CH147706A - Process for the preparation of a derivative of dibenzpyrenquinone. - Google Patents
Process for the preparation of a derivative of dibenzpyrenquinone.Info
- Publication number
- CH147706A CH147706A CH147706DA CH147706A CH 147706 A CH147706 A CH 147706A CH 147706D A CH147706D A CH 147706DA CH 147706 A CH147706 A CH 147706A
- Authority
- CH
- Switzerland
- Prior art keywords
- dibenzpyrenquinone
- derivative
- preparation
- nitrobenzene
- nitrating
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Derivates des Dibenzpyrencliinons. Im Hauptpatent ist ein Verfahren zur Darstellung eines Derivates des Dibenzpyren- chinons beschrieben, bei dem Monoamino- dibenzpyrenchinori mit Benzoylchlorid behan delt wird.
Es wurde nun gefunden; dass man eben falls ein Derivat des Dibenzpyrenchinons von ähnlichen wertvollen Eigenschaften erhalten kann, wenn man Monoaminodibenzpyren- chinon, erhältlich durch Nitrieren von Dibenz- pyrenchinon von der Formel
EMI0001.0012
in Nitrobenzol mit 96 %iger Salpetersäure bei 80-100" und Reduktion des erhaltenen Nitrokörpers mit Schwefelnatriumlösung bei <B>90-1000</B> C, mit 1-Aminoanthracbinon-2-car- bonsäurechlorid behandelt.
Der neue Körper kristallisiert in feinen Nadeln, löst sich in konzentrierter Schwefel säure mit violetter Farbe und färbt Baum wolle aus blauroter Küpe in orangefarbenen Tönen von sehr guter Echtheit.
<I>Beispiel:</I> Man suspendiert 35 Teile Monoamino- dipenzpyrenchinori, dargestellt z. B. durch Reduktion des Mononiti-odibenzpyi-enchinons, welches durch Nitrieren von Dibenzpyren- chinon in Nitrobenzol mit 96 % iger Salpeter- säure erhalten wird, mit Schwefelnatrium, in 1250 Teilen Nitrobenzol,
gibt 30 Teile 1 - Aminoanthrachinon - 2 - carbonsäurechlorid hinzu und erwärmt eine kurze Zeit lang auf 190-205 0 C. Darauf lässt man erkalten, saugt ab und arbeitet in der üblichen Weise auf.
Process for the preparation of a derivative of Dibenzpyrencliinons. The main patent describes a process for the preparation of a derivative of dibenzpyrenquinone, in which monoamino dibenzpyrenchinori is treated with benzoyl chloride.
It has now been found; that one can also obtain a derivative of dibenzpyrenquinone of similar valuable properties by using monoaminodibenzpyrenquinone, obtainable by nitrating dibenzpyrenquinone of the formula
EMI0001.0012
in nitrobenzene with 96% nitric acid at 80-100 "and reduction of the resulting nitro body with sodium sulphide solution at <B> 90-1000 </B> C, treated with 1-aminoanthracbinone-2-carboxylic acid chloride.
The new body crystallizes in fine needles, dissolves in concentrated sulfuric acid with a violet color and dyes cotton from the blue-red vat in orange shades of very good fastness.
<I> Example: </I> 35 parts of monoamino-dipenzyrenchinori, shown e.g. B. by reducing the Mononiti-odibenzpyi-enchinons, which is obtained by nitrating dibenzpyrenquinone in nitrobenzene with 96% nitric acid, with sodium sulphide, in 1250 parts of nitrobenzene,
30 parts of 1-aminoanthraquinone-2-carboxylic acid chloride are added and the mixture is heated to 190-205 ° C. for a short time. It is then allowed to cool, suctioned off and worked up in the usual way.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE147706X | 1928-07-26 | ||
CH144577T | 1929-06-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH147706A true CH147706A (en) | 1931-06-15 |
Family
ID=25714486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH147706D CH147706A (en) | 1928-07-26 | 1929-06-24 | Process for the preparation of a derivative of dibenzpyrenquinone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH147706A (en) |
-
1929
- 1929-06-24 CH CH147706D patent/CH147706A/en unknown
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