CH106430A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106430A CH106430A CH106430DA CH106430A CH 106430 A CH106430 A CH 106430A CH 106430D A CH106430D A CH 106430DA CH 106430 A CH106430 A CH 106430A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- production
- dye
- indigoid dye
- chloro
- 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
- C09B7/10—Bis-thionapthene indigos
Description
Verfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden,,dass man einen neuen indigoiden Farbstoff erhält, wenn man das 8-Chlor-1,2-thionaphthis.atin (welches erhal ten werden kann durch Kondensieren von 8- Chlo,r-l-thionaphthol mit Oxalylchlorid) mit Oxythionaphthenkarbonsii,ure kondensiert und das so ;erhaltene Produkt bromiert.
Der neue Farbstoff bildet ein rotes Pul ver, löst sich in konzentrierter Schwefelsäure mit grüner Farbe, gibt mit Hydrosulfit und Natronlauge eine goldgelbe Küpe und erzeugt auf Baumwolle Färbungen, welche nach dem Seifen violett und sehr echt werden.
<I>Beispiel:</I> In 10000 Teile Alkohol werden 248,5 Teile 8-Chlor-1,2-thionaphthis-atin und 194 Teile Oxythion.aphthenkarbonsäure eingetra gen und hierauf die Mischung längere Zeit am Rückflusskühler gekocht. Der gebildete Farbstoff wird filtriert, gewaschen und ge- troicknet. 380 Teile des so erhaltenen Farbstoffes werden bei 0 bis 5 in eine Mischung von 9000 Teilen 90 %iger,Schwefelsäure mit 144 Teilen Brom eingetragen und 12 Stunden bei gewöhnlicher Temperatur gerührt.
Hierauf wird auf Eis ausgetragen, der abgeschiedene Farbstoff filtriert und getrocknet.
Process for the production of a new indigoid dye. It has been found that a new indigoid dye is obtained if 8-chloro-1,2-thionaphthis.atin (which can be obtained by condensing 8-chloro, rl-thionaphthol with oxalyl chloride) with oxythionaphthene carboxylic acid condensed and the product thus obtained brominated.
The new dye forms a red powder, dissolves in concentrated sulfuric acid with a green color, gives a golden yellow vat with hydrosulfite and sodium hydroxide solution and creates colors on cotton that turn violet and very real after soaking.
<I> Example: </I> 248.5 parts of 8-chloro-1,2-thionaphthis-atin and 194 parts of oxythione-naphthenic acid are added to 10,000 parts of alcohol, and the mixture is then boiled on the reflux condenser for a long time. The dye formed is filtered, washed and dried. 380 parts of the dye thus obtained are introduced at 0 to 5 into a mixture of 9000 parts of 90% strength sulfuric acid with 144 parts of bromine and the mixture is stirred for 12 hours at ordinary temperature.
It is then poured onto ice, and the deposited dye is filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106430T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106430A true CH106430A (en) | 1924-09-01 |
Family
ID=25705845
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106430D CH106430A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106430A (en) |
-
1922
- 1922-12-07 CH CH106430D patent/CH106430A/en unknown
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