CH178119A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH178119A CH178119A CH178119DA CH178119A CH 178119 A CH178119 A CH 178119A CH 178119D A CH178119D A CH 178119DA CH 178119 A CH178119 A CH 178119A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- methyl
- indigoid dye
- indigoid
- 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
- C09B7/06—Indone-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigolden Farbstoffes. Es wurde befunden, dass man einen indi- goiden Farbstoff erhalten kann, wenn man die reaktionsfähigen a-Derivate des. 4-Methyl- 5.7-dichloriea-tins mit 4-Methyl-6--chlor-3- oxythionaphthen kondensiert.
Der Farbstoff der Formel
EMI0001.0011
stellt ein rotviolettes Kristallpulver dar, das sich in konzentrierter Schwefelsäure mit grüner Farbe löst und beim Bedrucken der Baumwolle sehr echte, hervorragend reine violette Töne ergibt.
<I>Beispiel:</I> 23,1 Teile 4 - Methyl - 5 . 7 - dichlorisatin werden durch Erwärmen mit 22 Teilen Pho s- phorpentachlorid in 300 Teilen Chlorbenzol in das 4-Methyl-5 .
7--dichlorisatin-a-chlorid, ver wandelt und mit einer bei 6'0 bis<B>70'</B> herge stellten Lösung von 19,9 Teilen 4-Methyl-6- chlor-3-oxythionaphthen in 300 Teilen Chlor- benzol vereinigt. Der ale rotviolettes IC-ri- stallpulvar erhaltene Farbstoff wird filtriert. mit Chlorbenzol, sowie mit Alkohol gewa schen und getrocknet.
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-5,7-dichloroea-tin are condensed with 4-methyl-6-chloro-3-oxythionaphthene.
The dye of the formula
EMI0001.0011
is a red-violet crystal powder that dissolves in concentrated sulfuric acid with a green color and produces very real, exceptionally pure violet tones when printed on the cotton.
<I> Example: </I> 23.1 parts 4 - methyl - 5. 7-dichloroisatin are converted into 4-methyl-5 by heating with 22 parts of phosphorus pentachloride in 300 parts of chlorobenzene.
7 - dichloroisatin-a-chloride, transformed and with a solution of 19.9 parts of 4-methyl-6-chloro-3-oxythionaphthene in 300 parts prepared at 6'0 to <B> 70 '</B> Chlorobenzene combined. The dye obtained from all red-violet IC crystal powder is filtered. Washed with chlorobenzene and alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH176362T | 1934-04-20 | ||
CH178119T | 1934-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH178119A true CH178119A (en) | 1935-06-30 |
Family
ID=25719843
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH178119D CH178119A (en) | 1934-04-20 | 1934-04-20 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH178119A (en) |
-
1934
- 1934-04-20 CH CH178119D patent/CH178119A/en unknown
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