CH232297A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH232297A CH232297A CH232297DA CH232297A CH 232297 A CH232297 A CH 232297A CH 232297D A CH232297D A CH 232297DA CH 232297 A CH232297 A CH 232297A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- olive
- melt
- green
- methoxy
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/2409—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position not provided for in one of the sub groups C09B5/26 - C09B5/62
- C09B5/2436—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position not provided for in one of the sub groups C09B5/26 - C09B5/62 only nitrogen-containing hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paper (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 228649. Verfahren zur Herstellung eines ILüpenfarbstoffes. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Herstellung eines neuen Küpenfarbstoffes, welches darin besteht, dass man die durch Kondensation von 4-Brom- 3-methoxy -1.8 - chinoylen-naphtalin und 1- Amino-4-methoxy-anthrachinon erhältliche Verbindung von der Zusammensetzung:
EMI0001.0011
in einer Alkalischmelze erhitzt.
Man kann die Schmelze auch in Gegen wart von Lösungs- oder Verdünnungsmitteln, wie z. B. Äthylalkohol und Äthanolamin durchführen.
<I>Beispiel:</I> 10 Gewichtsteile der durch Kondensation von 4-Brom-3-methoxy-1..8-chinoylen-naph- ta.lin und 1-Amino-4-metlioxy-anthracliinon er hältlichen Verbindung, die ein in konzentrier ter Schwefelsäure mit blauer Farbe lösliches dunkelviolettes Pulver darstellt, werden so lange in einer Schmelze aus 100 Gewichts teilen Kaliumhydroxyd, 90 Volumteilen Äthylalkohol und 10 Volumteilen Xtlia- nolamin am Rückflusskühler unter Rüh ren erhitzt,
bis eine Probe mit konz. Schwe felsäure nurmehr eine trübolivbraune Lösung ergibt, aus der sich beim Eingiessen in Was ser der Farbstoff in blauen Flocken als Sul fat abscheidet. Nach etwa 11/2- bis ?stündiger Schmelzdauer gibt man die Schmelze in Was ser. Die zum Teil noch in Form der Leuko- verbindung vorliegende neue Verbindung wird durch Einleiten von Luft zum Farb- stoff oxydiert. Er wird mit heissem Wasser neutral gewaschen, wobei entstandene Neben produkte mit rotbrauner Farbe in Lösung gehen.
Zur vollständigen Entfernung der letzteren extrahiert man die noch feuchte Paste mit Alkohol.
Der Farbstoff stellt ein dunkelolivgrünes Pulver dar. Er kristallisiert aus 1-Chlor- naphtalin in verfilzten, langen, olivgrünen Nädelchen, die sich in konzentrierter Schwe felsäure mit gelbbrauner Farbe lösen. Beim Eingiessen dieser Lösung in Wasser fallen violette Flocken aus. Der Farbstoff färbt Baumwolle aus grünoliver Küpe in Khaki- tönen von guten Echtheiten.
Additional patent to main patent no. 228649. Process for the production of an I-pulp dye. The subject of this additional patent is a process for the production of a new vat dye, which consists in removing the compound obtainable by condensation of 4-bromo-3-methoxy -1.8-quinoylen-naphthalene and 1-amino-4-methoxy-anthraquinone from the composition :
EMI0001.0011
heated in an alkali melt.
You can also use the melt in the presence of solvents or diluents, such as. B. Perform ethyl alcohol and ethanolamine.
<I> Example: </I> 10 parts by weight of the compound obtainable by condensation of 4-bromo-3-methoxy-1..8-quinoylen-naphtha.lin and 1-amino-4-metlioxy-anthracliinone which represents a dark violet powder soluble in concentrated sulfuric acid with a blue color, are heated in a melt of 100 parts by weight of potassium hydroxide, 90 parts by volume of ethyl alcohol and 10 parts by volume of xtlienolamine on the reflux condenser with stirring,
until a sample with conc. Sulfuric acid only results in a cloudy olive-brown solution, from which, when poured into water, the dye is deposited in blue flakes as sulphate. After about 11/2 to 1 hour melting time, the melt is poured into water. The new compound, some of which is still in the form of the leuco compound, is oxidized to the dye by the introduction of air. It is washed neutral with hot water, with the resulting by-products dissolving with a red-brown color.
To completely remove the latter, the paste, which is still moist, is extracted with alcohol.
The dye is a dark olive-green powder. It crystallizes from 1-chloronaphthalene in matted, long, olive-green needles that dissolve in concentrated sulfuric acid with a yellow-brown color. When this solution is poured into water, purple flakes precipitate. The dye dyes cotton from a green-olive vat in khaki tones with good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE232297X | 1941-08-06 | ||
CH228649T | 1942-07-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH232297A true CH232297A (en) | 1944-05-15 |
Family
ID=25727235
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH232297D CH232297A (en) | 1941-08-06 | 1942-07-21 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH232297A (en) |
-
1942
- 1942-07-21 CH CH232297D patent/CH232297A/en unknown
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