CH209090A - Process for the preparation of a polyazo dye. - Google Patents

Process for the preparation of a polyazo dye.

Info

Publication number
CH209090A
CH209090A CH209090DA CH209090A CH 209090 A CH209090 A CH 209090A CH 209090D A CH209090D A CH 209090DA CH 209090 A CH209090 A CH 209090A
Authority
CH
Switzerland
Prior art keywords
dye
preparation
parts
polyazo dye
polyazo
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellsc Farbenindustrie
Original Assignee
Ig Farbenindustrie 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 Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Publication of CH209090A publication Critical patent/CH209090A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/16—Trisazo dyes
    • C09B31/26—Trisazo dyes from other coupling components "D"
    • C09B31/28—Heterocyclic compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02—Disazo dyes
    • C09B35/039—Disazo dyes characterised by the tetrazo component
    • C09B35/28—Disazo dyes characterised by the tetrazo component the tetrazo component containing two aryl nuclei linked by at least one of the groups —CON<, —SO2N<, —SO2—, or —SO2—O—
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/36—Trisazo dyes of the type
    • C09B35/374—D contains two aryl nuclei linked by at least one of the groups —CON<, —SO2N<, —SO2—, or —SO2—O—
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

  

      Zusatzpatent    zum     Hauptpatent    Nr. 203426.    Verfahren zur Herstellung eines     Polyazofarbstoffes.       Gegenstand des vorliegenden Patentes ist  ein Verfahren zur Herstellung     eines        Polyazo-          farbstoffes.    Das Verfahren ist dadurch ge-    kennzeichnet, dass man den nach dem 'Ver  fahren der     schweiz.    Patentschrift Nr.

   190894  erhältlichen     Disazofarbstoff    der Konstitution  
EMI0001.0009     
         diazotiert,    mit dein Kondensationsprodukt aus  m - Ami     nophenyl    - 5 -     pyrazolon    - 3     -carbonsäure     und dein Chlorid des     4-Carboxy-2-nitrophenyl-          ätliylsulfons    kuppelt und die Nitrogruppe zur       Aminogruppe    reduziert. Der neue Farbstoff  stellt ein hellbraunes Pulver dar, das Baum  wolle nach dem     Diazotieren    und Entwickeln  mit     ss-Naphthol    in gelben Tönen färbt.  



  <I>Beispiel:</I>  219 Teile     1-(3'-Aminophenyl)-5-pyrazolon-          3-carbonsäure    in 800 Teilen     Pyridin    gelöst    werden     portionsweise    mit<B>555</B> Teilen des  Chlorids aus     4-Carboxy-2-nitrophenyl-äthyl-          sulfon    versetzt. Nach längerem Stehen wird  das abgekühlte, feste Reaktionsprodukt mit  Wasser verrührt, das abgeschiedene Konden  sationsprodukt isoliert. Es löst sich mit Soda  in Wasser klar auf und lässt sich nicht mehr       diazotieren.     



  46 Teile des so erhältlichen Kondensa  tionsproduktes werden in Wasser gelöst, mit  30 Teilen Soda vermischt und mit der     Di-          azoverbindung    aus 65 Teilen des Körpers    
EMI0002.0001     
    die nach dein D. R. P. 632135 zugängig ist,  vereinigt. Der Farbstoff wird nach vollendeter  Kupplung auf<B>800</B> erwärmt und mit 42 Tei  len Schwefelnatrium kristallisiert in Wasser  reduziert, nach beendigter Reduktion     ausge-          salzen,    gepresst und getrocknet. Er färbt auf  Baumwolle nach dein     Diazotieren    und Ent  wickeln mit     P-Naphthol    ein Gelb.



      Additional patent to main patent no. 203426. Process for the production of a polyazo dye. The present patent relates to a process for the production of a polyazo dye. The procedure is characterized by the fact that the procedure of Switzerland is used. Patent No.

   190894 available disazo dye of the constitution
EMI0001.0009
         diazotized, with your condensation product of m - Ami nophenyl - 5 - pyrazolone - 3 -carboxylic acid and your chloride of 4-carboxy-2-nitrophenyl ätliylsulfons coupled and reduced the nitro group to the amino group. The new dye is a light brown powder which, after diazotizing and developing with ss-naphthol, dyes the cotton in yellow tones.



  <I> Example: </I> 219 parts of 1- (3'-aminophenyl) -5-pyrazolone-3-carboxylic acid are dissolved in 800 parts of pyridine in portions with <B> 555 </B> parts of the chloride from 4-carboxy -2-nitrophenyl-ethyl sulfone added. After standing for a long time, the cooled, solid reaction product is stirred with water, and the precipitated condensation product is isolated. It dissolves clear in water with soda and can no longer be diazotized.



  46 parts of the condensation product obtainable in this way are dissolved in water, mixed with 30 parts of soda and with the di-azo compound from 65 parts of the body
EMI0002.0001
    which is accessible according to your D. R. P. 632135, united. After coupling is complete, the dye is heated to 800 and reduced with 42 parts of sodium sulphide, crystallized in water, then salted out, pressed and dried after the reduction is complete. After diazotizing and developing with p-naphthol, it dyes cotton a yellow.

Claims (1)

PATEN TANSPRUCII Verfahren zur Herstellung eines Polyazo- farbstoffes, dadurch gekennzeichnet, dass man den nach dem Verfahren der Schweiz. Patent schrift Nr. 190894 erhältlichen Disazofarbstoff der Konstitution EMI0002.0010 diazotiert, mit dem Kondensationsprodukt aus m-Aminophenyl-5-pyrazolon-3-carbonsäure und dem Chlorid des 4-Carboxy-2-nitropheny 1 äthyIsulfons kuppelt und die Nitrogruppe zur Aminogruppe reduziert. PATEN TANSPRUCII Process for the production of a polyazo dye, characterized in that the process of Switzerland. U.S. Patent No. 190894 disazo dye of the constitution EMI0002.0010 diazotized, coupled with the condensation product of m-aminophenyl-5-pyrazolone-3-carboxylic acid and the chloride of 4-carboxy-2-nitropheny 1 äthyIsulfons and reduced the nitro group to the amino group. Der neue Farbstoff stellt ein hellbraunes Pulver dar, das Baumwolle nach dem Diazo- tieren und Entwickeln mit P-Naphthol in gelben Tönen färbt. The new dye is a light brown powder that dyes cotton in yellow tones after diazotizing and developing with P-naphthol.
CH209090D 1937-02-26 1938-01-18 Process for the preparation of a polyazo dye. CH209090A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE203426X 1937-02-26

Publications (1)

Publication Number Publication Date
CH209090A true CH209090A (en) 1940-03-15

Family

ID=25723930

Family Applications (3)

Application Number Title Priority Date Filing Date
CH209090D CH209090A (en) 1937-02-26 1938-01-18 Process for the preparation of a polyazo dye.
CH210730D CH210730A (en) 1937-02-26 1938-01-18 Process for the preparation of a polyazo dye.
CH203426D CH203426A (en) 1937-02-26 1938-01-18 Process for the preparation of a polyazo dye.

Family Applications After (2)

Application Number Title Priority Date Filing Date
CH210730D CH210730A (en) 1937-02-26 1938-01-18 Process for the preparation of a polyazo dye.
CH203426D CH203426A (en) 1937-02-26 1938-01-18 Process for the preparation of a polyazo dye.

Country Status (2)

Country Link
CH (3) CH209090A (en)
FR (1) FR833819A (en)

Also Published As

Publication number Publication date
CH210730A (en) 1940-07-31
CH203426A (en) 1939-03-15
FR833819A (en) 1938-11-02

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