authority
GB
United Kingdom
Prior art keywords
picoline
pyridine
reaction
catalyst
gas
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
GB5509471A
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.)
Stamicarbon BV
Original Assignee
Stamicarbon BV
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 Stamicarbon BV filed Critical Stamicarbon BV
Publication of GB1357207A publication Critical patent/GB1357207A/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

Landscapes

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

Abstract

1357207 Pyridine from α-picoline STAMICARBON NV 26 Nov 1971 [4 Dec 1970] 55094/71 Heading C2C The invention comprises a process for the preparation of pyridine by gas-phase demethylation of α-picoline with steam at 250-360‹ C. in the presence of a metallic hydrogenation catalyst using a contact time of 0À5-15 seconds. Contact times are obtained by dividing the catalyst volume by the volume rate of flow per second of the gas mixture measured at any desired temperature and corrected to the reaction temperature and pressure. It is preferred to employ 4-25 moles of steam per mole of α- picoline in the reaction gas and a preferred catalyst is nickel on alumina or silica gel. Other catalyst metals specified are nickel, cobalt, platinum, palladium and ruthenium. Some 2,6-lutidine is produced during the reaction (#3%)# the amount may be increased by adding hydrogen to the reaction gas, preferably in an amount of 2-20 moles per mole of α-picoline. The gaseous reaction effluent is condensed and may then be extracted, e.g. with benzene and the resulting solution fractionally distilled.
GB5509471A 1970-12-04 1971-11-26 Preparation of pyridine or pyridine with 2,6-lutidine as by-product Expired GB1357207A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL7017718.A NL167158C (en) 1970-12-04 1970-12-04 PROCESS FOR THE PREPARATION OF PYRIDINE BY DEMETHYLATION OF ALFA-PICOLINE.

Publications (1)

Publication Number Publication Date
GB1357207A true GB1357207A (en) 1974-06-19

Family

ID=19811721

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5509471A Expired GB1357207A (en) 1970-12-04 1971-11-26 Preparation of pyridine or pyridine with 2,6-lutidine as by-product

Country Status (14)

Country Link
JP (1) JPS5024316B1 (en)
AT (1) AT310752B (en)
BE (1) BE776165A (en)
BR (1) BR7108022D0 (en)
CA (1) CA949972A (en)
CH (1) CH562796A5 (en)
DE (1) DE2159846A1 (en)
ES (1) ES397650A1 (en)
FR (1) FR2117222A5 (en)
GB (1) GB1357207A (en)
IT (1) IT945266B (en)
NL (1) NL167158C (en)
SE (1) SE391923B (en)
ZA (1) ZA717998B (en)

Also Published As

Publication number Publication date
NL7017718A (en) 1972-06-06
IT945266B (en) 1973-05-10
FR2117222A5 (en) 1972-07-21
SE391923B (en) 1977-03-07
BR7108022D0 (en) 1973-04-12
CH562796A5 (en) 1975-06-13
JPS5024316B1 (en) 1975-08-14
DE2159846A1 (en) 1972-06-22
NL167158C (en) 1981-11-16
ZA717998B (en) 1972-08-30
ES397650A1 (en) 1974-05-16
CA949972A (en) 1974-06-25
NL167158B (en) 1981-06-16
AT310752B (en) 1973-10-10
BE776165A (en) 1972-06-02

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee