CH263847A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH263847A CH263847A CH263847DA CH263847A CH 263847 A CH263847 A CH 263847A CH 263847D A CH263847D A CH 263847DA CH 263847 A CH263847 A CH 263847A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- vat
- dye
- vat dye
- parts
- 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
- C09B5/26—Carbazoles of the anthracene series
- C09B5/28—Anthrimide carbazoles
-
- 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
- C09B5/26—Carbazoles of the anthracene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 257722. Verfahren zur Herstellung eines Küpenfarbstoffes. Es wurde gefunden, dass ein wertvoller Küpenfarbstoff hergestellt werden kann, wenn man das Kondensationsprodukt aus 1 Mol 3',6'-Diehlor-3,4-phthaloyl-pyren und 2 Mol 1-Aminoanthrachinon der Formel
EMI0001.0007
mit carbazolierenden Mitteln behandelt.
Der neue Farbstoff ist ein dunkles Pulver, das sich in konzentrierter Schwefelsäure mit rötlichbrauner Farbe löst und Baumwolle aus rotbrauner Küpe in sehwärzlichen Braun tönen färbt.
<I>Beispiel:</I> 60 Teile Aluminiumchlorid werden in 130 Teile trockenes Pyridin eingetragen und 10 Teile Pyridin abdestillieren gelassen. Bei einer Temperatur von 121-123 werden 6 Teile des Kondensationsproduktes aus 1 Mol 3',6'-Dichlor-3,4-phthaloyl-pyren und 2 Mol 1-Aminoanthrachinon zugefügt und 1 Stunde bei dieser Temperatur gerührt.
Die Schmelze wird in Wasser ausgetragen, mit Natronlauge alkalisch gestellt, mit. Natriumhydrosulfit ver- küpt und von wenig Verunreinigungen abfil- triert. Nach dem Ausblasen mit Luft, Abfil- trieren, Auswaschen und Trocknen stellt der Farbstoff ein dunkles Pulver dar. Durch Naehoxydieren in schwefelsaurer Lösung mit Dichromat bei erhöhter Temperatur. kann der Farbstoff noch etwas gereinigt werden.
Zu einem gleichfärbenden Farbstoff ge langt man auch, wenn die Carbazolierung bei einer Temperatur von 140 durchgeführt wird, oder wenn man nur 30 Teile Alumi niumchlorid und etwa 70 Teile Pyridin ver wendet.
<B> Additional patent </B> to main patent No. 257722. Process for the production of a vat dye. It has been found that a valuable vat dye can be produced if the condensation product of 1 mole of 3 ', 6'-Diehlor-3,4-phthaloyl-pyrene and 2 moles of 1-aminoanthraquinone of the formula
EMI0001.0007
treated with carbazolating agents.
The new dye is a dark powder that dissolves in concentrated sulfuric acid with a reddish-brown color and dyes cotton from a reddish-brown vat in blackish brown tones.
<I> Example: </I> 60 parts of aluminum chloride are introduced into 130 parts of dry pyridine and 10 parts of pyridine are allowed to distill off. At a temperature of 121-123 6 parts of the condensation product of 1 mole of 3 ', 6'-dichloro-3,4-phthaloyl-pyrene and 2 moles of 1-aminoanthraquinone are added and the mixture is stirred at this temperature for 1 hour.
The melt is discharged into water, made alkaline with sodium hydroxide solution, with. Sodium hydrosulphite is vat and a few impurities are filtered off. After blowing out with air, filtering off, washing out and drying, the dyestuff is a dark powder. By oxidizing in sulfuric acid solution with dichromate at elevated temperature. the dye can still be cleaned a little.
A dye of the same color is also obtained if the carbazolation is carried out at a temperature of 140, or if only 30 parts of aluminum chloride and about 70 parts of pyridine are used.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH257722T | 1946-03-29 | ||
CH263847T | 1946-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH263847A true CH263847A (en) | 1949-09-15 |
Family
ID=25730114
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH263847D CH263847A (en) | 1946-03-29 | 1946-03-29 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH263847A (en) |
-
1946
- 1946-03-29 CH CH263847D patent/CH263847A/en unknown
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