CH104243A - Process for the production of a vat dye of the anthraquinone series. - Google Patents
Process for the production of a vat dye of the anthraquinone series.Info
- Publication number
- CH104243A CH104243A CH104243DA CH104243A CH 104243 A CH104243 A CH 104243A CH 104243D A CH104243D A CH 104243DA CH 104243 A CH104243 A CH 104243A
- Authority
- CH
- Switzerland
- Prior art keywords
- molecule
- vat dye
- red
- anthraquinone series
- brown
- 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
- C09B5/44—Azines of the anthracene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Znsatzpaf;ent zum Hauptpatent Nr. 93280. Verfahren zur Herstellung eines Iiüpenfarbstoffes der Anthrachinonreihe. Es wurde gefunden, dass man einen neuen Küpenfarbstoff der Anthrachinonreihe her stellen kann, wenn man 1 Molekül 2 : 3-Di- aminoanthraehinon mit 1 Molekül 6-Brom- 1 :2-naphtochinon kondensiert und auf das so erhaltene Produkt 1 Molekül 1-Aminoan- thrachinon einwirken lässt.
Der so gewonnene Küpenfarbstoff bildet ein braunrotes Pulver, das sich in Nitrobenzol schwer mit roter, in konzentrierter Schwefelsäure mit brauner Farbe löst. Mit Hydrosulfit und Natronlauge wird eine braune Küpe erhalten, aus welcher Baumwolle in satten, vorzüglich echten rot braunen Tönen gefärbt wird.
<I>Beispiel:</I> 18 Teile 6-Brom-1 :2-naphtochinon und 15 Teile 2.3-Diaminoanthrachinon werden in 180 Teile Eisessig eingetragen, hierauf unter stetem Rühren langsam auf 90 bis 100 erhitzt. Man rührt weiter bei dieser Tempe ratur, bis die Reaktion stattgefunden hat, lässt dann erkalten, filtriert, wäscht den Rückstand reichlich mit heissem Wasser und trocknet. Das so erhaltene Produkt bildet ein grün gelbes Pulver, das sieh mit blauvioletter Farbe in konzentrierter Schwefelsäure löst.
9 Teile dieses Produktes werden nun zu sammen zeit 6 Teilen 1-Aminoanthra:chinon, 6 Teilen entwässertem Natriumacetat, 1ss Teil entwässertem Cuprichlorid und 300 Teilen Nitrobenzol 16 Stunden am Rückflusskühler gekocht. Naoh dem Erkalten wird abgesaugt, der Rückstand nacheinander mit Alkohol, ver dünnter Salzsäure und heissem Wasser gewa schen und getrocknet.
Znsatzpaf; ent to the main patent No. 93280. Process for the production of a liquid dye of the anthraquinone series. It has been found that a new vat dye of the anthraquinone series can be produced if 1 molecule of 2: 3-di-aminoanthraehinone is condensed with 1 molecule of 6-bromo-1: 2-naphthoquinone and 1 molecule of 1-aminoane is condensed onto the product thus obtained - lets thrachinon take effect.
The vat dye obtained in this way forms a brownish-red powder that is difficult to dissolve in nitrobenzene with red, in concentrated sulfuric acid with brown color. With hydrosulfite and caustic soda, a brown vat is obtained, from which cotton is dyed in rich, exquisitely genuine red-brown tones.
<I> Example: </I> 18 parts of 6-bromo-1: 2-naphthoquinone and 15 parts of 2,3-diaminoanthraquinone are introduced into 180 parts of glacial acetic acid, then slowly heated to 90 to 100 with constant stirring. The mixture is stirred at this temperature until the reaction has taken place, then allowed to cool, filtered, the residue is washed copiously with hot water and dried. The product obtained in this way forms a green-yellow powder, which dissolves in concentrated sulfuric acid with a blue-violet color.
9 parts of this product are now 6 parts of 1-aminoanthra: quinone, 6 parts of dehydrated sodium acetate, 1ss part of dehydrated cupric chloride and 300 parts of nitrobenzene are refluxed for 16 hours. After cooling, the residue is filtered off with suction, washed successively with alcohol, dilute hydrochloric acid and hot water and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH93280T | 1921-02-11 | ||
CH104243T | 1923-04-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH104243A true CH104243A (en) | 1924-05-16 |
Family
ID=25704645
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH104243D CH104243A (en) | 1921-02-11 | 1923-04-25 | Process for the production of a vat dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH104243A (en) |
-
1923
- 1923-04-25 CH CH104243D patent/CH104243A/en unknown
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