[go: up one dir, main page]

CH301816A - Process for the preparation of a monoazo dye. - Google Patents

Process for the preparation of a monoazo dye.

Info

Publication number
CH301816A
CH301816A CH301816DA CH301816A CH 301816 A CH301816 A CH 301816A CH 301816D A CH301816D A CH 301816DA CH 301816 A CH301816 A CH 301816A
Authority
CH
Switzerland
Prior art keywords
dye
tones
monoazo dye
bath
preparation
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellschaft Ciba
Original Assignee
Ciba 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 Ciba Geigy filed Critical Ciba Geigy
Publication of CH301816A publication Critical patent/CH301816A/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
    • C09B45/16Monoazo compounds containing chromium

Landscapes

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

Description

  

  Verfahren zur Herstellung     eines        Monoazofarbstoffes.       Es wurde gefunden, dass man zu einem  neuen, wertvollen     Monoazofarbstoff    gelangt,       wenn    man     1-Phenylamino-S-oxynaphthalin-4-          sulfonsäure    mit     diazotiertein        6--,\Titro-2-aniino-          1-oxybenzol-4-m,ethylsulfon    vereinigt.  



  Der neue Farbstoff bildet ein dunkles Pul  ver, das sieh in Wasser mit blauer, in kon  zentrierter Schwefelsäure mit bordeauxroter  Farbe löst und Wolle aus essigsaurem Bade  in blauen Tönen färbt, die durch     Nachehro-          inieren    in ein sehr echtes Grün übergehen..  Der Farbstoff eignet sich auch vorzüglich zum  Färben nach dem     Einbadchromierverfahren,     wobei ebenfalls echte grüne Töne erhalten  werden,  Die Dianotierung des     6-Nitro-2-amino-l-          oxybenzol-4-methylsitlfons    kann nach an. sich  bekannten Methoden erfolgen, zum Beispiel  mittels     Natriumnitrit    und Salzsäure.  



  Die Kupplung wird beim vorliegenden  Verfahren mit Vorteil in alkalischem Medium       durchgeführt.     



  <I>Beispiel:</I>  23,2 Teile     6-Nitro-2-amina-l-oxybenzol-4-          metliylsulfon    werden in üblicher Weise in salz  saurer Lösung mit     Natriumnitrit    dianotiert.  Die mit     Natriumcarbonat    neutralisierte Di-         azoverbindung    vereinigt man mit einer mit  Eis abgekühlten Lösung, hergestellt aus  33 Teilen     1-Phenylamino-S-oxynaphthalin-4-          sulfonsä.ure,    50     Volumteilen    Wasser,

   50     Vo-          lumteilen        2n    -     Natriumhy        droxydlösung    und  50     Volumteilen    einer     15prozentigen    Natrium  carbonatlösung. Nach beendeter Kupplung  wird der abgeschiedene Farbstoff     abfiltriert,     mit verdünnter     Natriumchloridlösung        gewa-          sehen    und getrocknet.



  Process for the preparation of a monoazo dye. It has been found that a new, valuable monoazo dye is obtained if 1-phenylamino-S-oxynaphthalene-4-sulfonic acid is combined with diazotized 6 -, \ titro-2-aniino-1-oxybenzene-4-m, ethyl sulfone .



  The new dye forms a dark powder that dissolves in water with a blue color, in concentrated sulfuric acid it dissolves with a burgundy red color, and dyes wool from an acetic acid bath in blue tones, which turn into a very real green through subsequent ironing. The dye is suitable is also excellent for dyeing by the single-bath chromium plating process, which also gives real green tones. The dianotation of 6-nitro-2-amino-l-oxybenzene-4-methylsitlfons can also known methods are carried out, for example using sodium nitrite and hydrochloric acid.



  In the present process, the coupling is advantageously carried out in an alkaline medium.



  <I> Example: </I> 23.2 parts of 6-nitro-2-amina-1-oxybenzene-4-methylsulfone are dianotized with sodium nitrite in the usual way in a salt-acidic solution. The diazo compound neutralized with sodium carbonate is combined with a solution cooled with ice, prepared from 33 parts of 1-phenylamino-S-oxynaphthalene-4-sulfonic acid, 50 parts by volume of water,

   50 parts by volume of 2N sodium hydroxide solution and 50 parts by volume of a 15 percent sodium carbonate solution. After the coupling has ended, the deposited dye is filtered off, washed with dilute sodium chloride solution and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Mono- azofarbstoffes, dadurch gekennzeichnet, dass man 1-Phen@Tlamino-8-oxynaphthalin-4-sulfon- säure mit dianotiertem 6-@Titro 2-amino-l-oxy- benzol-4-methylsulfon vereinigt. Der neue Farbstoff bildet ein dunkles Pulver, das sich in Wasser mit blauer, in konzentrierter Schwefelsäure mit bordeaux roter Farbe löst und: Wolle aus essigsaurem Bade in blauen Tönen färbt, die durch Nach- chromieren in ein sehr echtes Grün übergehen. Claim: Process for the production of a monoazo dye, characterized in that 1-Phen @ Tlamino-8-oxynaphthalene-4-sulfonic acid is combined with dianotated 6- @ Titro 2-amino-1-oxybenzene-4-methylsulfone . The new dye forms a dark powder that dissolves in water with a blue color, and in concentrated sulfuric acid with a burgundy red color. It dyes wool from an acetic acid bath in blue tones that turn into a very real green when chromium-plated. Der Farbstoff eignet sich auch vorzüglich zum Färben nach dem Einbadchromierverfah- ren, wobei ebenfalls echte _-grüne Töne er halten werden. The dye is also ideally suited for dyeing using the single-bath chrome plating process, which also gives real _-green tones.
CH301816D 1952-03-19 1952-03-19 Process for the preparation of a monoazo dye. CH301816A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH301816T 1952-03-19

Publications (1)

Publication Number Publication Date
CH301816A true CH301816A (en) 1954-09-30

Family

ID=4491173

Family Applications (1)

Application Number Title Priority Date Filing Date
CH301816D CH301816A (en) 1952-03-19 1952-03-19 Process for the preparation of a monoazo dye.

Country Status (1)

Country Link
CH (1) CH301816A (en)

Similar Documents

Publication Publication Date Title
CH301816A (en) Process for the preparation of a monoazo dye.
CH304607A (en) Process for the preparation of a monoazo dye.
CH307858A (en) Process for the preparation of a monoazo dye.
CH261368A (en) Process for the preparation of a monoazo dye.
CH263499A (en) Process for the preparation of an azo dye.
CH275801A (en) Process for the preparation of a metallizable monoazo dye.
CH266278A (en) Process for the preparation of an o, o&#39;-dioxyazo dye.
CH200370A (en) Process for the preparation of a chromable o-oxydisazo dye.
CH263498A (en) Process for the preparation of an azo dye.
CH267274A (en) Process for the preparation of a monoazo dye.
CH267276A (en) Process for the preparation of a monoazo dye.
CH266023A (en) Process for the preparation of a monoazo dye.
CH282258A (en) Process for the preparation of a monoazo dye.
CH261058A (en) Process for the preparation of a polyazo dye.
CH266025A (en) Process for the preparation of a monoazo dye.
CH257030A (en) Process for the production of a metallizable azo dye.
CH292298A (en) Process for the preparation of a monoazo dye of the pyrazolone series.
CH257026A (en) Process for the production of a metallizable azo dye.
CH290493A (en) Process for the preparation of an azo dye.
CH267277A (en) Process for the preparation of a monoazo dye.
CH258758A (en) Process for the preparation of an azo dye.
CH257031A (en) Process for the production of a metallizable azo dye.
CH263496A (en) Process for the preparation of an azo dye.
CH266022A (en) Process for the preparation of a monoazo dye.
CH268397A (en) Process for the preparation of an azo dye.