CH234528A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH234528A CH234528A CH234528DA CH234528A CH 234528 A CH234528 A CH 234528A CH 234528D A CH234528D A CH 234528DA CH 234528 A CH234528 A CH 234528A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- vat dye
- vat
- benzacridone
- 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
- C09B5/002—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being condensed in peri position and in 1-2 or 2-3 position
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 232371. Verfahren zur Herstellung eines Nüpenfarbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines neuen Kü- penfarbstoffes durch Umsetzung von 4-Amino- 3'. 5'- dichloranthrachinon - 2.1- (N) -1'.
2'- (N)- benzacridon mit dem Halogenid der nachste henden Formel
EMI0001.0011
Die Umsetzung wird vorteilhaft in Gegen wart eines indifferenten Lösungsmittels, wie Nitrobenzol, Trichlorbenzol oder Phenol, bei erhöhten Temperaturen durchgeführt.
Der erhältliche Farbstoff färbt Baum wolle aus weinroter güpe in sehr gelbstichig grünen Tönen von sehr guten Echtheiten an.
Das als Ausgangsmaterial benutzte Ha- logenid der obenstehenden Formel kann im Falle des Chlorids aus dem bekannten 8 Brom-2-phenol-4-ogy-6.7 - phthaloylchinazolin durch Umsatz mit Hydrazinhydrat zum ent sprechenden Pyrazolanthronderivat, Benzoy- lieren der NH-Gruppe und nachfolgende Be handlung mit Phosphorpentachlorid in einem indifferenten organischenLösungsmittel, zum Beispiel Nitrobenzol oder Trichlorbenzol,
her gestellt werden. Es muss dahingestellt blei ben, ob die Benzoylgruppe bei einer der nachfolgenden Operationen abgespalten wird oder nicht.
<I>Beispiel:</I> 29 Gewichtsteile des Chlorids der Formel
EMI0001.0033
und 15 Gewichtsteile 4-Amino-3'.5'-dichlor- anthrachinon-'2.1- (N) -1'. 2'- (N) -benzacridon werden in 350 Gewichtsteilen Phenol bis zur Beendigung der Salzsäureentwicklung zum Sieden erhitzt. Dann wird die Schmelze bei 130 mit warmem Nitrobenzol verdünnt und bei 90 abgesaugt. Der Farbstoff (olivgrüne Nädelchen) wird durch Auskochen mit Pyri- din gereinigt und durch Verpasten aus kon zentrierter Schwefelsäure auf die übliche Weise in einen Färbeteig übergeführt.
Er färbt Baumwolle aus weinroter Küpe in sehr gelbstichig grünen Tönen von sehr guten Echtheiten.
<B> Additional patent </B> to main patent no. 232371. Process for the production of a pebble dye. The present patent relates to a process for the production of a new vat dye by reacting 4-amino-3 '. 5'-dichloroanthraquinone - 2.1- (N) -1 '.
2'- (N) - benzacridone with the halide of the following formula
EMI0001.0011
The reaction is advantageously carried out in the presence of an inert solvent, such as nitrobenzene, trichlorobenzene or phenol, at elevated temperatures.
The available dye dyes cotton from wine-red güpe in very yellowish green shades of very good fastness properties.
The halide of the above formula used as starting material can, in the case of the chloride, from the known 8 bromo-2-phenol-4-ogy-6.7-phthaloylquinazoline by reaction with hydrazine hydrate to form the corresponding pyrazolanthrone derivative, benzoylate the NH group and the following Treatment with phosphorus pentachloride in an inert organic solvent, for example nitrobenzene or trichlorobenzene,
getting produced. It remains to be seen whether the benzoyl group is split off in one of the subsequent operations or not.
<I> Example: </I> 29 parts by weight of the chloride of the formula
EMI0001.0033
and 15 parts by weight of 4-amino-3'.5'-dichloro-anthraquinone-'2.1- (N) -1 '. 2'- (N) -benzacridone are heated to boiling in 350 parts by weight of phenol until the evolution of hydrochloric acid has ended. Then the melt is diluted at 130 with warm nitrobenzene and sucked off at 90. The dye (olive-green needles) is cleaned by boiling with pyridine and converted into a dyed paste in the usual way by pasting concentrated sulfuric acid.
It dyes cotton from a wine-red vat in very yellowish green tones with very good fastness properties.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE234528X | 1939-05-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH234528A true CH234528A (en) | 1944-09-30 |
Family
ID=5892000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH234528D CH234528A (en) | 1939-05-26 | 1941-06-20 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH234528A (en) |
-
1941
- 1941-06-20 CH CH234528D patent/CH234528A/en unknown
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