CH205796A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH205796A CH205796A CH205796DA CH205796A CH 205796 A CH205796 A CH 205796A CH 205796D A CH205796D A CH 205796DA CH 205796 A CH205796 A CH 205796A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- monoazo dye
- dye
- oxynaphthalene
- diazotized
- 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
- C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
- C09B29/28—Amino naphthols
- C09B29/30—Amino naphtholsulfonic acid
-
- 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
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/16—Naphthol-sulfonic acids
-
- 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 Monoazofarbstoffes. Gegenstand des vorliegenden Zusatz patentes ist ein Verfahren zur Herstellung eines Monoa.zofarbstoffes, dadurch gekenn- zeiehnet, dass man 2-Amino-1-phenoloctyl- äther diazotiert und. mit. 2-Phenylamino-8- oxynaphthalin-6-sulfons,äure kuppelt.
Der so erhaltene Farbstoff färbt Wolle und Seide aus saurem und neutralem Bade in rots:tichig braunen Tönen.
<I>Beispiel:</I> 22.,1 Teile 2-Amino-l-phenoloctyläther werden in 100 Teilen Äthylalkohol 95ö und 35 Teilen kouz. ,Salzsäure gelöst und bei<B>10'</B> mit einer konzentrierten wässrigen Lösung von 7 Teilen Natriumnitrit diazotiert. Die Diazoniumver bindung lässt man zu einer soda alkalischen Lösung von 31,5 Teilen 2-Phenyl- amino-8-oxynaphthalin-6-sulfonsä.ure fliessen.
Die Kupplung ist in kurzer Zeit beendet. Der Farbstoff wird abfiltriert, gepresst und ge trocknet. Er bildet ein dunkles Pulver, das sich in Wasser braunrot, in konz. Schwefel säure violett löst.
Process for the preparation of a monoazo dye. The subject of the present additional patent is a process for the production of a Monoa.zo dye, characterized in that 2-amino-1-phenol octyl ether is diazotized and. With. 2-Phenylamino-8-oxynaphthalene-6-sulfonic acid couples.
The dye obtained in this way dyes wool and silk from acidic and neutral baths in shades of red: tinged brown.
<I> Example: </I> 22., 1 part of 2-amino-1-phenol octyl ether is dissolved in 100 parts of ethyl alcohol 95ö and 35 parts of kouz. Dissolved hydrochloric acid and diazotized at <B> 10 '</B> with a concentrated aqueous solution of 7 parts of sodium nitrite. The diazonium compound is allowed to flow into an alkaline soda solution of 31.5 parts of 2-phenylamino-8-oxynaphthalene-6-sulfonic acid.
The coupling is completed in a short time. The dye is filtered off, pressed and dried. It forms a dark powder that turns brownish-red in water, in conc. Sulfur acid dissolves violet.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH201288T | 1937-11-13 | ||
CH205796T | 1937-11-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH205796A true CH205796A (en) | 1939-06-30 |
Family
ID=25723691
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH205796D CH205796A (en) | 1937-11-13 | 1937-11-13 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH205796A (en) |
-
1937
- 1937-11-13 CH CH205796D patent/CH205796A/en unknown
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