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CH285004A - 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
CH285004A
CH285004A CH285004DA CH285004A CH 285004 A CH285004 A CH 285004A CH 285004D A CH285004D A CH 285004DA CH 285004 A CH285004 A CH 285004A
Authority
CH
Switzerland
Prior art keywords
dye
parts
copper
compatible
preparation
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 CH285004A publication Critical patent/CH285004A/en

Links

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

Landscapes

  • 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 gekennzeichnet, dass man 1     Mol    der  
EMI0001.0004     
    und anderseits mit 1     Mol        3-Methy        1-5-pyrazolon     vereinigt.  



  Der erhaltene neue     Tetrakisazofarbstoff     stellt ein dunkles Pulver dar und löst sich in  Wasser und     konz.    Schwefelsäure mit brauner  Farbe.  



  <I>Beispiel:</I>  Man     diazotiert    30,3 Teile     2-Amino-naph-          thalin-4,8-disulfonsäure    mit 6,9 Teilen Na  triumnitrit in bekannter Weise und kuppelt       in        Anwesenheit        von        14,6        Teilen        30        %        iger        Na-          tronlauge    und 25 Teilen N     atriumcarbonat    mit  <B>16,0</B> Teilen     1-Acetylamino-2-oxy-benzol.    Ist die  Kupplung fertig,

   wird der Farbstoff durch  Erhitzen mit verdünnter Natronlauge verseift,  mit verdünnter Schwefelsäure kalt ausgefällt  und     abfiltriert.    Man löst nun den Farbstoff       in        Wasser        und        17        Teilen        30%iger        Natron-          lauge,        versetzt        mit        20%        Kochsalz        und        diazo-          tiert    in der Kälte mit 7,

  7 Teilen Natrium  nitrit und 50 Teilen Salzsäure (d :1.,16). Die       Diazoniumverbindung    wird     abfiltriert    und in         Tetrazoverbindung    von     1-(4'-Amino-benzoyl)-          4-amino-benzol    einerseits mit 1.     Mol    des Dis  azofarbstoffes der Formel         Anschlämmung    mit<B>11,0</B> Teilen     1,3-Dioxy-ben-          zol    in Gegenwart von 40 Teilen     Natrium-          carbonat    gekuppelt.

   Den     Disazofarbstoff     säuert man mit 125 Teilen Salzsäure<B>(d:</B> 1,16)  aus, filtriert und löst     ihn    in Wasser und       20        Teilen        30        %        iger        Natronlauge.        Durch        Zu-          gabe    dieser Lösung zur     Tetrazoverbindung    aus  19,1 Teilen 1 -     (4'-Amino-benzoylamino)    -4  amino-benzol wird in schwach     lackmussaurer     Lösung das Zwischenprodukt     hergestellt.    Dann  versetzt man mit 8,

  4 Teilen     3-hlethyl-5-pyr-          azolon    in neutraler, wässriger     Lösung    und an  schliessend mit 7,2 Teilen     Natriumbicarbonat     in 144 Teilen Wasser. Ist die Kupplung be  endet, wird der Farbstoff heiss     ausgesalzen,          abfiltriert    und getrocknet.  



  Als dunkles Pulver löst sich der Farbstoff  in Wasser und in     konz.    Schwefelsäure mit  brauner Farbe. Er färbt.     Cellulosefasern    in  braunen Tönen an, die mit Kupfersulfat be  handelt 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. The present patent relates to a process for the preparation of a copper-compatible tetrakisazo dye. The process is characterized in that one mole of the
EMI0001.0004
    and on the other hand combined with 1 mol of 3-methyl 1-5-pyrazolone.



  The new tetrakisazo dye obtained is a dark powder and dissolves in water and conc. Sulfuric acid with a brown color.



  <I> Example: </I> 30.3 parts of 2-amino-naphthalene-4,8-disulfonic acid are diazotized 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. Is the clutch ready,

   the dye is saponified by heating with dilute sodium hydroxide solution, precipitated cold with dilute sulfuric acid and filtered off. The dye is now dissolved in water and 17 parts of 30% sodium hydroxide solution, mixed with 20% sodium chloride and diazotized in the cold with 7,

  7 parts of sodium nitrite and 50 parts of hydrochloric acid (d: 1st, 16). The diazonium compound is filtered off and the tetrazo compound of 1- (4'-aminobenzoyl) -4-aminobenzene on the one hand with 1. mol of the disazo dye of the formula slurry with 11.0 parts 1.3 -Dioxy-benzene coupled in the presence of 40 parts of sodium carbonate.

   The disazo dye is acidified with 125 parts of hydrochloric acid (d: 1.16), filtered and dissolved in water and 20 parts of 30% strength sodium hydroxide solution. By adding this solution to the tetrazo compound of 19.1 parts of 1- (4'-amino-benzoylamino) -4-amino-benzene, the intermediate product is prepared in a weakly lacquer acidic solution. Then add 8,

  4 parts of 3-methyl-5-pyrazolone in neutral, aqueous solution and then with 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. He colors. Cellulose fibers in brown tones, which are treated with copper sulfate and especially 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 1 Mol der Tetrazover- EMI0002.0003 und anderseits mit 1 Mol 3-Methyl-5-pyrazolon vereinigt. PATENT CLAIM: Process for the production of a copper-ble tetrakisazo dye, characterized in this. that one mole of the tetrazo EMI0002.0003 and on the other hand combined with 1 mole of 3-methyl-5-pyrazolone. Der erhaltene neue Tetrakisazofarbstoff stellt ein dunkles Pulver dar und löst sich in bindung von 1- (4'-Amino-benzoyl)-4-amino- benzol einerseits mit 7. Mol des Disazofarb- stoffes der Formel Wasser und konz. Schwefelsäure mit brauner Farbe. The new tetrakisazo dye obtained is a dark powder and dissolves in the bond of 1- (4'-amino-benzoyl) -4-aminobenzene on the one hand with 7th mol of the disazo dye of the formula water and conc. Sulfuric acid with a brown color.
CH285004D 1949-11-25 1949-11-25 Process for the preparation of a copper-compatible tetrakisazo dye. CH285004A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH282092T 1949-11-25
CH285004T 1949-11-25

Publications (1)

Publication Number Publication Date
CH285004A true CH285004A (en) 1952-08-15

Family

ID=25732151

Family Applications (1)

Application Number Title Priority Date Filing Date
CH285004D CH285004A (en) 1949-11-25 1949-11-25 Process for the preparation of a copper-compatible tetrakisazo dye.

Country Status (1)

Country Link
CH (1) CH285004A (en)

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