EP0762933A1 - Oxydative ammonolyse von alkylpyridinen - Google Patents

Oxydative ammonolyse von alkylpyridinen

Info

Publication number
EP0762933A1
EP0762933A1 EP94926183A EP94926183A EP0762933A1 EP 0762933 A1 EP0762933 A1 EP 0762933A1 EP 94926183 A EP94926183 A EP 94926183A EP 94926183 A EP94926183 A EP 94926183A EP 0762933 A1 EP0762933 A1 EP 0762933A1
Authority
EP
European Patent Office
Prior art keywords
catalytic composition
process according
methyl
catalyst
ethylpyridine
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.)
Ceased
Application number
EP94926183A
Other languages
English (en)
French (fr)
Inventor
Boris Viktorovitch Suvorov
Lidija Anatoljevna Stepanova
Nadezhda Antonovna Belova
Roderick John Chuck
Daniel Pianzola
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.)
Lonza AG
INSTITUTE OF CHEMICAL SCIENCE OF NATIONAL ACADEMY OF SCIENCE OF REPUBLIC KAZAKSTAN
Original Assignee
Lonza AG
INSTITUTE OF CHEMICAL SCIENCE OF NATIONAL ACADEMY OF SCIENCE OF REPUBLIC KAZAKSTAN
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 Lonza AG, INSTITUTE OF CHEMICAL SCIENCE OF NATIONAL ACADEMY OF SCIENCE OF REPUBLIC KAZAKSTAN filed Critical Lonza AG
Publication of EP0762933A1 publication Critical patent/EP0762933A1/de
Ceased 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
    • C07D213/60Heterocyclic 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 with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/84Nitriles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/20Vanadium, niobium or tantalum
    • B01J23/22Vanadium

Definitions

  • This invention relates to a process for the preparation of a highly selective catalyst for the production of cyanopyridines by oxidative ammonolysis of alkylpyridines and to a process for the preparation of cyanopyridines.
  • the invention is especially directed to the production of 3-cyanopyridine or cyanopyridine derivatives which are important precursors for nicotinic acid or nicotinic acid amide. Nicotinic acid or nicotinic acid amide are essential vitamins of the B-complex.
  • a 1 b is 7.5 to 8 c is 0 to 0.5 x represents the number of oxygen atoms necessary to satisfy the valency requirements of the elements present follows according to claim 1 the steps of coprecipitating a solution of a $ + - and of a Ti" ⁇ + - and optionally of a Zr ⁇ + -compound in water with a solution of ammonia in water, by a subsequent exposure of the precipitate to a drying treatment and to a heat treatment and by a shaping step in order to bring the catalytic composition in a suitable catalyst form.
  • V Tig O x catalyst was prepared according to example a), catalyst preparation- but with the difference that the heat treatment of the tablets was conducted at a temperature of 850 °C for 2 hours.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pyridine Compounds (AREA)
EP94926183A 1994-05-23 1994-08-11 Oxydative ammonolyse von alkylpyridinen Ceased EP0762933A1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KZ940560 1994-05-23
KZ9405601 1994-05-23
PCT/EP1994/002677 WO1995032054A1 (en) 1994-05-23 1994-08-11 Oxidative ammonolysis of alkylpyridines

Publications (1)

Publication Number Publication Date
EP0762933A1 true EP0762933A1 (de) 1997-03-19

Family

ID=19720744

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94926183A Ceased EP0762933A1 (de) 1994-05-23 1994-08-11 Oxydative ammonolyse von alkylpyridinen

Country Status (13)

Country Link
EP (1) EP0762933A1 (de)
JP (1) JP4161119B2 (de)
KR (1) KR100331727B1 (de)
AU (1) AU7612694A (de)
BG (1) BG100989A (de)
BR (1) BR9408577A (de)
CA (1) CA2188655A1 (de)
FI (1) FI964649A7 (de)
HU (1) HUT76437A (de)
NO (1) NO964990D0 (de)
PL (1) PL317319A1 (de)
SK (1) SK149696A3 (de)
WO (1) WO1995032054A1 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2428505A2 (de) 2010-09-13 2012-03-14 Jubilant Life Sciences Limited Verfahren zur Herstellung von Pyridincarboxylsäuren

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2305377A1 (de) 2009-09-29 2011-04-06 Lonza Ltd. Katalysatoren zum Herstellen von Cyanopyridinen und ihre Verwendung
EP2319834A1 (de) * 2009-10-16 2011-05-11 Lonza Ltd. Verfahren und Vorrichtungen zur Herstellung von wässrigen Lösungen von Cyanopyridinen

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2505745C3 (de) * 1974-03-14 1980-01-03 Showa Denko K.K., Tokio Verfahren zur kontinuierlichen Herstellung von 3-Cyanopyridin
DE2510994B2 (de) * 1975-03-13 1977-04-14 Basf Ag, 6700 Ludwigshafen Vanadium- und titanhaltiger traegerkatalysator
DE2547655A1 (de) * 1975-10-24 1977-04-28 Basf Ag Verfahren zur herstellung von halogensubstituierten anthrachinonen
DE3866774D1 (de) * 1987-05-12 1992-01-23 Nippon Catalytic Chem Ind Verfahren zur herstellung aromatischer oder heterocyclischer nitrile.
US5021386A (en) * 1990-03-21 1991-06-04 Texaco Inc. Compositions involving V2 O3 -ZRO2 -TIO2

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9532054A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2428505A2 (de) 2010-09-13 2012-03-14 Jubilant Life Sciences Limited Verfahren zur Herstellung von Pyridincarboxylsäuren

Also Published As

Publication number Publication date
BR9408577A (pt) 1997-08-19
FI964649L (fi) 1997-01-21
FI964649A7 (fi) 1997-01-21
BG100989A (en) 1997-08-29
CA2188655A1 (en) 1995-11-30
NO964990L (no) 1996-11-22
NO964990D0 (no) 1996-11-22
JPH10500892A (ja) 1998-01-27
PL317319A1 (en) 1997-04-01
AU7612694A (en) 1995-12-18
SK149696A3 (en) 1997-05-07
KR100331727B1 (ko) 2002-06-20
FI964649A0 (fi) 1996-11-21
WO1995032054A1 (en) 1995-11-30
HUT76437A (en) 1997-08-28
HU9603235D0 (en) 1997-01-28
JP4161119B2 (ja) 2008-10-08

Similar Documents

Publication Publication Date Title
CN107537537B (zh) 一种用于氨氧化反应制备2-氰基吡啶的催化剂
JPS6299360A (ja) 3−メチルピリジン及び3−メチルピペリジンの混合物からの3−シアノピリジンの製造方法
CZ338596A3 (en) Catalytic mixture for oxidative amonolysis of alkyl pyridines, process of its preparation and use
WO1995032054A1 (en) Oxidative ammonolysis of alkylpyridines
US7795169B2 (en) Process for preparing cyanopyridines and suitable catalysts therefor
US5028713A (en) Ammoxidation of methyl substituted heteroaromatics to make heteroaromatic nitriles
US3970659A (en) Preparation of cyanopyridines
CN1151135C (zh) 一种用于制备3-氰基吡啶的催化剂及其制备方法和用途
CN100390147C (zh) 杂芳腈的制备方法,其改良的催化剂及所述改良催化剂的制备方法
US2839535A (en) Process for the manufacture of nitriles
RU2126716C1 (ru) Каталитическая система для окислительного аммонолиза алкилпиридинов, способ ее получения и способ окислительного аммонолиза алкилпиридинов
CN107011255B (zh) 一种由甲基吡啶制备氨基吡啶的方法及其纯化方法
US3981879A (en) Preparation of cyanopyridines
US5910465A (en) Process for the preparation of a highly active and selective ammoxidation catalyst and its use in preparing heteroaromatic nitriles
OKADA et al. Studies on the Ammoxidation of N-Heterocyclic Compounds. IV. Vapor-Phase Ammoxidation of Lutidine Isomers
JP4321880B2 (ja) 2−メチル−1,5−ペンタンジアミンからの3−シアノピリジンの製造方法
JP3941121B2 (ja) アルキルピリジンの酸化アンモノリシスのための触媒組成物
KR101767696B1 (ko) 메틸피리딘의 제조를 위한 촉매
US4118388A (en) Process for producing pyridine
CN109096184B (zh) 一种吡啶甲酸类化合物的制备方法
JP4373515B2 (ja) アシルピリジンの製造方法
JP2002226461A (ja) アシルピリジン類の製造方法
JP2019202940A (ja) 六員複素環骨格を有する化合物の製造方法
MXPA96005500A (en) Catalytic composition for the oxidative ozonolisis of alquilpiridi
JPS5817189B2 (ja) 3− シアノピリジン ノ セイゾウホウ

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19961120

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LI NL PT SE

AX Request for extension of the european patent

Free format text: LT PAYMENT 961120;SI PAYMENT 961120

17Q First examination report despatched

Effective date: 19970429

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 19971204