CH240127A - Process for the preparation of a new monoazo dye. - Google Patents
Process for the preparation of a new monoazo dye.Info
- Publication number
- CH240127A CH240127A CH240127DA CH240127A CH 240127 A CH240127 A CH 240127A CH 240127D A CH240127D A CH 240127DA CH 240127 A CH240127 A CH 240127A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- dye
- parts
- preparation
- red
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
- C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
- C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
- C09B29/3647—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms
- C09B29/3652—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles
- C09B29/366—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles containing hydroxy-1,2-diazoles, e.g. pyrazolone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Nonoazofarbstoifes. Gegenstand vorliegender Erfindung ist ein Verfahren zur Herstellung eines neuen sauren 1VIonoazofarbstoffes, welcher sich zum Färben tierischer Fasern eignet.
Erfindungsgemäss wird der neue Farbstoff dadurch erhalten, dass man 3-N-Äthyl-N-ss- chlorpropionylamino-4-methylanilin dianotiert und die erhaltene Diazoniumverbindung mit 2- Acetylamino-8-naphthol-6-sulfonsäure kuppelt.
Der neue Farbstoff stellt ein rotes Pulver dar, das sich in warmem Wasser und in konzentrierter Schwefelsäure unter Bildung einer gelblichroten Färbung löst.
Der neue Farbstoff färbt Wolle aus einem Schwefelsäure und Glaubersalz enthaltenden Färbebad in roten Farbtönen, die sich durch sehr gute Echtheitseigenschaften gegen starkes Waschen, Wallen und Lichtechtheit aus zeichnen.
Die Erfindung möge an Hand des nach stehenden Beispiels erläutert sein. Die Teile bedeuten Gewichtsteile. <I>Beispiel:</I> 24 Teile 3-N-Äthyl-N=ss-chlorpropionyl- amino-4-methylanilin werden in 350 Teilen Wasser und 25 Teilen 36 o/oiger Salzsäure gelöst. Hierauf werden 6,9 Teile Natriumnitrit zugesetzt. Die erhaltene Diazoniumlösung wird nun unter Rühren einem Gemisch von 30,3 Tei len Natrium-2-acetylamino-8-naphthol-6-sul- fonat, 350 Teilen Wasser und 28 Teilen krist. Natriumacetat zugegeben.
Sobald die Kupplung beendet ist, fügt man 50 Teile Natriumchlorid hinzu und filtriert alsdann den ausgeschiedenen Farbstoff ab, welcher schliess lich mit 5 o/oiger wässriger Natriumchlorid- lösung gewaschen und getrocknet wird.
Process for the preparation of a new nonoazo dye. The present invention relates to a process for the production of a new acidic 1Vionoazo dye which is suitable for dyeing animal fibers.
According to the invention, the new dye is obtained by dianotating 3-N-ethyl-N-ß-chloropropionylamino-4-methylaniline and coupling the diazonium compound obtained with 2-acetylamino-8-naphthol-6-sulfonic acid.
The new dye is a red powder that dissolves in warm water and concentrated sulfuric acid to form a yellowish-red color.
The new dye dyes wool from a dyebath containing sulfuric acid and Glauber's salt in red shades, which are characterized by very good fastness properties against heavy washing, bulging and lightfastness.
The invention may be explained using the example below. The parts mean parts by weight. <I> Example: </I> 24 parts of 3-N-ethyl-N = ß-chloropropionylamino-4-methylaniline are dissolved in 350 parts of water and 25 parts of 36% hydrochloric acid. 6.9 parts of sodium nitrite are then added. The resulting diazonium solution is then stirred into a mixture of 30.3 parts of sodium 2-acetylamino-8-naphthol-6-sulphonate, 350 parts of water and 28 parts of crystalline. Sodium acetate added.
As soon as the coupling has ended, 50 parts of sodium chloride are added and the dyestuff which has separated out is then filtered off, which is finally washed with 5% aqueous sodium chloride solution and dried.
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB240127X | 1941-12-22 | ||
GB241241X | 1941-12-24 | ||
CH237396T | 1942-12-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH240127A true CH240127A (en) | 1945-11-30 |
Family
ID=27177979
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH240127D CH240127A (en) | 1941-12-22 | 1942-12-21 | Process for the preparation of a new monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH240127A (en) |
-
1942
- 1942-12-21 CH CH240127D patent/CH240127A/en unknown
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