ES2064512T3 - Procedimiento para la obtencion de 2-cloro-5-clorometil-piridina y nuevos productos intermedios. - Google Patents

Procedimiento para la obtencion de 2-cloro-5-clorometil-piridina y nuevos productos intermedios.

Info

Publication number
ES2064512T3
ES2064512T3 ES90106721T ES90106721T ES2064512T3 ES 2064512 T3 ES2064512 T3 ES 2064512T3 ES 90106721 T ES90106721 T ES 90106721T ES 90106721 T ES90106721 T ES 90106721T ES 2064512 T3 ES2064512 T3 ES 2064512T3
Authority
ES
Spain
Prior art keywords
procedure
chlorometil
piridina
alcalatas
chloro
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 - Lifetime
Application number
ES90106721T
Other languages
English (en)
Inventor
Klaus Dr Jelich
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Application granted granted Critical
Publication of ES2064512T3 publication Critical patent/ES2064512T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/61—Halogen atoms or nitro radicals

Landscapes

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

Abstract

SE PONE A PUNTO UN NUEVO PROCEDIMIENTO PARA LA PRODUCCION DE 2-CLORO-5-CLOROMETIL-PIRIDINA. EL PROCEDIMIENTO SE CARACTERIZA PORQUE SE HACEN REACCIONAR DERIVADOS DE 2-ALCOXI-5-ALCOXIMETIL-PIRIDINA CON UN AGENTE DE CLORACION, EVENTUALMENTE EN PRESENCIA DE UN DISOLVENTE Y DE UN ADYUVANTE DE REACCION, A TEMPERATURAS COMPRENDIDAS ENTRE 0 (GRADOS) C Y 200 (GRADOS) C. LAS VENTAJAS DEL PROCEDIMIENTO ESTAN EN EL FACIL ACCESO A LOS NUEVOS DERIVADOS DE 2-ALCOXI-5-ALCOXIMETILPIRIDINA POR REACCION DE 3-DICLOROMETILPIRIDINA CON UN ALCOHOL Y CON LOS CORRESPONDIENTES ALCOHOLATOS DE METAL ALCALINO, A TEMPERATURAS ENTRE 0 (GRADOS) Y 200 (GRADOS) C, ASI COMO EN EL ESCASO NUMERO DE PASOS DE LA SINTESIS Y EN LA UTILIZACION PARA LA SINTESIS DE PRODUCTOS QUIMICOS BARATOS, PUDIENDO UTILIZARSE COMO COMPUESTO BASICO 3-METILPIRIDINA. EL COMPUESTO 2-CLORO-5-CLOROMETIL-PIRIDINA PUEDE UTILIZARSE COMO PRODUCTO INTERMEDIO PARA LA PRODUCCION DE INSECTICIDAS.
ES90106721T 1989-04-20 1990-04-07 Procedimiento para la obtencion de 2-cloro-5-clorometil-piridina y nuevos productos intermedios. Expired - Lifetime ES2064512T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE3912964A DE3912964A1 (de) 1989-04-20 1989-04-20 Verfahren zur herstellung von 2-chlor-5-chlormethyl-pyridin und neue zwischenprodukte

Publications (1)

Publication Number Publication Date
ES2064512T3 true ES2064512T3 (es) 1995-02-01

Family

ID=6379050

Family Applications (1)

Application Number Title Priority Date Filing Date
ES90106721T Expired - Lifetime ES2064512T3 (es) 1989-04-20 1990-04-07 Procedimiento para la obtencion de 2-cloro-5-clorometil-piridina y nuevos productos intermedios.

Country Status (6)

Country Link
US (1) US5116993A (es)
EP (1) EP0393453B1 (es)
JP (1) JP2865797B2 (es)
KR (1) KR0143987B1 (es)
DE (2) DE3912964A1 (es)
ES (1) ES2064512T3 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR930023342A (ko) * 1992-05-12 1993-12-18 비트 라우버, 토마스 케플러 2-클로로-5-클로로메틸- 피리딘의 제조방법
DE4446338A1 (de) * 1994-12-23 1996-06-27 Bayer Ag Verfahren zur Herstellung von Chlormethylpyridinen
DE102006015467A1 (de) 2006-03-31 2007-10-04 Bayer Cropscience Ag Substituierte Enaminocarbonylverbindungen
RU2316547C1 (ru) * 2006-05-04 2008-02-10 Институт нефтехимии и катализа РАН Способ получения 3-дихлорметилпиридина
DE102006033572A1 (de) 2006-07-20 2008-01-24 Bayer Cropscience Ag N'-Cyano-N-halogenalkyl-imidamid Derivate
EP2039678A1 (de) * 2007-09-18 2009-03-25 Bayer CropScience AG Verfahren zum Herstellen von 4-Aminobut-2-enoliden
EP2107058A1 (de) 2008-03-31 2009-10-07 Bayer CropScience AG Substituierte Enaminothiocarbonylverbindungen
EP2264008A1 (de) 2009-06-18 2010-12-22 Bayer CropScience AG Substituierte Enaminocarbonylverbindungen
WO2012062740A1 (de) 2010-11-12 2012-05-18 Bayer Cropscience Ag Verfahren zur herstellung von 2,2-difluorethylamin-derivaten ausgehend von n-(2,2-difluorethyl)prop-2-en-1-amin
WO2012152741A1 (de) 2011-05-10 2012-11-15 Bayer Intellectual Property Gmbh Bicyclische (thio)carbonylamidine

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2695902A (en) * 1950-09-27 1954-11-30 Merck & Co Inc 2-methyl-3-(beta-chloroethyl)-4, 6-dichloro pyridine and method of making same
JPS5543017A (en) * 1978-09-22 1980-03-26 Ishihara Sangyo Kaisha Ltd Preparation of 2-chloro-5-trichloromethylpyridine
AU548249B2 (en) * 1981-05-13 1985-12-05 Imperial Chemical Industries Plc Production of 3-trichloromethyl and 3-trifluoro methyl- pyridines
US4576629A (en) * 1984-03-15 1986-03-18 Union Carbide Corporation Herbicidal thiadiazole ureas
ZW5085A1 (en) * 1984-04-13 1985-09-18 Nihon Tokushu Noyaku Seizo Kk Nitromethylene derivatives,intermediates thereof,processes for production thereof,and insecticides
DE3630046A1 (de) * 1986-09-04 1988-03-17 Bayer Ag Verfahren zur herstellung von 5-chlormethylpyridinen

Also Published As

Publication number Publication date
JPH11140053A (ja) 1999-05-25
KR0143987B1 (ko) 1998-07-15
JPH02292262A (ja) 1990-12-03
DE59007794D1 (de) 1995-01-12
KR900016133A (ko) 1990-11-12
US5116993A (en) 1992-05-26
EP0393453A2 (de) 1990-10-24
JP2865797B2 (ja) 1999-03-08
DE3912964A1 (de) 1990-10-25
EP0393453A3 (de) 1991-04-17
EP0393453B1 (de) 1994-11-30

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