CH149421A - Process for the preparation of a vat dye. - Google Patents

Process for the preparation of a vat dye.

Info

Publication number
CH149421A
CH149421A CH149421DA CH149421A CH 149421 A CH149421 A CH 149421A CH 149421D A CH149421D A CH 149421DA CH 149421 A CH149421 A CH 149421A
Authority
CH
Switzerland
Prior art keywords
methyl
preparation
vat dye
anil
dye
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 CH149421A publication Critical patent/CH149421A/en

Links

Landscapes

  • Coloring (AREA)

Description

  

  Verfahren zur Darstellung eines     Küpenfarbstoffes.       Es wurde gefunden, dass man wertvolle,  neue unsymmetrische     Küpenfarbstoffe    er  hält, wenn man reaktionsfähige     2-Derivate     der     4-Alkyl-5.7-dihalogen-2.3-diketo-tlihy-          drothionaphthenchinone        mit        Oxythionaph-          thenen,    gegebenenfalls in Anwesenheit von  Verdünnungsmitteln, kondensiert.

   Von be  sonderem Interesse sind die Farbstoffe, die  durch     Kondensation    mit     4-Methyl-6-halogen-          oder    4.     6-Dimethyloxythionaphthen    erhalten       werden.     



  Die neuen Farbstoffe zeichnen sich neben  einer guten Licht-, Wasch- und     Bäuchecht-          heit    vor allem durch ihre lebhaften leuchten  den roten Farbtöne aus und sind sowohl als  Färbe- wie Druckstoffe praktisch von hervor  ragender Bedeutung.  



  Der aus dem     2-Anil    des     4-Methyl-5    . 7  dichlor-2.3-diketodihydrothionaphthen ent  stehende symmetrische 4 . 4' -     Dimethyl-.     5. 5'. 7 .     7'-tetrachlorthioindigo    ist bekannt  (D. R. P. Nr. 241910,     $l.    22e). Er färbt ein    Rotviolett, das jedoch nur ungenügende  Lichtechtheit besitzt.  



  Gegenstand des vorliegendes Patentes ist  ein Verfahren zur Darstellung von 4.     4'-Di-          methyl-5    . 7 .     6'-trichlorthioincligo,        welcliN     dadurch gekennzeichnet ist. dass     4-Methyl-          5    .     7-diehlor-2    .     3-diketodihydrothionaphthen-          chinon-2-(p-dimethylamino)-anil    mit     4-Me-          thyl-6-ehlor-3-oxythionaphthen    kondensiert  wird.  



       Beispiel:     36,5 Gewichtsteile     4-Methyl-5.        7-dichlor-          2    . 3 -     diketodihydrothionaphthenchinon-        2-(p-          dimethylamino)-anil    werden mit 20     C@        e-          wichtsteilen        4-Methyl-6-chlor-3-oxythionaph-          then    in 500 Gewichtsteilen Eisessig 10 Stun  den bei 70   C erhitzt.

   Der nach dem Erkal  ten abgesaugte und neutral gewaschene Farb  stoff färbt Baumwolle in sehr schönen, leb  haften, blaustichigen     Rosatönen    von guter  Licht-, Wasch- und     Bäuchechtheit    an.



  Process for the preparation of a vat dye. It has been found that valuable, new unsymmetrical vat dyes are obtained if reactive 2-derivatives of 4-alkyl-5.7-dihalo-2,3-diketo-thihydrothionaphthenquinones are condensed with oxythionaphthenes, optionally in the presence of diluents.

   Of particular interest are the dyes which are obtained by condensation with 4-methyl-6-halogen- or 4-6-dimethyloxythionaphthene.



  In addition to good lightfastness, washfastness and tummy fastness, the new dyes are characterized above all by their lively, glowing red shades and are of outstanding importance in practice both as dyes and printing materials.



  The one from the 2-anil of the 4-methyl-5. 7 dichloro-2,3-diketodihydrothionaphthene symmetrical 4. 4 '- dimethyl. 5. 5 '. 7th 7'-tetrachlorthioindigo is known (D.R.P. No. 241910, $ 1.22e). It colors a red-violet, which, however, has insufficient lightfastness.



  The subject of the present patent is a process for the preparation of 4,4'-dimethyl-5. 7th 6'-trichlorthioincligo, which is characterized. that 4-methyl- 5. 7-diehlor-2. 3-diketodihydrothionaphthen-quinon-2- (p-dimethylamino) -anil is condensed with 4-methyl-6-chloro-3-oxythionaphthene.



       Example: 36.5 parts by weight of 4-methyl-5. 7-dichloro- 2. 3 - diketodihydrothionaphthenchinon- 2- (p-dimethylamino) anil are heated with 20 parts by weight of 4-methyl-6-chloro-3-oxythionaphthene in 500 parts by weight of glacial acetic acid at 70 ° C. for 10 hours.

   The dye, which is vacuumed off and washed neutrally after it cools, dyes cotton in very beautiful, lively, blue-tinged pink tones that are fast to light, wash and stomach.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung von 4.4'-Di- methyl-5.7.6'-trichlorthioindigo, dadurch gekennzeichnet, dass 4-Methyl-5.7-dichlor- 2 . 3-diketodihydrothionaphthenchinon- 2- (p- (limethylamino)-anil mit 4-Methyl-6-chlor-?3- oxythionaphthen kondensiert wird. Der so erhaltene Farbstoff färbt Baum wolle in sehr schönen, lebhaften, blaustichi- gen Rosa.tönen von sehr guter Licht-, Wasch- und Bäuchechtheit an. PATENT CLAIM: Process for the preparation of 4.4'-dimethyl-5.7.6'-trichlorothioindigo, characterized in that 4-methyl-5.7-dichloro-2. 3-diketodihydrothionaphthenquinone- 2- (p- (limethylamino) -anil is condensed with 4-methyl-6-chloro-? 3- oxythionaphthene. The dye thus obtained dyes cotton in very beautiful, vivid, bluish shades of pink very good light, wash and stomach fastness. UNTERANSPRUCH: Verfahren nach Patentanspruch, dadurch gekennzeichnet, dass die Kondensation durch Erhitzen in Eisessig ausgeführt wird. SUBClaim: Method according to claim, characterized in that the condensation is carried out by heating in glacial acetic acid.
CH149421D 1929-07-08 1930-06-24 Process for the preparation of a vat dye. CH149421A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE149421X 1929-07-08

Publications (1)

Publication Number Publication Date
CH149421A true CH149421A (en) 1931-09-15

Family

ID=5673333

Family Applications (1)

Application Number Title Priority Date Filing Date
CH149421D CH149421A (en) 1929-07-08 1930-06-24 Process for the preparation of a vat dye.

Country Status (1)

Country Link
CH (1) CH149421A (en)

Similar Documents

Publication Publication Date Title
CH149421A (en) Process for the preparation of a vat dye.
DE540862C (en) Process for the preparation of thioindigoid dyes
DE745417C (en) Process for the preparation of asymmetrical thioindigo dyes
DE582688C (en) Process for the preparation of o-oxyazo dyes
DE518951C (en) Process for the preparation of purple indigoid dyes
DE536294C (en) Process for the preparation of Kuepen dyes of the anthraquinone series
CH183205A (en) Process for the preparation of an azo dye.
CH175252A (en) Process for the preparation of an anthraquinone dye.
CH179677A (en) Process for the preparation of a monoazo dye.
CH179676A (en) Process for the preparation of a monoazo dye.
CH148687A (en) Process for the preparation of a vat dye.
CH197285A (en) Process for the preparation of a dye of the anthraquinone series.
CH262960A (en) Process for the preparation of a monoazo dye.
CH247598A (en) Process for the preparation of a new monoazo dye.
CH98218A (en) Process for the preparation of an o-oxymonoazo dye.
CH121345A (en) Process for the preparation of a violet vat dye of the 2-thionaphthene-2-indolindigo series.
CH187331A (en) Process for the preparation of an o-oxyazo dye.
CH101764A (en) Process for the preparation of a vat dye.
CH187337A (en) Process for the preparation of an o-oxyazo dye.
CH178549A (en) Process for the preparation of an unsymmetrical dye of the thioindigo series.
CH148688A (en) Process for the preparation of a vat dye.
CH300450A (en) Process for the preparation of an acidic monoazo dye.
CH151569A (en) Process for the preparation of a dye of the thioindigo series.
CH179678A (en) Process for the preparation of a monoazo dye.
CH134946A (en) Process for the preparation of 4,6-dimethyl-5-chloro-4'-methyl-5'.6'-dichlorothioindigo.