CH143992A - Process for the preparation of a derivative of the anthanthrone. - Google Patents
Process for the preparation of a derivative of the anthanthrone.Info
- Publication number
- CH143992A CH143992A CH143992DA CH143992A CH 143992 A CH143992 A CH 143992A CH 143992D A CH143992D A CH 143992DA CH 143992 A CH143992 A CH 143992A
- Authority
- CH
- Switzerland
- Prior art keywords
- blue
- anthanthrone
- red
- derivative
- preparation
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Derivates des Anthanthrons. Es wurde gefunden, dass man ein wert volles Derivat des Anthanthrons erhalten kann, wenn man 1@Tonoanrinoanthanthrorr, wie es aus Anthanthron durch Nitrieren mit 95 o/oiger Salpetersäure in siedendem Nitrobenzol und Reduktion erhalten werden kann, dianotiert und die erhaltene Diazoverbindung verkocht.
Das erhaltene Monooxyanthanthron löst sich in konzentrierter Schwefelsäure mit grü ner Farbe, in Alkali mit blaugrüner Farbe und wird aus der alkalischen Lösung durch Zugabe von Säure in Form rotvioletter Flocken gefällt.
Es dient als Farbstoff oder als Zwischen produkt zur Herstellung von Farb"toffen und färbt Baumwolle aus blauroter Küpe in blau roten Tönen, die mit Alkali nach blaugrün umschlagen. <I>Beispiel:</I> 32 Teile Monoaminoanthanthron (darge stellt durch Reduktion des nach dein Verfah- des Hauptpatentes Nr.140417 erhältlichen Mo- nonitroanthanthrön werden in Schwefelsäure gelöst und in der üblichen Weise mit Nitrose (Lösung von Na0a in konzentrierter Schwe felsäure) oder Nitrit dianotiert.
Die erhaltene Diazosulfatlösung wird unter Rühren auf <B>80-900</B> C erhitzt, wobei Stickstoff entweicht. Man lässt erkalten, zersetzt mit Eis, saugt ab und trocknet.
Process for the preparation of a derivative of the anthanthrone. It has been found that a valuable derivative of anthanthrone can be obtained if 1 @ tonoanrinoanthanthrone, as can be obtained from anthanthrone by nitration with 95% nitric acid in boiling nitrobenzene and reduction, is dianotized and the diazo compound obtained is boiled off.
The monooxyanthanthrone obtained dissolves in concentrated sulfuric acid with a green color, in alkali with a blue-green color and is precipitated from the alkaline solution in the form of red-violet flakes by adding acid.
It is used as a dye or as an intermediate product for the production of dyes and dyes cotton from a blue-red vat in blue-red tones that turn blue-green with alkali Mononitroanthanthron obtainable according to your method of the main patent No. 140417 are dissolved in sulfuric acid and dianotized in the usual way with nitrous (solution of NaOa in concentrated sulfuric acid) or nitrite.
The resulting diazo sulfate solution is heated to 80-900 ° C. with stirring, nitrogen escaping. It is allowed to cool, decomposed with ice, suction filtered and dried.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE143992X | 1928-07-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH143992A true CH143992A (en) | 1930-12-15 |
Family
ID=5669993
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH143992D CH143992A (en) | 1928-07-28 | 1929-06-22 | Process for the preparation of a derivative of the anthanthrone. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH143992A (en) |
-
1929
- 1929-06-22 CH CH143992D patent/CH143992A/en unknown
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