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ES8207121A1 - Procedimiento de fabricacion de la 2,6-dicloro-4-nitroanili-na - Google Patents

Procedimiento de fabricacion de la 2,6-dicloro-4-nitroanili-na

Info

Publication number
ES8207121A1
ES8207121A1 ES502698A ES502698A ES8207121A1 ES 8207121 A1 ES8207121 A1 ES 8207121A1 ES 502698 A ES502698 A ES 502698A ES 502698 A ES502698 A ES 502698A ES 8207121 A1 ES8207121 A1 ES 8207121A1
Authority
ES
Spain
Prior art keywords
nitroaniline
dichloro
preparation
compound obtained
paranitroaniline
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
ES502698A
Other languages
English (en)
Other versions
ES502698A0 (es
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 CropScience SA
Original Assignee
Rhone Poulenc Agrochimie SA
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 Rhone Poulenc Agrochimie SA filed Critical Rhone Poulenc Agrochimie SA
Publication of ES502698A0 publication Critical patent/ES502698A0/es
Publication of ES8207121A1 publication Critical patent/ES8207121A1/es
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/68Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
    • C07C209/74Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton by halogenation, hydrohalogenation, dehalogenation, or dehydrohalogenation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00Compounds containing amino groups bound to a carbon skeleton
    • C07C211/43Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C211/44Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring
    • C07C211/45Monoamines
    • C07C211/46Aniline

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

PROCEDIMIENTO DE OBTENCION DE 2,6-DICLORO-4-NITROANILINA. CONSISTE EN LA CLORACION MEDIANTE CLORO GASEOSO DE LA PARANITROANILINA EN SOLUCION ACUOSA DE ACIDO CLORHIDRICO, CON EBULLICION. LA REACCION TIENE LUGAR A UNA TEMPERATURA COMPRENDIDA ENTRE 95 Y 110 GRADOS CENTIGRADOS. LA CONCENTRACION DEL MEDIO ACIDO OSCILA ENTRE 4 Y 7,5 N. PREFERENTEMENTE SE TRABAJA CON UNA CONCENTRACION DE 1 MOL DE AMINA POR LITRO DE ACIDO CLORHIDRICO. ES NECESARIO QUE AL FINAL DE LA OPERACION NO RE SULTE SOBRESTURADO EL MEDIO, YA QUE DE SER ASI SE DESGASARIA EL ACIDO EN EXCESO Y COMPETIRIA CON EL CLORO EN SU PASO HACIA EL LIQUIDO, LO QUE AUMENTARIA LA DURACION DE LA REACCION.
ES502698A 1980-06-06 1981-06-02 Procedimiento de fabricacion de la 2,6-dicloro-4-nitroanili-na Expired ES8207121A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8013021A FR2483914A1 (fr) 1980-06-06 1980-06-06 Procede de fabrication de la dichloro-2,6-nitro-4-aniline et compose obtenu par ce procede

Publications (2)

Publication Number Publication Date
ES502698A0 ES502698A0 (es) 1982-04-01
ES8207121A1 true ES8207121A1 (es) 1982-04-01

Family

ID=9242985

Family Applications (1)

Application Number Title Priority Date Filing Date
ES502698A Expired ES8207121A1 (es) 1980-06-06 1981-06-02 Procedimiento de fabricacion de la 2,6-dicloro-4-nitroanili-na

Country Status (20)

Country Link
US (1) US4414415A (es)
EP (1) EP0041908B1 (es)
JP (1) JPS5731646A (es)
KR (1) KR840000518B1 (es)
AT (1) ATE6421T1 (es)
BR (1) BR8103561A (es)
CA (1) CA1211128A (es)
DD (1) DD159425A5 (es)
DE (1) DE3162422D1 (es)
DK (1) DK158975C (es)
ES (1) ES8207121A1 (es)
FR (1) FR2483914A1 (es)
GB (1) GB2077261B (es)
HU (1) HU185930B (es)
IE (1) IE51755B1 (es)
IL (1) IL62869A (es)
RO (1) RO81213B (es)
SU (1) SU1079174A3 (es)
YU (1) YU42243B (es)
ZA (1) ZA813744B (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3418495A1 (de) * 1984-05-18 1985-11-21 Hoechst Ag, 6230 Frankfurt Verfahren zur herstellung von 2,6-dichlor-4-nitroanilin
EP0192612B1 (de) * 1985-02-22 1988-05-25 Ciba-Geigy Ag Verfahren zur Herstellung von Chlornitroanilinen und Chlornitrophenolen
US5068443A (en) * 1990-06-01 1991-11-26 Noram Chemical Company Process for the manufacture of 2,6-dichloro-4-nitroaniline
CN103073434B (zh) * 2013-01-09 2014-07-23 寿光市鲁源盐化有限公司 2,6-二溴-4-硝基苯胺和溴素的联产方法及联产装置

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA507950A (en) * 1954-12-07 Celanese Corporation Of America Dyestuff intermediates
DE432801C (de) * 1924-07-15 1926-08-14 Chem Fab Von Heyden Ag Fa Verfahren zur Herstellung von 2-Chlor-4-nitro-1-aminobenzol
US3396195A (en) * 1965-10-11 1968-08-06 Upjohn Co Process for making 2, 6-dichloro-4-nitroaniline
US3396200A (en) * 1967-06-02 1968-08-06 Atomic Energy Commission Usa Preparation of 2, 4, 6-trichloronitrobenzene
GB1241771A (en) * 1969-03-31 1971-08-04 Reckitt & Colmann Prod Ltd Improvements in or relating to the chlorination of amines
US3890388A (en) * 1974-03-04 1975-06-17 Du Pont Ring chlorination of ortho-toluidine
DE2648054C3 (de) * 1976-10-23 1982-01-21 Basf Ag, 6700 Ludwigshafen Verfahren zur Herstellung von Dichlornitroanilinen

Also Published As

Publication number Publication date
RO81213B (ro) 1983-02-28
DK246481A (da) 1981-12-07
ES502698A0 (es) 1982-04-01
JPS6212787B2 (es) 1987-03-20
YU42243B (en) 1988-06-30
YU141781A (en) 1983-06-30
KR830006172A (ko) 1983-09-17
IL62869A (en) 1984-09-30
BR8103561A (pt) 1982-03-02
CA1211128A (en) 1986-09-09
GB2077261A (en) 1981-12-16
GB2077261B (en) 1984-07-11
ATE6421T1 (de) 1984-03-15
JPS5731646A (en) 1982-02-20
SU1079174A3 (ru) 1984-03-07
IL62869A0 (en) 1981-07-31
DK158975C (da) 1991-01-07
FR2483914B1 (es) 1983-11-04
FR2483914A1 (fr) 1981-12-11
RO81213A (ro) 1983-02-15
ZA813744B (en) 1982-06-30
DK158975B (da) 1990-08-13
EP0041908B1 (fr) 1984-02-29
DD159425A5 (de) 1983-03-09
US4414415A (en) 1983-11-08
HU185930B (en) 1985-04-28
EP0041908A1 (fr) 1981-12-16
IE51755B1 (en) 1987-03-18
KR840000518B1 (ko) 1984-04-17
DE3162422D1 (en) 1984-04-05
IE811240L (en) 1981-12-06

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19980204