CH188539A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH188539A CH188539A CH188539DA CH188539A CH 188539 A CH188539 A CH 188539A CH 188539D A CH188539D A CH 188539DA CH 188539 A CH188539 A CH 188539A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- production
- bromo
- chloro
- indigoid 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
- C09B7/00—Indigoid dyes
- C09B7/08—Other indole-indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent zum</B> Hauptpatent Nr. 186851. Verfahren zur Herstellung eines indigolden Farbstoffes. Es wurde gefunden, dass man einen indi- goiden Farbstoff herstellen kann, wenn man die reaktionsfähigen a-Derivate des 4-Chlor- 5-brom-7-methoxyisatins mit 1-Oxyanthracen kondensiert.
Der Farbstoff der Formel
EMI0001.0011
stellt ein schwach grünstichig blaues Pulver dar, das sich in konzentrierter Schwefelsäure mit grüner Farbe löst und beim Bedrucken der Baumwolle grünstichig blaue Farbtöne liefert, die sich durch sehr gute Wasch- und Chlorechtheit auszeichnen.
<I>Beispiel:</I> 29 Teile 4-Chlor-5-brom-7-methoxyisatin werden durch Erwärmen mit 22 Teilen Phos- phorpentachlorid in 350 Teilen Chlorbenzol in das 4-Chlor-5-brom-7-methoxyisatin-a-chlorid übergeführt und mit einer bei 45-600 her gestellten Lösung von 19,4 Teilen 1-Oxy- anthracen in 500 Teilen Chlorbenzol vereinigt. Der Farbstoff wird filtriert, mit Chlorbenzol sowie mit Alkohol gewaschen und getrocknet.
Zu demselben Farbstoff gelangt man, wenn statt in chlorbenzolischer Lösung in wässeri gem Medium gearbeitet wird, oder wenn an Stelle des 4-Chlor-5-brom-7-methogyisatin-a Chlorids das 4-Chlor-5-brom-7-methoxyisatin- a-anilid mit 1-Oxyanthracen in Essigsäure anhydrid erhitzt wird.
<B> Additional patent to </B> main patent no. 186851. Process for the production of an indigolden dye. It has been found that an indigoid dye can be produced if the reactive α-derivatives of 4-chloro-5-bromo-7-methoxyisatin are condensed with 1-oxyanthracene.
The dye of the formula
EMI0001.0011
is a slightly greenish blue powder that dissolves in concentrated sulfuric acid with a green color and, when printed on the cotton, produces greenish blue shades that are characterized by very good fastness to washing and chlorine.
<I> Example: </I> 29 parts of 4-chloro-5-bromo-7-methoxyisatin are converted into 4-chloro-5-bromo-7-methoxyisatin-a by heating with 22 parts of phosphorus pentachloride in 350 parts of chlorobenzene -Converted chloride and combined with a solution of 19.4 parts of 1-oxy-anthracene in 500 parts of chlorobenzene made at 45-600. The dye is filtered, washed with chlorobenzene and with alcohol and dried.
The same dye is obtained if instead of working in a chlorobenzene solution in an aqueous medium, or if the 4-chloro-5-bromo-7-methoxyisatin instead of the 4-chloro-5-bromo-7-methogyisatin-a chloride a-anilide is heated anhydride with 1-oxyanthracene in acetic acid.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH188539T | 1935-10-14 | ||
CH186851T | 1936-02-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH188539A true CH188539A (en) | 1936-12-31 |
Family
ID=25721454
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH188539D CH188539A (en) | 1935-10-14 | 1935-10-14 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH188539A (en) |
-
1935
- 1935-10-14 CH CH188539D patent/CH188539A/en unknown
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