CH115466A - Process for the production of a new azo dye. - Google Patents

Process for the production of a new azo dye.

Info

Publication number
CH115466A
CH115466A CH115466DA CH115466A CH 115466 A CH115466 A CH 115466A CH 115466D A CH115466D A CH 115466DA CH 115466 A CH115466 A CH 115466A
Authority
CH
Switzerland
Prior art keywords
azo dye
production
new azo
new
plating
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH115466A publication Critical patent/CH115466A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds
    • 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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/10Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
    • C09B29/103Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the naphthalene series
    • 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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds
    • C09B45/16Monoazo compounds containing chromium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur     Herstellung    eines neuen     Azofarbstofes.       Es wurde gefunden, dass man einen neuen       Azofarbstoff    erhält, wenn man das     1-Oxy-          naphthalin-3,8-disulfamid    mit     diazotiertem        4-          Chlor-2-amino-l-oxybenzol    kuppelt. Der neue  Farbstoff bildet ein     schwärzlichbraunes    Pul  ver und färbt Wolle im essigsauren Bade in  Braunbordeaux Farbtönen, welche beim     Nach-          chromieren    rotblau, beim Nachkupfern vio  lett und echt werden.  



       Beispiel:     14,3 Teile     4-Chlor-2-amino-l-oxybenzol     werden in üblicher Weise     diazotiert    und bei  <B>5-10'</B> in eine Lösung von 30,2 Teilen     1-          Oxynaphthalin    - 3,8 -     disulfamid,    27 Teilen  30     %iger    Natronlauge, 10 Teilen Soda in 90  Teilen Wasser eingetragen. Man rührt bei    <B>10'</B> bis zur vollendeten Kupplung, verdünnt  mit 150 Teilen Wasser und giesst das Reak  tionsgemisch in 140 Teile einer 15     %igen    Salz  säure und salzt aus.



  Process for the preparation of a new azo dye. It has been found that a new azo dye is obtained when 1-oxynaphthalene-3,8-disulfamide is coupled with diazotized 4-chloro-2-amino-1-oxybenzene. The new dye forms a blackish-brown powder and dyes wool in an acetic acid bath in brown-burgundy shades, which become red-blue when chrome-plated, and purple and real when copper-plated.



       Example: 14.3 parts of 4-chloro-2-amino-1-oxybenzene are diazotized in the usual way and at <B> 5-10 </B> in a solution of 30.2 parts of 1-oxynaphthalene - 3.8 - Disulfamide, 27 parts of 30% sodium hydroxide solution, 10 parts of soda added to 90 parts of water. The mixture is stirred at <B> 10 '</B> until coupling is complete, diluted with 150 parts of water and the reaction mixture is poured into 140 parts of a 15% hydrochloric acid and salted out.

 

Claims (1)

PATEN TANSPRÜCII Verfahren zur Herstellung eines neuen Azofarbstoffes, dadurch gekennzeichnet, dass man das 1-Ogynaphthalin-3,8-disulfamid mit diazotiertem 4 - Chlor-2-amino - 1- oxybenzol kuppelt. Der neue Farbstoff bildet ein schwärzlichbraunes Pulver und färbt Wolle im essigsauren Bade in Braunbordeaux Farb tönen, welche beim Nachchromieren rotblau, beim Nachkupfern violett und echt werden. PATEN TANSPRÜCII Process for the preparation of a new azo dye, characterized in that 1-ogynaphthalene-3,8-disulfamide is coupled with diazotized 4-chloro-2-amino-1-oxybenzene. The new dye forms a blackish-brown powder and dyes wool in an acetic acid bath in brown-burgundy shades, which become red-blue when chrome-plating and purple and real when copper-plating.
CH115466D 1922-11-18 1924-04-20 Process for the production of a new azo dye. CH115466A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH101614T 1922-11-18
CH115466T 1924-04-20

Publications (1)

Publication Number Publication Date
CH115466A true CH115466A (en) 1926-06-16

Family

ID=25706020

Family Applications (1)

Application Number Title Priority Date Filing Date
CH115466D CH115466A (en) 1922-11-18 1924-04-20 Process for the production of a new azo dye.

Country Status (1)

Country Link
CH (1) CH115466A (en)

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