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CH285002A - Process for the preparation of a copper-compatible tetrakisazo dye. - Google Patents

Process for the preparation of a copper-compatible tetrakisazo dye.

Info

Publication number
CH285002A
CH285002A CH285002DA CH285002A CH 285002 A CH285002 A CH 285002A CH 285002D A CH285002D A CH 285002DA CH 285002 A CH285002 A CH 285002A
Authority
CH
Switzerland
Prior art keywords
parts
dye
copper
preparation
compatible
Prior art date
Application number
Other languages
German (de)
Inventor
Ag J R Geigy
Original Assignee
Ag J R Geigy
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 Ag J R Geigy filed Critical Ag J R Geigy
Publication of CH285002A publication Critical patent/CH285002A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/38Trisazo dyes ot the type
    • C09B35/40Trisazo dyes ot the type the component K being a dihydroxy or polyhydroxy compound

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

Description

  

  <B>Zusatzpatent</B> zum Hauptpatent Nr. 282092.    Verfahren zur Herstellung eines kupferbaren     Tetrakisazofarbstoffes.    \         Gegenstand.    vorliegenden Patentes ist ein  Verfahren zur Herstellung eines kupferbaren       Tetrakisazofarbstoffes.    Das Verfahren ist da  durch     -ekennzeiehnet,    dass man 1     Mol    der  
EMI0001.0006     
    und anderseits mit 1     Mol        3-Methyl-5-pyrazolon     vereinigt.  



       1-.)ei-    erhaltene nette     Tetrakisazofarbstoff     stellt ein     dunkles    Pulver dar und löst sich in  Wasser und     konz.    Schwefelsäure mit brauner  Farbe.  



  <I>Beispiel:</I>  Man dianotiert 17,2 Teile     1-Arrrinobenzol-3-          sulfonsäure    mit 6,9 Teilen     Natriumnitrit    in  bekannter Weise und kuppelt in     Anwesen-          heit        von        14,6        Teilen        30%iger        Natronlauge     und 25 Teilen     Natriumcarbonat    mit 16,0 Teilen       1-Acetylarnino-2-oxy-benzol.    Ist die Kupplung  fertig, wird der Farbstoff durch Erhitzen mit  verdünnter Natronlauge verseift, mit,

   verdünn  ter     Sehwefelsäure    kalt ausgefällt und     abfil-          triert.    Man löst nun den Farbstoff in Wasser       und        17        Teilen        30%iger        Natronlauge,        versetzt          mit        20%        Kochsalz        und        dianotiert        in        der        Kälte     mit 7,7 Teilen     Natriumnitrit    und 50 Teilen  Salzsäure (d :

  l,16). Die     Diazoniumverbindung     wird     abfiltriert    und in     Anschlämmung    mit  11,0 Teilen     1.,3-Dioxy-benzol    in Gegenwart von  40 Teilen     Natriumcarbonat    gekuppelt.

   Den       Disazofarbstoff    säuert man mit 125 Teilen         Tetrazoverbindung    von     1-(4'-Arnino-benzoyl-          amino)-4-amino-benzol    einerseits mit 1     Mol     des     Disazofarbstoffes    der Formel    Salzsäure (d     :

  1,1.6)    aus, filtriert und löst ihn       in        Wasser        und        20        Teilen        30        %        iger        Natron-          lauge.    Durch Zugabe dieser Lösung zur       Tetrazoverbindung    aus     1.9,1.    Teilen     1-(4'-          Arnino-benzoylamino)-4-amino-benzol    wird in  schwach     lackmussaurer    Lösung das Zwischen  produkt hergestellt.

   Dann versetzt man mit  8,4 Teilen     3-Methyl-5-pyrazolon    in neutraler,  wässriger Lösung und anschliessend mit 7,2  Teilen     Natriumbicarbonat    in 144 Teilen Was  ser. Ist die Kupplung beendet, wird der Farb  stoff heiss     ausgesalzen,        abfiltriert    und ge  trocknet.  



  Als dunkles Pulver löst sich der Farb  stoff in Wasser und in     konz.    Schwefelsäure  mit brauner Farbe. Er färbt     Cellulosefasern     in braunen Tönen an, die mit Kupfersulfat  behandelt vor allem sehr gute Licht-, Wasch-,  Säure- und Schweissechtheit zeigen.



  <B> Additional patent </B> to main patent no. 282092. Process for the production of a copper-compatible tetrakisazo dye. \         Object. present patent is a method of making a copperable tetrakisazo dye. The process is characterized by the fact that one mole of
EMI0001.0006
    and on the other hand combined with 1 mole of 3-methyl-5-pyrazolone.



       1 -.) A nice tetrakisazo dye obtained is a dark powder and dissolves in water and conc. Sulfuric acid with a brown color.



  <I> Example: </I> 17.2 parts of 1-arrrinobenzene-3-sulfonic acid are dianotated with 6.9 parts of sodium nitrite in a known manner and coupled in the presence of 14.6 parts of 30% strength sodium hydroxide solution and 25 parts of sodium carbonate with 16.0 parts of 1-acetylamino-2-oxy-benzene. When the coupling is ready, the dye is saponified by heating with dilute sodium hydroxide solution, with,

   dilute sulfuric acid precipitated cold and filtered off. The dye is now dissolved in water and 17 parts of 30% strength sodium hydroxide solution, 20% sodium chloride is added and 7.7 parts of sodium nitrite and 50 parts of hydrochloric acid are added in the cold.

  l, 16). The diazonium compound is filtered off and coupled in suspension with 11.0 parts of 1, 3-dioxy-benzene in the presence of 40 parts of sodium carbonate.

   The disazo dye is acidified with 125 parts of the tetrazo compound of 1- (4'-amino-benzoyl-amino) -4-aminobenzene on the one hand with 1 mol of the disazo dye of the formula hydrochloric acid (d:

  1.1.6), filtered and dissolved in water and 20 parts of 30% sodium hydroxide solution. By adding this solution to the tetrazo compound from 1.9.1. Parts of 1- (4'-amino-benzoylamino) -4-aminobenzene are used to prepare the intermediate product in weakly lacquer acidic solution.

   8.4 parts of 3-methyl-5-pyrazolone in neutral, aqueous solution are then added, followed by 7.2 parts of sodium bicarbonate in 144 parts of water. Once the coupling has ended, the dye is salted out while hot, filtered off and dried.



  As a dark powder, the dye dissolves in water and in conc. Sulfuric acid with a brown color. It dyes cellulose fibers in brown tones which, when treated with copper sulphate, show very good fastness to light, washing, acids and perspiration.

 

Claims (1)

PATENTANSPRUCH Verfahren zur Herstellung eines kupfer baren Tetrakisazofarbstoffes, dadurch ge kennzeichnet, dass man 7. Mol. der Tetrazo-, verbindung von 1-(4'-Amino-benzoylamino)- 4-amino-benzol einerseits mit 1 Mol des Dis azofarbstoffes der Formel EMI0002.0004 und anderseits mit 1 Mo1 3-AZethyl-5-pyrazolon vereinigt. PATENT CLAIM Process for the preparation of a copper-ble tetrakisazo dye, characterized in that one 7. Mol. The tetrazo, compound of 1- (4'-amino-benzoylamino) -4-amino-benzene on the one hand with 1 mol of the disazo dye of the formula EMI0002.0004 and on the other hand combined with 1 mol of 3-AZethyl-5-pyrazolone. Der erhaltene neue Tetrakisazofarbstoff stellt ein dunkles Pulver dar und löst sich in Wasser und konz. Schwefelsäure mit. brau ner Farbe. The new tetrakisazo dye obtained is a dark powder and dissolves in water and conc. Sulfuric acid with. brown color.
CH285002D 1949-11-25 1949-11-25 Process for the preparation of a copper-compatible tetrakisazo dye. CH285002A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH285002T 1949-11-25
CH282092T 1949-11-25

Publications (1)

Publication Number Publication Date
CH285002A true CH285002A (en) 1952-08-15

Family

ID=25732149

Family Applications (1)

Application Number Title Priority Date Filing Date
CH285002D CH285002A (en) 1949-11-25 1949-11-25 Process for the preparation of a copper-compatible tetrakisazo dye.

Country Status (1)

Country Link
CH (1) CH285002A (en)

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