CH106427A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106427A CH106427A CH106427DA CH106427A CH 106427 A CH106427 A CH 106427A CH 106427D A CH106427D A CH 106427DA CH 106427 A CH106427 A CH 106427A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- indigoid dye
- dye
- parts
- 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
<B>Zusatzpatent</B> zuin Hauptpatent Nr. 100705. Verfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, dass ein neuer, wert voller indigoider Farbstoff entsteht, wenn man das 1,2-Nap:hththioindoxyl mit a-Isatin- anilid kondensiert und das so erhaltene Pro dukt bromiert.
Der neue Faserstoff stellt ein violettes Pulver dar, das sich in Schwefelsäure mit grünblauer Farbe löst. Er färbt Baumwolle aus goldgelber Küpe in blauvioletten Tönen, die beim Seifen in ein Heliotrop von guter Echtheit übergehen.
Beispiel: 200 Teile 1,2-Naphththioindoxyl und 222 Teile a-Isatinanilid werden in 4000 Teilen Alkohö#l suspendiert und nach Zugabe von 5 Teilen Soda zum Sieden erhitzt. Nach kurzem Kochen ist die Kondensation beendigt. Der in sehen guter Ausbeute abgeschiedene Farbstoff wird filtriert, gewaschen und getrocknet.
329 Teile des so erhaltenen Farbstoffes werden in 6000 Teilen Nitrobenzol eingetra- gen und mit<B>176</B> Teilen Brom versetzt. Wäh rend 24 Stunden wird die Reaktionsmasse sich selbst überlassen und hierauf während 20 Stunden die Temperatur langsam bis 120' gesteigert. Nach dem Erkalten wird abfil- triert und der Filterrückstand mit Alkohol gründlich nachgewa.schen und getrocknet.
<B> Additional patent </B> to main patent no. 100705. Process for the production of a new indigoid dye. It has been found that a new, valuable indigoid dye is formed if the 1,2-Nap: ththioindoxyl is condensed with α-isatin anilide and the product thus obtained is brominated.
The new fiber is a purple powder that dissolves in sulfuric acid with a green-blue color. It dyes cotton from a golden yellow vat in blue-violet tones, which change into a heliotrope of good fastness when soaped.
Example: 200 parts of 1,2-naphththioindoxyl and 222 parts of α-isatin anilide are suspended in 4000 parts of alcohol and, after addition of 5 parts of soda, are heated to the boil. After a short boil, the condensation is over. The dyestuff deposited in good yield is filtered, washed and dried.
329 parts of the dye thus obtained are introduced into 6000 parts of nitrobenzene, and 176 parts of bromine are added. During 24 hours the reaction mass is left to its own devices and the temperature is then slowly increased to 120 'over 20 hours. After cooling, it is filtered off and the filter residue is washed thoroughly with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106427T | 1923-04-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106427A true CH106427A (en) | 1924-09-01 |
Family
ID=25705842
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106427D CH106427A (en) | 1922-11-18 | 1923-04-10 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106427A (en) |
-
1923
- 1923-04-10 CH CH106427D patent/CH106427A/en unknown
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