CH176362A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH176362A CH176362A CH176362DA CH176362A CH 176362 A CH176362 A CH 176362A CH 176362D A CH176362D A CH 176362DA CH 176362 A CH176362 A CH 176362A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- indigoid dye
- methyl
- oxynaphthalene
- 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
- C09B7/00—Indigoid dyes
- C09B7/08—Other indole-indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
Verfahren zur Herstellung eines indigolden Farbstoffes. Es wurde gefunden, dass man einen indi- goiden Farbstoff erhalten kann, wenn man die reaktionsfähigen a-Derivate des 4-Methyl- 7-chlorisatins mit 4-Methoxy-l-oxynaphthalin kondensiert.
Der Farbstoff der Formel
EMI0001.0010
stellt ein blaues Kristallpulver dar, das sich in konzentrierter Schwefelsäure mit grüner Farbe löst und beim Bedrucken der Baum wolle sehr echte blaue Töne ergibt.
Beispiel 19,8 Teile 4-Methyl-7-chlorisatir) werden durch einstündiges Erwärmen mit 22 Teilen Phosphorpentachlorid und 400 Teilen- Chlor benzol auf 95-100 in das 4-Methyl-7- chlorisatin-a-chlorid übergeführt und mit einer bei 45-50 hergestellten Lösung von 18 Teilen 4-Methoxy-l-oxynaphthalin in 500 Teilen Chlorbenzol vereinigt. Der als blaues Kristallpulver sich abscheidende Farbstoff wird filtriert, mit Chlorbenzol, sowie mit Alkohol gewaschen und getrocknet.
Zu demselben Farbstoff gelangt man, wenn statt in chlorbenzolischer Lösung in wässerigem Medium gearbeitet wird, oder wenn an Stelle des 4-Methyl-7-chlorisatin- a-chlorids das 4-Methyl-7-chlorisatin-a-anilid mit 4-Methoxy-l-oxynaphthalin in Essigsäure anhydrid erhitzt wird.
Process for the production of an indigolden dye. It has been found that an indigoid dye can be obtained if the reactive α-derivatives of 4-methyl-7-chloroisatin are condensed with 4-methoxy-1-oxynaphthalene.
The dye of the formula
EMI0001.0010
represents a blue crystal powder that dissolves in concentrated sulfuric acid with a green color and produces very real blue tones when the cotton is printed.
EXAMPLE 19.8 parts of 4-methyl-7-chlorisatin) are converted into 4-methyl-7-chlorisatin-a-chloride by heating for one hour with 22 parts of phosphorus pentachloride and 400 parts of chlorobenzene to 95-100 and with a at 45 -50 prepared solution of 18 parts of 4-methoxy-1-oxynaphthalene combined in 500 parts of chlorobenzene. The dye which separates out as blue crystal powder is filtered, washed with chlorobenzene and with alcohol and dried.
The same dye is obtained when working in an aqueous medium instead of in a chlorobenzene solution, or when 4-methyl-7-chloroisatin-a-anilide with 4-methoxy- l-oxynaphthalene is heated in acetic anhydride.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH176362T | 1934-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH176362A true CH176362A (en) | 1935-04-15 |
Family
ID=4426916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH176362D CH176362A (en) | 1934-04-20 | 1934-04-20 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH176362A (en) |
-
1934
- 1934-04-20 CH CH176362D patent/CH176362A/en unknown
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