CH137116A - Process for the preparation of a nitrogenous vat dye of the benzanthrone series. - Google Patents
Process for the preparation of a nitrogenous vat dye of the benzanthrone series.Info
- Publication number
- CH137116A CH137116A CH137116DA CH137116A CH 137116 A CH137116 A CH 137116A CH 137116D A CH137116D A CH 137116DA CH 137116 A CH137116 A CH 137116A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- blue
- nitrogenous
- vat dye
- 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/22—Dibenzanthrones; Isodibenzanthrones
- C09B3/24—Preparation by synthesis of the nucleus
- C09B3/26—Preparation by synthesis of the nucleus from dibenzanthronyls
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines stickstoffhaltigen Küpenfarbstoffes der Benzanthronreihe. In dem Hauptpatent Nr. 120525 ist ein Verfahren zur Darstellung eines Küpenfarb- stoffes beschrieben, bei dem a-Anthrachinonyl- amino Bz1. Bzl'-benzantbronylsulfid mit ei nem alkalischen Kondensationsmittel, insbe sondere alkoholischem Alkali, behandelt wird.
Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung eines stickstoff haltigen Küpenfarbstoffes der Benzanthron- reihe, bei dem das Kondensationsprodukt aus 6-Halogen-Bzl-parathiokresylbenzanthron und 1-Aminoanthrachinon mit alkalischen Mitteln, insbesondere alkoholischem Alkali, behandelt wird.
Der neue Farbstoff färbt aus blauer Küpe die pflanzliche Faser in echten, blau stichigschwarzen Tönen und löst sich in konzentrierter Schwefelsäure mit trüb blau stichig grüner Farbe. Beispiele 1. 10 Teile des Kondensationsproduktes aus 6-Halogen-Bzl-thiokresylbenzanthron (er hältlich zum Beispiel durch Erhitzen von 6 Halogen-Bzl-brombenzanthron mit der berech neten Menge p-Thiokresol und Kalihydroxyd in alkoholischer Lösung) und 1-Aminoanthra- chinon werden mit 40 Teilen Kalium hydroxyd und 25-30 Teilen Alkohol so lange bei 170-180 verschmolzen,
bis die Farbstoffbildung beendet ist. Die Schmelze wird in der üblichen Weise aufgearbeitet.
2. 10 Teile des Kondensationsproduktes aus 6-Halogen-Bzl-parathiokresylbenzanthron und 1-Aminoanthrachinon werden bei unge fähr 240-250 in die acht- bis zehnfache Menge geschmolzenes Kaliumhydroxyd ein getragen. Man erhöht die Temperatur der Schmelze auf etwa 260-270 und rührt so lange, bis die Farbstoffbildung beendet ist. Die erkaltete Schmelze wird in Wasser aufgenommen, kochend filtriert und gewa schen.
Process for the preparation of a nitrogenous vat dye of the benzanthrone series. The main patent no. 120525 describes a process for the preparation of a vat dye in which a-anthraquinonylamino Bz1. Bzl'-benzantbronyl sulfide is treated with an alkaline condensing agent, in particular special alcoholic alkali.
The subject of this additional patent is a process for the preparation of a nitrogen-containing vat dye of the benzanthrone series, in which the condensation product of 6-halo-Bzl-parathiocresylbenzanthrone and 1-aminoanthraquinone is treated with alkaline agents, especially alcoholic alkali.
The new dye dyes the vegetable fibers from a blue vat in real, blue, pungent black tones and dissolves in concentrated sulfuric acid with a cloudy blue, pungent green color. Examples 1. 10 parts of the condensation product of 6-halo-Bzl-thiocresylbenzanthrone (it can be obtained, for example, by heating 6 halo-Bzl-bromobenzanthrone with the calculated amount of p-thiocresol and potassium hydroxide in alcoholic solution) and 1-aminoanthraquinone fused with 40 parts of potassium hydroxide and 25-30 parts of alcohol at 170-180,
until dye formation is complete. The melt is worked up in the usual way.
2. 10 parts of the condensation product of 6-halo-Bzl-parathiocresylbenzanthrone and 1-aminoanthraquinone are carried at around 240-250 in eight to ten times the amount of molten potassium hydroxide. The temperature of the melt is increased to about 260-270 and the mixture is stirred until the formation of the dye has ended. The cooled melt is taken up in water, filtered at the boil and washed.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH137116T | 1928-06-14 | ||
CH120525T | 1929-08-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH137116A true CH137116A (en) | 1929-12-15 |
Family
ID=25709472
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH137116D CH137116A (en) | 1928-06-14 | 1928-06-14 | Process for the preparation of a nitrogenous vat dye of the benzanthrone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH137116A (en) |
-
1928
- 1928-06-14 CH CH137116D patent/CH137116A/en unknown
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