CH249024A - Process for the preparation of an ester type azo dye derivative. - Google Patents

Process for the preparation of an ester type azo dye derivative.

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Publication number
CH249024A
CH249024A CH249024DA CH249024A CH 249024 A CH249024 A CH 249024A CH 249024D A CH249024D A CH 249024DA CH 249024 A CH249024 A CH 249024A
Authority
CH
Switzerland
Prior art keywords
preparation
azo dye
dye
ester type
dye derivative
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 CH249024A publication Critical patent/CH249024A/en

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Description

  

  Verfahren zur Herstellung eines     esterartigen        Azofarbatoffderivates.       Gegenstand des vorliegenden Zusatz  patentes ist ein Verfahren zur     Herstellung     eines     esterartigen    Derivates eines<B>0,0</B>     -Dioxy-          azofa-rbstoffes,    dadurch     gekennzeichnet,    dass  der     Azofarbstoff    aus     diazotiertem        1-Oxy-2-          a.mino-5-nitrobenzol    und     1-Oxy-5,

  8-dichlor-          naphtaIin    in Gegenwart von     Pyridin    mit       Benzoesäure-3-sulfochlorid    verestert wird.  



  Das neue     Farbstoffderivat    bildet nach  dem Aufarbeiten und Trocknen ein gelb  braunes, wasserlösliches Pulver. Es färbt       -rolle    nach dem     Einbadverfahren        in    Gegen  wart chromabgebender Mittel in     blaugrünen     Tönen.  



  <I>Beispiel:</I>  62 Teile     Benzoesäure-3-sulfochlorid    wer  den in 300 Teilen     Pyridin    bei 50-60  ge  löst. Bei 40-50  werden 38 Teile des     Azo-          farbstoffes    aus     diazotiertem        1-Oxy-2-amino-          5-nitrobenzol    und     1-Oxy-5,8-dichlornaphtalin     unter gutem Rühren zugegeben. Durch  Probeentnahme kann die     Veresterung    ver  folgt werden. Dieselbe     ist    beendet, wenn  eine Probe beim Versetzen mit Wasser keine    Fällung mehr gibt.

   Dann wird das Reak  tionsgemisch in 800 Teilen Wasser aufge  nommen, mit 200 Teilen Salzsäure bis zur  schwach kongosauren     Reaktion    versetzt und  der     Farbstoffester        abgenutscht.    Der     Press-          kuchen    wird nochmals in     etwa    500 Teilen  Wasser     verrührt,    nach Zusatz von 50 Teilen       Natriumchlorid    das     Farbstoffderivat        abfil-          triert    und im Vakuum getrocknet.



  Process for the preparation of an ester-like azo carbate derivative. The subject of the present additional patent is a process for the production of an ester-like derivative of a <B> 0,0 </B> -Dioxy- azo dye, characterized in that the azo dye is made from diazotized 1-oxy-2-a.mino-5 -nitrobenzene and 1-oxy-5,

  8-dichloronaphthalene is esterified with benzoic acid-3-sulfochloride in the presence of pyridine.



  The new dye derivative forms a yellow-brown, water-soluble powder after working up and drying. It colors-Rolle in blue-green tones using the single-bath process in the presence of chromium-releasing agents.



  <I> Example: </I> 62 parts of benzoic acid 3-sulfochloride are dissolved in 300 parts of pyridine at 50-60 ge. At 40-50, 38 parts of the azo dye from diazotized 1-oxy-2-amino-5-nitrobenzene and 1-oxy-5,8-dichloronaphthalene are added with thorough stirring. The esterification can be followed by taking a sample. This is over when a sample no longer gives any precipitation when it is mixed with water.

   Then the reaction mixture is taken up in 800 parts of water, treated with 200 parts of hydrochloric acid until the reaction is weakly Congo acidic and the dye ester is suction filtered. The press cake is again stirred in about 500 parts of water, and after the addition of 50 parts of sodium chloride, the dye derivative is filtered off and dried in vacuo.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines ester- artigen Derivates eines o,ö -Dioxyazofarb- stoffes, dadurch gekennzeichnet, da.ss der Azofarbstoff aus diazotiertem 1 - Oxy - 2 amino-5-nitrobenzol und 1-Oxy-5, PATENT CLAIM: Process for the preparation of an ester-like derivative of an o, ö -dioxyazo dye, characterized in that the azo dye from diazotized 1-oxy-2 amino-5-nitrobenzene and 1-oxy-5, 8-dichlor- naphtalin in Gegenwart von Pyridin mit Benzoesäure-3-sulfochlorid verestert wird. Das neue Farbstoffderivat bildet nach dem Aufarbeiten und Trocknen ein gelbbrau nes, wasserlösliches Pulver. Es färbt Wolle nach dem Einbadverfahren in Gegenwart chromabgebender Mittel in blaugrünen Tönen. 8-dichloronaphthalene is esterified with benzoic acid-3-sulfochloride in the presence of pyridine. After working up and drying, the new dye derivative forms a yellow-brown, water-soluble powder. It dyes wool by the single bath process in the presence of chromium-releasing agents in blue-green shades.
CH249024D 1944-10-06 1944-10-06 Process for the preparation of an ester type azo dye derivative. CH249024A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH249024T 1944-10-06
CH244049T 1945-08-22

Publications (1)

Publication Number Publication Date
CH249024A true CH249024A (en) 1947-05-31

Family

ID=25728878

Family Applications (1)

Application Number Title Priority Date Filing Date
CH249024D CH249024A (en) 1944-10-06 1944-10-06 Process for the preparation of an ester type azo dye derivative.

Country Status (1)

Country Link
CH (1) CH249024A (en)

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