CH123457A - Process for the preparation of a vat dye from 4-methyl-5. 6-dichloro-3-oxy-1-thionaphtene. - Google Patents
Process for the preparation of a vat dye from 4-methyl-5. 6-dichloro-3-oxy-1-thionaphtene.Info
- Publication number
- CH123457A CH123457A CH123457DA CH123457A CH 123457 A CH123457 A CH 123457A CH 123457D A CH123457D A CH 123457DA CH 123457 A CH123457 A CH 123457A
- Authority
- CH
- Switzerland
- Prior art keywords
- oxy
- dichloro
- methyl
- preparation
- thionaphtene
- Prior art date
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- Coloring (AREA)
Description
Verfahren zur Darstellung eines IZüpenfarbstoffes aus 4-Nethyl-ö. 6-diehlor-3-oay- 1-thionaphten. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung eines Farbstoffes, durch Kondensation eines reaktionsfähigen 2-Derivates des 4-Methyl-5 . 6-dichlor-3-oxy- 1-thionaphtens mit 4-Brom-3 . 2-(3'-oxy-1'- i;hiophen)-naphtalin.
EMI0001.0013
<I>Beispiel:
</I> 24 Gewichtsteile 4-Methyl-5 . 6-dichlor-3- oxythionaphten werden in Sprit und Alkali gelöst und mit einer alkoholischen Lösung von 25 Gewichtsteilen 4-Nitroso-dimethyl- anilin versetzt. Das 4-Methyl-5 . 6-dichlor- 2 . 3-dihydro-3-ketothionaphten- 2 - (4' -dime- thylamino)-anil scheidet sich nach kurzem Rühren vollständig ab.
Es wird abgesaugt und mit 28 Gewichtsteilen 4-Brom-3. 2-(3'- oxy-1'-thiophen)-naphtalin und 400 Ge wichtsteilen Eisessig mehrere Stunden ge- kocht. Nach dem Erkalten saugt man ab und wäscht neutral.
Der Farbstoff löst sich in Nitrobenzol mit blaustichig roter Farbe und violetter Fluoreszenz, gibt eine gelbrote Küpe und färbt Baumwolle in violetten Tönen von be sonders guten Echtheitseigenschaften.
Process for the preparation of an IZüpen dye from 4-Nethyl-ö. 6-diehlor-3-oay-1-thionaphten. The subject of this additional patent is a process for the preparation of a dye by condensation of a reactive 2-derivative of 4-methyl-5. 6-dichloro-3-oxy-1-thionaphthene with 4-bromo-3. 2- (3'-oxy-1'- i; hiophene) naphthalene.
EMI0001.0013
<I> example:
</I> 24 parts by weight of 4-methyl-5. 6-dichloro-3-oxythionaphthene are dissolved in fuel and alkali and mixed with an alcoholic solution of 25 parts by weight of 4-nitroso-dimethylaniline. The 4-methyl-5. 6-dichloro-2. 3-dihydro-3-ketothionaphten- 2 - (4 '-dimethylamino) -anil separates out completely after brief stirring.
It is filtered off and with 28 parts by weight of 4-bromo-3. 2- (3'-oxy-1'-thiophene) naphthalene and 400 parts by weight of glacial acetic acid boiled for several hours. After cooling, it is suctioned off and washed neutral.
The dye dissolves in nitrobenzene with a bluish red color and violet fluorescence, gives a yellow-red vat and dyes cotton in violet shades with particularly good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE123457X | 1925-05-06 | ||
CH120807T | 1926-05-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH123457A true CH123457A (en) | 1927-11-16 |
Family
ID=25709578
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH123457D CH123457A (en) | 1925-05-06 | 1926-05-03 | Process for the preparation of a vat dye from 4-methyl-5. 6-dichloro-3-oxy-1-thionaphtene. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH123457A (en) |
-
1926
- 1926-05-03 CH CH123457D patent/CH123457A/en unknown
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