CH116085A - Process for the production of an indigoid dye of the anthracene series. - Google Patents
Process for the production of an indigoid dye of the anthracene series.Info
- Publication number
- CH116085A CH116085A CH116085DA CH116085A CH 116085 A CH116085 A CH 116085A CH 116085D A CH116085D A CH 116085DA CH 116085 A CH116085 A CH 116085A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- anthracene series
- indigoid dye
- dye
- anthracene
- 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
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden Farbstoffes der Anthracenreihe. Es wurde gefunden, dass man einen in- digoiden Farbstoff der Anthracenreihe erhält, wenn man ein Anil des 2,3-Anthraaen- thiaisatins mit Oxythionaphthenkarbonsäure kondensiert. Der Farbstoff bildet ein grün schwarzes Pulver,
das sich in Schwefel säure mit brauner Farbe löst und eine vio- lettbraune Küpe gibt; aus welcher Baum wolle grün gefärbt wird. <I>Beispiel</I> 19 Teile des p-Dimethylämi.noanils des 2,3-Anthra;centhioisatins werden mit 10 Tei len Oxythionaphthenkarbonsäure und 500 Teilen Pyridin oder Trichlorbenzol zwei Stunden unter Rückfluss gekocht. Der aus geschiedene Farbsto-ff wird abgesaugt, ge waschen und getrocknet.
Die Reaktion verläuft nach folgender Gleichunz:
EMI0001.0026
Process for the production of an indigoid dye of the anthracene series. It has been found that an indigo dye of the anthracene series is obtained if an anil of 2,3-anthracene thiaizatin is condensed with oxythionaphthene carboxylic acid. The dye forms a green black powder,
which dissolves in sulfuric acid with a brown color and gives a violet brown vat; which tree wool is colored green. <I> Example </I> 19 parts of p-Dimethylämi.noanil des 2,3-Anthra; centhioisatins are refluxed with 10 parts of oxythionaphthenecarboxylic acid and 500 parts of pyridine or trichlorobenzene for two hours. The separated dye is filtered off with suction, washed and dried.
The reaction proceeds according to the following equation:
EMI0001.0026
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103649T | 1923-01-24 | ||
CH116085T | 1924-06-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH116085A true CH116085A (en) | 1926-08-02 |
Family
ID=25706540
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH116085D CH116085A (en) | 1923-01-24 | 1924-06-21 | Process for the production of an indigoid dye of the anthracene series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH116085A (en) |
-
1924
- 1924-06-21 CH CH116085D patent/CH116085A/en unknown
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