CH121569A - Process for the preparation of a new benzanthrone derivative. - Google Patents
Process for the preparation of a new benzanthrone derivative.Info
- Publication number
- CH121569A CH121569A CH121569DA CH121569A CH 121569 A CH121569 A CH 121569A CH 121569D A CH121569D A CH 121569DA CH 121569 A CH121569 A CH 121569A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- preparation
- dyes
- silk
- benzanthrone derivative
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines neuen Benzanthronderivates. Es wurde gefunden, dass man zu einem wertvollen Derivat des Benzanthrons gelangt, wenn man Bz-1-Nitrobenzanthron mit einem Alkalisulfit behandelt. Die neue Verbindung ist wasserlöslich und stellt eine Sulfosäure des Aminobenzanthrons dar, welcher wahr scheinlich die Formel:
EMI0001.0007
zukommt.
Beispiel: 100 Teile Bz-1-Nitrobenzanthron werden in fein verteilter Form, zweckmässig als Paste, mit 1000 Teilen technischer Natrium- bisulfitlösung so lange am Rückflusskühler gekocht, bis alles oder fast alles umgesetzt ist. Nach dem Verdünnen mit heissem Wasser trennt man von unangegriffenem Ausgangs material durch Filtrieren. Die Lösung wird alsdann angesäuert, die schweflige Säure durch kurzes Kochen vertrieben und das Re aktionsprodukt durch Zugabe von Kochsalz zur Abscheidung gebracht.
Der neue Körper stellt ein dunkelrotes Pulver dar, welches sich in heissem Wasser leicht mit roter Farbe auflöst. Die Lösungs farbe in konzentrierter Schwefelsäure ist bräunlichgelb mit schwacher Fluoreszenz. Er stellt an sich schon einen Farbstoff dar und gibt zum Beispiel auf Wolle, Seide, Azetat- seide leuchtend brote Färbungen. Daneben kann der ,neue Stoff als. Ausgangsmaterial für die Darstellung weiterer Farbstoffe die nen.
Process for the preparation of a new benzanthrone derivative. It has been found that a valuable derivative of benzanthrone is obtained if Bz-1-nitrobenzanthrone is treated with an alkali sulfite. The new compound is water-soluble and is a sulfonic acid of aminobenzanthrone, which probably has the formula:
EMI0001.0007
comes to.
Example: 100 parts of Bz-1-nitrobenzanthrone are finely divided, conveniently as a paste, boiled with 1000 parts of technical sodium bisulfite solution on the reflux condenser until everything or almost everything has been converted. After dilution with hot water, unaffected starting material is separated by filtration. The solution is then acidified, the sulphurous acid expelled by brief boiling and the reaction product is made to separate out by adding common salt.
The new body is a dark red powder that dissolves easily with red color in hot water. The solution color in concentrated sulfuric acid is brownish-yellow with weak fluorescence. In itself it is a dye and gives bright, bread dyes on wool, silk and acetate silk, for example. In addition, the new substance can be used as a. Starting material for the preparation of other dyes.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE121569X | 1925-06-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH121569A true CH121569A (en) | 1927-07-16 |
Family
ID=5656977
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH121569D CH121569A (en) | 1925-06-27 | 1926-06-18 | Process for the preparation of a new benzanthrone derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH121569A (en) |
-
1926
- 1926-06-18 CH CH121569D patent/CH121569A/en unknown
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