CH107134A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH107134A CH107134A CH107134DA CH107134A CH 107134 A CH107134 A CH 107134A CH 107134D A CH107134D A CH 107134DA CH 107134 A CH107134 A CH 107134A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- production
- blue
- indigoid 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
- C09B7/12—Other thionaphthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Znsatzpaf;ent' zum Hauptpatent Nr. 100705. Verfahren zur Herstellung eines indigoiden Farbstoffes. Es wurde gefunden, dass man einen indigoiden Farbstoff herstellen kann, wenn man das Acenaphthenchinon mit 2,3-Naplitli- thioindoxyl kondensiert und den so erhalte nen Farbstoff bromiert. Der-Farbstoff stellt ein blaurotes Pulver dar, das sich in kon zentrierter Schwefelsäure mit grüner Farbe löst;
er gibt mit Hydrosulfit und Natron lauge eine orangebraune Küpe, aus der Baum wolle in blauroten Tönen von guter Echtheit gefärbt wird.
Beispiel: 182 Teile Acenaphthenchinon und 200 Teile 2,3-Naphththioindoxyl werden in 5000 Teilen Alkohol suspendiert und zum Sieden erhitzt. Dann gibt man 5 Teile konzentrierte Salzsäure zu. Nach kurzem Kochen ist die Kondensation beendigt. Es wird heiss fil triert, gewaschen und getrocknet.
366 Teile des so erhaltenen Farbstoffes werden in 6000 Teile Nitrobenzol eingetra gen und mit 176 Teilen Brom versetzt. Während 24 Stunden wird die Reaktions masse sich selbst überlassen und hierauf die- Temperatur im Verlaufe mehrerer Stunden auf<B>160'</B> gesteigert. Nach dem Erkalten wird abfiltriert und der Filterrückstand mit Alko hol gewaschen und getrocknet.
Znsatzpaf; ent 'to main patent no. 100705. Process for the production of an indigoid dye. It has been found that an indigoid dye can be produced if the acenaphthenquinone is condensed with 2,3-naplitlithioindoxyl and the dye obtained in this way is brominated. The dye is a blue-red powder that dissolves in concentrated sulfuric acid with a green color;
he gives an orange-brown vat with hydrosulfite and sodium hydroxide solution, from which cotton is dyed in blue-red shades of good fastness.
Example: 182 parts of acenaphthenquinone and 200 parts of 2,3-naphththioindoxyl are suspended in 5000 parts of alcohol and heated to the boil. Then 5 parts of concentrated hydrochloric acid are added. After a short boil, the condensation is over. It is filtered hot, washed and dried.
366 parts of the dye thus obtained are introduced into 6000 parts of nitrobenzene and 176 parts of bromine are added. The reaction mass is left to its own devices for 24 hours and the temperature is then increased to 160 'over the course of several hours. After cooling, it is filtered off and the filter residue is washed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH107134T | 1923-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH107134A true CH107134A (en) | 1924-10-01 |
Family
ID=25705874
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH107134D CH107134A (en) | 1922-11-18 | 1923-03-29 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH107134A (en) |
-
1923
- 1923-03-29 CH CH107134D patent/CH107134A/en unknown
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