CH130083A - Process for the preparation of a violet vat dye of the 2-thionaphthene-2-indolindigo series. - Google Patents
Process for the preparation of a violet vat dye of the 2-thionaphthene-2-indolindigo series.Info
- Publication number
- CH130083A CH130083A CH130083DA CH130083A CH 130083 A CH130083 A CH 130083A CH 130083D A CH130083D A CH 130083DA CH 130083 A CH130083 A CH 130083A
- Authority
- CH
- Switzerland
- Prior art keywords
- series
- thionaphthene
- indolindigo
- preparation
- violet
- Prior art date
Links
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- Coloring (AREA)
Description
Verfahren zur Herstellung eines violetten Küpenfarbstoffes der 2-Thionaphten-2-indolindigoreihe. Es wurde gefunden, dass man einen neuen violetten Küpenfarbstoff erhält, wenn man 4. 7-Dimethyl-5- chloroxythionaphten mit einem 5.7-Dibromisatin kondensiert, in dessen a Stellung sich eine labile Gruppe befindet.
Der neue Farbstoff bildet ein violettblarres Pulver, das sich in konzentrierter Schwefel säure mit blaugrüner Farbe löst. Er färbt Baumwolle aus gelber Hydrosulfitküpe in violetten Tönen an. Gegenüber den bisher bekannt gewordenen Farbstoffen der 2-Thio- naphten-2-indolindigor-eihe zeichnet sich der neue Farbstoff aus durch Reinheit der Nuance und bessere Sodakochechtheit.
Das bisher noch nicht beschriebene 4.7 Dicnethyl-5-chloroxythionaphten kann man aus dem 1-Amido-4-chlor-2.5-xylol durch Über führung in die 4-Chlor-2.5-xylol-l-thioglykol- säure und deren Ringschluss nach bekannten Methoden erhalten. <I>Beispiel:</I> 30,5 Gewichtsteile 5.7-Dibromisatin wer den in etwa 300 Gewichtsteilen Chlorbenzol durch Erwärmen mit 22 Gewichtsteilen Phos- phorpentachlorid in das 5.7-Dibromisatin-a- chlorid übergeführt.
Diese Lösung wird mit einer Suspension von 21,2 Gewichtsteilen 4.7 Dimethyl-5-chloroxythionaphten in 200 Ge wichtsteilen Chlorbenzol vereinigt und einige Zeit auf<B>60-70'</B> erwärmt. Der hierbei ent standene Farbstoff wird filtriert und mit Chlorbenzol, zuletzt mit Sprit gewaschen.
In gleicher Weise kann man das 5.7 Dibromisatin-a-anilid zur Kondensation ver wenden.
Process for the preparation of a violet vat dye of the 2-thionaphthene-2-indolindigo series. It has been found that a new violet vat dye is obtained if 4. 7-dimethyl-5-chloroxythionaphthene is condensed with a 5.7-dibromoisatin in whose a position there is a labile group.
The new dye forms a violet-blue powder that dissolves in concentrated sulfuric acid with a blue-green color. He dyes cotton from a yellow hydrosulfite vat in purple tones. Compared to the previously known dyes of the 2-thionaphthene-2-indolindigor series, the new dye is distinguished by its purity of shade and better fastness to soda cooking.
The previously not yet described 4.7 diethyl-5-chloroxythionaphthene can be converted from 1-amido-4-chloro-2.5-xylene into 4-chloro-2.5-xylene-1-thioglycolic acid and ring closure by known methods receive. <I> Example: </I> 30.5 parts by weight of 5.7-dibromoisatin are converted into the 5.7-dibromoisatin a-chloride in about 300 parts by weight of chlorobenzene by heating with 22 parts by weight of phosphorus pentachloride.
This solution is combined with a suspension of 21.2 parts by weight of 4.7 dimethyl-5-chloroxythionaphthene in 200 parts by weight of chlorobenzene and heated to <B> 60-70 '</B> for some time. The resulting dye is filtered and washed with chlorobenzene and finally with fuel.
In the same way, one can use 5.7 dibromoisatin-a-anilide for condensation.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE130083X | 1926-02-19 | ||
CH127268T | 1927-02-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH130083A true CH130083A (en) | 1928-11-15 |
Family
ID=25710852
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH130083D CH130083A (en) | 1926-02-19 | 1927-02-14 | Process for the preparation of a violet vat dye of the 2-thionaphthene-2-indolindigo series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH130083A (en) |
-
1927
- 1927-02-14 CH CH130083D patent/CH130083A/en unknown
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