CH200063A - Process for the preparation of an azo dye. - Google Patents

Process for the preparation of an azo dye.

Info

Publication number
CH200063A
CH200063A CH200063DA CH200063A CH 200063 A CH200063 A CH 200063A CH 200063D A CH200063D A CH 200063DA CH 200063 A CH200063 A CH 200063A
Authority
CH
Switzerland
Prior art keywords
azo dye
preparation
dye
purple
nitrobenzene
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 CH200063A publication Critical patent/CH200063A/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/06Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08Amino benzenes
    • C09B29/0801Amino benzenes containing acid groups, e.g. COOH, SO3H, PO3H2, OSO3H, OPO3H2; SO2NHSO2R or salts thereof, R being hydrocarbonyls
    • C09B29/0803Amino benzenes containing acid groups, e.g. COOH, SO3H, PO3H2, OSO3H, OPO3H2; SO2NHSO2R or salts thereof, R being hydrocarbonyls containing SO3H, OSO3H
    • 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
    • C09B29/06Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08Amino benzenes

Landscapes

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

Description

  

  Verfahren zur Herstellung eines     Azofarbstoffes.       Es wurde gefunden, dass man einen     Azo-          farbstoff    erhält, wenn man die     Diazoverbin-          dung    des     1-Amino-4-nitrobenzol-2-methylsul-          fons    mit     (2-Methoxy-5-methyl-2'-sulfonsäure-          4'    -     chloracetylamirio)    - N -     diphenylamin    der  Formel  
EMI0001.0012     
    vereinigt.

   Der neue Farbstoff bildet ein dunk  les Pulver, das sich in Wasser mit violetter  Farbe löst und das Wolle und Seide aus  saurem Bade in     violettblauen    Tönen färbt.  <I>Beispiel:</I>  216 Teile     1-Amino-4-nitrobenzol-2-methyl-          sulfon    werden     diazotiert    und in die mineral  saure Lösung dieser     Diazoverbindung    die Lö  sung des     Natriumsalzes    aus 384 Teilen (2       Methoxy-5-methyl-2'-sulfonsäure-4'-chlorace-          tylamino)-N-diphenylamin    eingetragen.

   Nach  dem die     Farbstoffbildung    beendet ist, wird       abfiltriert,    der Farbstoff in Wasser suspen-         diert    und durch Verrühren mit einem Alkali  neutral gestellt. Der Farbstoff wird eventuell  durch Zusatz eines Salzes ausgeschieden, ab  filtriert und getrocknet.



  Process for the preparation of an azo dye. It has been found that an azo dye is obtained if the diazo compound of 1-amino-4-nitrobenzene-2-methylsulfone is used with (2-methoxy-5-methyl-2'-sulfonic acid-4 '- chloracetylamirio) - N - diphenylamine of the formula
EMI0001.0012
    united.

   The new dye forms a dark powder that dissolves in water with a purple color and dyes the wool and silk from an acid bath in purple-blue tones. <I> Example: </I> 216 parts of 1-amino-4-nitrobenzene-2-methyl sulfone are diazotized and the solution of the sodium salt of 384 parts (2 methoxy-5-methyl- 2'-sulfonic acid-4'-chloroacetylamino) -N-diphenylamine entered.

   After the formation of the dye has ended, it is filtered off, the dye is suspended in water and neutralized by stirring with an alkali. The dye is possibly precipitated by adding a salt, filtered off and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Azofarb- stoffes, dadurch gekennzeichnet, dass man die Diazoverbindung des 1-Amino-4-nitrobenzol-2- methylsulfons mit dem (2-Methoxy-5-metbyl- 2'- sulfonsäure - 4'- chloracetylamino)-N-diphe- nvlamin der Formel EMI0001.0035 vereinigt. PATENT CLAIM: Process for the production of an azo dye, characterized in that the diazo compound of 1-amino-4-nitrobenzene-2-methylsulfone is mixed with (2-methoxy-5-metbyl-2'-sulfonic acid - 4'-chloroacetylamino) -N-diphe- nvlamin of the formula EMI0001.0035 united. Der neue Farbstoff bildet ein dunk les Pulver, das sich in Wasser mit violetter Farbe löst und das Wolle und Seide aus saurem Bade in violettblauen Tönen färbt. The new dye forms a dark powder that dissolves in water with a purple color and dyes the wool and silk from an acid bath in purple-blue tones.
CH200063D 1938-11-09 1937-03-15 Process for the preparation of an azo dye. CH200063A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH200063T 1938-11-09

Publications (1)

Publication Number Publication Date
CH200063A true CH200063A (en) 1938-09-30

Family

ID=4442148

Family Applications (1)

Application Number Title Priority Date Filing Date
CH200063D CH200063A (en) 1938-11-09 1937-03-15 Process for the preparation of an azo dye.

Country Status (1)

Country Link
CH (1) CH200063A (en)

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