CH264197A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH264197A CH264197A CH264197DA CH264197A CH 264197 A CH264197 A CH 264197A CH 264197D A CH264197D A CH 264197DA CH 264197 A CH264197 A CH 264197A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- vat
- brown
- vat dye
- 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
- 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
- C09B5/26—Carbazoles of the anthracene series
- C09B5/28—Anthrimide carbazoles
-
- 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
- C09B5/26—Carbazoles of the anthracene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 257722. Verfahren zur Herstellung eines Küpenfarbstoffes. Es wurde gefunden, dass ein wertvoller Küpenfarbstoff hergestellt werden kann, wenn man das Kondensationsprodukt aus 1 Mol 3',6'-Dihalogen-monophthaloyl-pyren und 2 Mol 5-Amino-1,1'-dianthrimid der Formel
EMI0001.0009
mit carbazolierenden Mitteln behandelt.
Der neue Farbstoff ist ein braunschwarzes Pulver, das sich in konz. Schwefelsäure mit schmutzig violetter Farbe löst und Baumwolle aus rotbrauner Küpe in gelbstichig braunen Tönen färbt.
<I>Beispiel:</I> 30 Teile Aluminiumchlorid und 3,6 Teile Kochsalz werden innig vermischt und bei 1400 verschmolzen. Nun werden bei 140 bis 1450 1,5 Teile des Kondensationsproduktes aus 3',6'-Dichlor-3,4-monophthaloyl-pyren und 5- Amino-1,1'-dianthrimid eingetragen und zwei Stunden bei 165 bis 1680 gerührt. Nach dem Austragen in Eis und Wasser wird mit ver dünnter Schwefelsäure angesäuert und mit 0,9 Teilen Natriumdichromat bei gewöhnlicher Temperatur nachoxydiert.
Das hier verwendete Kondensationspro dukt kann aus 1 Mol 3',6'-Dichlor-3,4-mono- phthaloyl-pyren und 2 Mol 5-Amino-1,1'-di- anthrimid unter Zusatz von Kupfersalzen in siedendem Nitrobenzol in üblicher Weise her gestellt werden.
<B> Additional patent </B> to main patent no. 257722. Process for the production of a vat dye. It has been found that a valuable vat dye can be prepared if the condensation product of 1 mole of 3 ', 6'-dihalo-monophthaloyl-pyrene and 2 moles of 5-amino-1,1'-dianthrimide of the formula
EMI0001.0009
treated with carbazolating agents.
The new dye is a brown-black powder, which is in conc. Sulfuric acid dissolves with a dirty purple color and dyes cotton from a reddish brown vat in yellowish brown tones.
<I> Example: </I> 30 parts of aluminum chloride and 3.6 parts of table salt are intimately mixed and fused at 1400. 1.5 parts of the condensation product of 3 ', 6'-dichloro-3,4-monophthaloyl-pyrene and 5-amino-1,1'-dianthrimide are then introduced at 140 to 1450 and the mixture is stirred at 165 to 1680 for two hours. After pouring into ice and water, the mixture is acidified with dilute sulfuric acid and post-oxidized with 0.9 parts of sodium dichromate at ordinary temperature.
The condensation product used here can be prepared from 1 mole of 3 ', 6'-dichloro-3,4-monophthaloyl-pyrene and 2 moles of 5-amino-1,1'-di-anthrimide with the addition of copper salts in boiling nitrobenzene in the usual way Way to be made.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH257722T | 1946-03-29 | ||
CH264197T | 1947-02-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH264197A true CH264197A (en) | 1949-09-30 |
Family
ID=25730126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH264197D CH264197A (en) | 1946-03-29 | 1947-02-19 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH264197A (en) |
-
1947
- 1947-02-19 CH CH264197D patent/CH264197A/en unknown
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