[go: up one dir, main page]

CH220222A - Process for the production of a vat dye. - Google Patents

Process for the production of a vat dye.

Info

Publication number
CH220222A
CH220222A CH220222DA CH220222A CH 220222 A CH220222 A CH 220222A CH 220222D A CH220222D A CH 220222DA CH 220222 A CH220222 A CH 220222A
Authority
CH
Switzerland
Prior art keywords
methoxy
vat dye
production
good
reactive
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellsc Farbenindustrie
Original Assignee
Ig Farbenindustrie Ag
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 Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Publication of CH220222A publication Critical patent/CH220222A/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
    • C09B7/00Indigoid dyes
    • C09B7/10Bis-thionapthene indigos

Landscapes

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

Description

       

  Verfahren zur Herstellung eines     Küpenfarbstoffes.       Es wurde gefunden, dass man wertvolle,  neue, unsymmetrische     Küpenfarbstoffe    erhält,  wenn man     6-Methoxy-4-trifluormethyl-3-oxy-          thionaphthen    mit einem reaktionsfähigen     2-          Derivat    des     6-Methoxy-2.3-diketodihydrothio-          naphthenchinons    oder des     4-Methyl-6-chlor-          2.3-diketodihydrothionaphthenchinons    konden  siert.

   Die neuen Farbstoffe werden durch fol  gende allgemeine Formel gekennzeichnet  
EMI0001.0011     
    worin X eine der folgenden Atomgruppen  bedeutet:  
EMI0001.0012     
    Die neuen     Farbstoffe    zeichnen sich neben  guten bis sehr guten Echtheitseigenschaften  vor allem durch ihre lebhaften, leuchtenden  Scharlachtöne aus und sind sowohl als     Färbe-          wie        Druckfarbstoffe    von hervorragender Be  deutung.  



  Gegenüber den in der amerikanischen  Patentschrift 2061186 beschriebenen unsym  metrischen     Thioindigofarbstoffen    weisen die       neuenFarbstoffe    grössere Ausgiebigkeit, einen  klareren Farbton und bessere Echtheitseigen  schaften auf.  



  Das als     Ausgangsstoff    zur Verwendung  kommende     6-Methoxy-4-trifluormethyl-3-oxy-          thionaphthen    kann in der Weise erhalten  werden, dass man die in     2-Stellung    durch  eine     Carboxyl-,        Carbonamid-    oder     Cyangruppe     substituierte 3 -     Tri$uormethyl-    5     -methoxy-l-          thioglycolsäure    den üblichen Kondensations  methoden     unterwirft.     



  Gegenstand des     vorliegenden    Patentes ist  ein Verfahren     zur    Herstellung eines Küpen-      Farbstoffes, welches dadurch gekennzeichnet  ist, dass man     6-13lethoxy-4-trifluormethyl-3-          oxythionaphthen    mit einem reaktionsfähigen       2-Derivat    des     6-AZethoxy-2.3-diketodihydro-          thionaphthenchinons    kondensiert. Der neue       Küpenfarbstoff    löst sich in Schwefelsäure in  der Wärme mit blauer Farbe und färbt  Baumwolle in sehr schönen, lebhaften,     gelb-          stichigen    Scharlachtönen von guten bis sehr  guten Echtheitseigenschaften.

      <I>Beispiel:</I>  12,4 Gewichtsteile     6-Metlioxy-4-trifluor-          methyl-3-oxytliioriaplithen    werden in 300 Ge  wichtsteilen Eisessig mit 16 Gewichtsteilen  6 -     Metlioxy    - 2.3 -     diketodihydrothionaphthen        -          cliinoii-2-(p-dimetliylamino)-anil    10 Stunden  bei 70   C erhitzt. Die Umsetzung geht nach  folgendem Schema vor sich  
EMI0002.0015     
    Der nach dem Erkalten abgesaugte und  neutral gewaschene     Farbstoff    löst sich in  Schwefelsäure in der Wärme mit blauer  Farbe und färbt Baumwolle in sehr schönen,  lebhaften,     gelbstichigen    Scharlachtönen von  guten bis sehr guten Echtheitseigenschaften.



  Process for the production of a vat dye. It has been found that valuable, new, asymmetrical vat dyes are obtained if 6-methoxy-4-trifluoromethyl-3-oxy-thionaphthene is used with a reactive 2-derivative of 6-methoxy-2,3-diketodihydrothionnaphthenquinone or 4-methyl -6-chloro- 2.3-diketodihydrothionaphthenquinones condensed.

   The new dyes are characterized by the following general formula
EMI0001.0011
    where X is one of the following atomic groups:
EMI0001.0012
    In addition to good to very good fastness properties, the new dyes are distinguished above all by their lively, luminous scarlet tones and are of outstanding importance both as dyeing and printing dyes.



  Compared to the unsymmetrical thioindigo dyes described in the American patent specification 2061186, the new dyes have greater yield, a clearer shade and better fastness properties.



  The 6-methoxy-4-trifluoromethyl-3-oxy-thionaphthene used as starting material can be obtained in such a way that the 3-tri-uormethyl-5 substituted in the 2-position by a carboxyl, carbonamide or cyano group -methoxy-l-thioglycolic acid subjected to the usual condensation methods.



  The subject of the present patent is a process for the preparation of a vat dye, which is characterized in that 6-13lethoxy-4-trifluoromethyl-3-oxythionaphthene is condensed with a reactive 2-derivative of 6-AZethoxy-2,3-diketodihydro- thionaphthenchinons. The new vat dye dissolves in sulfuric acid in the warmth with a blue color and dyes cotton in very beautiful, lively, yellow-tinged scarlet shades with good to very good fastness properties.

      <I> Example: </I> 12.4 parts by weight of 6-metlioxy-4-trifluoromethyl-3-oxytliioriaplithen are mixed in 300 parts by weight of glacial acetic acid with 16 parts by weight of 6 - metlioxy - 2.3 - diketodihydrothionaphthen - cliinoii-2- (p- dimetliylamino) anil heated at 70 C for 10 hours. The implementation proceeds according to the following scheme
EMI0002.0015
    The dye, which is sucked off after cooling and washed neutral, dissolves in sulfuric acid in the warmth with a blue color and dyes cotton in very beautiful, lively, yellowish scarlet shades with good to very good fastness properties.


    

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Küpen- farbstoffes, dadurch gekennzeichnet, dass man 6-blethoxy-4-trifluormethyl-3-oyytliionaplitlien mit einem reaktionsfähigen 2-Derivat des 6 - Methoxy - 2.3 - diketodihydrothionaphthen - chinons kondensiert. Der gebildete Küpenfarbstoff löst sich in Schwefelsäure in der Wärme mit blauer Farbe und färbt Baumwolle in sehr schönen, leb haften, gelbatichigen Scharlachtönen von guten bis sehr guten Echtheitseigenschaften. PATENT CLAIM: Process for the production of a vat dye, characterized in that 6-methoxy-4-trifluoromethyl-3-oyytliionaplitlien is condensed with a reactive 2-derivative of 6 - methoxy - 2.3 - diketodihydrothionaphthen - quinone. The vat dye formed dissolves in sulfuric acid in the warmth with a blue color and dyes cotton in very beautiful, lively, yellowish scarlet shades with good to very good fastness properties. UNTERANSPRUCH: Verfahren nach Patentanspruch, dadurch gekennzeichnet, dass man als reaktionsfähiges 2-Derivat des 6-Metlioxy-2.3-diketodihydro- thionaphtlienchinons 6-Methoxy-2.3-diketodi hydrotliioriaplithenchinon-2-(p-dimethylamino)- anil verwendet. SUBSTANTIAL CLAIM: Process according to claim, characterized in that 6-methoxy-2,3-diketodi hydrotliioriaplithenquinone-2- (p-dimethylamino) anil is used as the reactive 2-derivative of 6-metlioxy-2,3-diketodihydthionaphtlienchinons.
CH220222D 1940-02-15 1940-12-05 Process for the production of a vat dye. CH220222A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE220222X 1940-02-15

Publications (1)

Publication Number Publication Date
CH220222A true CH220222A (en) 1942-03-31

Family

ID=5833311

Family Applications (1)

Application Number Title Priority Date Filing Date
CH220222D CH220222A (en) 1940-02-15 1940-12-05 Process for the production of a vat dye.

Country Status (1)

Country Link
CH (1) CH220222A (en)

Similar Documents

Publication Publication Date Title
CH220222A (en) Process for the production of a vat dye.
DE745417C (en) Process for the preparation of asymmetrical thioindigo dyes
DE675196C (en) Process for dyeing acetate rayon
AT33317B (en) Process for the preparation of mono- and dibromo derivatives of indigo.
CH222473A (en) Process for the production of a vat dye.
DE609119C (en) Process for the production of Kuepen dyes
DE536294C (en) Process for the preparation of Kuepen dyes of the anthraquinone series
DE703065C (en) Method of dyeing wool
CH163280A (en) Process for the production of a new vat dye.
CH289993A (en) Process for the preparation of an anthraquinone dye.
CH222154A (en) Process for the preparation of a new dye of the anthraquinone series.
CH197184A (en) Process for the production of a sulfur dye.
CH269393A (en) Process for the preparation of a vivid acid dye of the anthraquinone series.
CH155459A (en) Process for the production of an indigoid vat dye.
CH176239A (en) Process for the preparation of an oxazine dye.
CH164443A (en) Process for the preparation of a nitrogenous anthraquinone derivative.
CH173984A (en) Process for the production of a new sulfur dye.
CH217980A (en) Process for the preparation of a new anthraquinone dye.
CH213191A (en) Process for the production of a vat dye of the anthraquinone series.
CH176238A (en) Process for the preparation of an oxazine dye.
CH175252A (en) Process for the preparation of an anthraquinone dye.
CH217979A (en) Process for the preparation of a new anthraquinone dye.
CH173745A (en) Process for the preparation of an oxazine dye.
CH265737A (en) Process for the preparation of a water-soluble dye of the naphthoquinone series.
CH165055A (en) Process for the production of a new vat dye.