CH106434A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106434A CH106434A CH106434DA CH106434A CH 106434 A CH106434 A CH 106434A CH 106434D A CH106434D A CH 106434DA CH 106434 A CH106434 A CH 106434A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- dye
- green
- 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
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr.<B>100705.</B> Verfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, dass man einen neuen indigoid.en Farbstoff erhält, wenn man das 1-Brom-2,3-thionaphthisatin (welches erhal ten werden kann durch Kondensieren von 1- Brom-2-thionaphihol mit Oxalylchlorid) mit 2,3-Naphtthioindoxyl kondensiert und das so erhaltene Produkt bromiert.
Der neue Farbstoff bildet ein .grünblaues Pulver, löst sich in konzentrierter Schwefel säure mit grüner Farbe, gibt -mit Hydrosulfit und Natronlauge eine orange Küpe und er zeugt auf Baumwolle Färbungen, welche nach dem Seifen grünblau und sehr echt werden.
Beispiel: In 10000 Teilen Alkohol werden 293 Teile 1-Brom-2,1-thionaphthis.atin und 200 Teile 2,3-Naphththioindoxyl eingetragen und hierauf die Mischung längere Zeit am Rück ilusskühler gekocht. Der gebildete Farbstoff wird filtriert, gewaschen und getrocknet.
380 Teile des so erhaltenen Farbstoffes werden bei 0 bis 5 in eine Mischung von 9000 Teilen 98 %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.
<B> Additional patent </B> to main patent no. <B> 100705. </B> Process for the production of a new indigoid dye. It has been found that a new indigoid.en dye is obtained if 1-bromo-2,3-thionaphthisatin (which can be obtained by condensing 1-bromo-2-thionaphihol with oxalyl chloride) with 2,3- Naphthioindoxyl condenses and the product thus obtained is brominated.
The new dye forms a green-blue powder, dissolves in concentrated sulfuric acid with a green color, gives an orange vat with hydrosulphite and sodium hydroxide solution and it produces dyeings on cotton that turn green-blue and very real after soaking.
Example: 293 parts of 1-bromo-2,1-thionaphthis.atin and 200 parts of 2,3-naphththioindoxyl are added to 10,000 parts of alcohol and the mixture is then boiled for a long time on the reflux cooler. 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 98% 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 | ||
CH106434T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106434A true CH106434A (en) | 1924-09-01 |
Family
ID=25705849
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106434D CH106434A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106434A (en) |
-
1922
- 1922-12-07 CH CH106434D patent/CH106434A/en unknown
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