CH233574A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH233574A CH233574A CH233574DA CH233574A CH 233574 A CH233574 A CH 233574A CH 233574D A CH233574D A CH 233574DA CH 233574 A CH233574 A CH 233574A
- Authority
- CH
- Switzerland
- Prior art keywords
- parts
- dye
- production
- vat
- vat dye
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/34—Anthraquinone acridones or thioxanthrones
- C09B5/40—Condensation products of benzanthronyl-amino-anthraquinones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Cosmetics (AREA)
Description
Verfahren zur Herstellung eines Küpenfarbstoffes. Es wurde gefunden, dass man einen wert vollen Küpenfarbstoff erhält, wenn man den durch Umsetzen von 6,Bz1-Dibrombenz- anthron zunächst mit 1 Mol 1-Aminoanthra- cUinon und dann mit 1 Mol 1-Amino-2-cyan- anthrachinon erhältlichen Stoff mit alka lischen Kondensationsmitteln behandelt.
Der neue Farbstoff färbt Baumwolle aus ,der Küpe in braunstichig oliven, gut egali sierten, chlor- und sodakochechten Tönen.
Die in folgendem Beispiel genannten Teile sind Gewichtsteile.
<I>Beispiel:</I> Ein Gemisch aus 50 Teilen 6,Bzl-Di- bro-mbenzanthron, 28,<B>8</B> Teilen 1 - Amino- anthrachinon, 19,3 Teilen wasserfreiem Na- triumcarbonat, 1,9 Teilen fein verteiltem Kupferoxyd und 480 Teilen Nitrobenzol wird unter Rühren mehrere Stunden zum Sieden erhitzt.
Dann lässt man auf 170-180 ' ab kühlen, trägt 32,1 Teile 1-Amino-2-cyan- anthrachinon, <B>1.9,3</B> Teile wasserfreies Na- triumcarbonat und 1,9 Teile Kupferoxyd ein und erhitzt hierauf das Ganze etwa 15 Stun den zum Sieden.
Nach dem Abkühlen auf 80 bis 90 saugt man das ausgeschiedene Imid ab, befreit es in üblicher Weise von anhaften dem Lösungsmittel und anorganischen Bei- mengungen und trocknet es.
100 Teile dieses Imids trägt man unter Rühren in,eine etwa 100-105 heisse Schmelze von 400 Teilen Kaliumhydroxyd und 400 Tei len Äthanof@ein und rührt date Gemisch 5 Stun den bei dieser Temperatur weiter. Dann giesst man in Wasser kocht unter Einleiten von Luft bis der Farbstoff sich ausgeschieden hat, saugt ihn ab, wäscht mit Wasser aus und trocknet.
Man erhält so -einen Farbstoff, ,der Baum wolle aus der alkalischen Hydrosulfitküpe in braunstichig oliven Tönen färbt. Das Egali- eiervermögen, die Chlor- und So:dakochecht- heit des neuen Farbstoffes ist besser als .die des entsprechenden Farbstoffes aus 6,Bzl- Di-(1''-anthra@chinonyl)-amino-benzanthron.
Process for the production of a vat dye. It has been found that a valuable vat dye is obtained if the substance obtainable by reacting 6, Bz1-dibromobenzanthrone first with 1 mole of 1-aminoanthracuinone and then with 1 mole of 1-amino-2-cyanoanthraquinone treated with alkaline condensation agents.
The new dye dyes cotton, the vat in brownish olive, well-leveled, chlorine- and soda-proof shades.
The parts mentioned in the following example are parts by weight.
<I> Example: </I> A mixture of 50 parts of 6, Bzl-dibro-mbenzanthron, 28, <B> 8 </B> parts of 1 - amino anthraquinone, 19.3 parts of anhydrous sodium carbonate, 1.9 parts of finely divided copper oxide and 480 parts of nitrobenzene are heated to boiling for several hours while stirring.
The mixture is then allowed to cool to 170-180 ', 32.1 parts of 1-amino-2-cyano-anthraquinone, 1.9.3 parts of anhydrous sodium carbonate and 1.9 parts of copper oxide are introduced and the mixture is heated then boil for about 15 hours.
After cooling to 80 to 90, the precipitated imide is filtered off with suction, freed from adhering solvent and inorganic additions in the usual way and dried.
100 parts of this imide are introduced into an approximately 100-105 hot melt of 400 parts of potassium hydroxide and 400 parts of ethane, with stirring, and the mixture is stirred for 5 hours at this temperature. Then it is poured into water and boiled while air is passed in until the dye has separated out, sucks it off, washed out with water and dried.
This gives a dye, the cotton dyes from the alkaline hydrosulfite vat in brownish olive tones. The leveling capacity, the chlorine and So: dakochfastness of the new dye is better than that of the corresponding dye from 6, Bzl-di- (1 "- anthra @ quinonyl) -amino-benzanthrone.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE233574X | 1941-02-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH233574A true CH233574A (en) | 1944-08-15 |
Family
ID=5886847
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH233574D CH233574A (en) | 1941-02-21 | 1943-04-22 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH233574A (en) |
-
1943
- 1943-04-22 CH CH233574D patent/CH233574A/en unknown
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