CH263858A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH263858A CH263858A CH263858DA CH263858A CH 263858 A CH263858 A CH 263858A CH 263858D A CH263858D A CH 263858DA CH 263858 A CH263858 A CH 263858A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- vat
- dye
- vat dye
- brown
- 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
- C09B5/34—Anthraquinone acridones or thioxanthrones
- C09B5/38—Compounds containing acridone and carbazole rings
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 257722. Verfahren zur Herstellung eines Küpenfarbatoffes. Es wurde gefunden, dass ein wertvoller Küpenfarbstoff hergestellt werden kann, wenn man das Kondensationsprodukt aus 1 Mol 3',6'-Diehl.or-monophthaloyl-pyrenolin und 2 Mol 4-Amino-1,1'-dianthrimid der Formel
EMI0001.0007
mit earbazolierenden Mitteln behandelt.
Der neue Farbstoff ist ein dunkles Pulver, das sich in konz. Schwefelsäure mit brauner Farbe löst -und Baumwolle aus brauner Küpe in farbstarken, grünstichigen Olivtönen färbt.
Beisviel: 1,5 Teile des aus 1 Mol 3',6'-Dichlor-mono- phthaloyl-pyrenolin und 2 Mol 4-Amino- anthrachinon-1,1'-dianthrimid durch Erhitzen in Nitrobenzol unter Kupferacetatzusatz er hältlichen Kondensationsproduktes werden bei 1000 in eine Schmelze von 20 Teilen Alumi niumchlorid und 50 Teilen trockenem Pyridin eingetragen und die Temperatur auf 140 bis 1420 erhöht,
wobei eine kleine Menge Pyridin abdestilliert. Dann wird zwei Stunden bei 140 bis 1420 gerührt und die Reaktionsmasse in Wasser- ausgetragen, mit Natronlauge phenol- phthalein-alkalisch gestellt und mit Natrium- hydrosulfit verküpt. Nach dem Abfiltrieren von wenig Unlöslichem wird der Farbstoff mit Luft ausgeblasen, abfiltriert, ausgewa schen und getrocknet.
Additional patent to main patent No. 257722. Process for the production of a vat colorant. It has been found that a valuable vat dye can be produced if the condensation product of 1 mole of 3 ', 6'-Diehl.or-monophthaloyl-pyrenoline and 2 moles of 4-amino-1,1'-dianthrimide of the formula
EMI0001.0007
treated with earbazolating agents.
The new dye is a dark powder that is in conc. Sulfuric acid with a brown color dissolves and dyes cotton from a brown vat in strong, greenish olive tones.
For example: 1.5 parts of the condensation product obtained from 1 mole of 3 ', 6'-dichloro-monophthaloyl-pyrenoline and 2 moles of 4-aminoanthraquinone-1,1'-dianthrimide by heating in nitrobenzene with the addition of copper acetate are obtained at 1000 entered in a melt of 20 parts of aluminum chloride and 50 parts of dry pyridine and increased the temperature to 140 to 1420,
with a small amount of pyridine distilling off. The mixture is then stirred for two hours at 140 to 1420 and the reaction mixture is poured into water, made phenol-phthalein-alkaline with sodium hydroxide solution and vat with sodium hydrosulfite. After filtering off little insoluble matter, the dye is blown out with air, filtered off, washed out and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH257722T | 1946-03-29 | ||
CH263858T | 1946-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH263858A true CH263858A (en) | 1949-09-15 |
Family
ID=25730125
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH263858D CH263858A (en) | 1946-03-29 | 1946-03-29 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH263858A (en) |
-
1946
- 1946-03-29 CH CH263858D patent/CH263858A/en unknown
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