AT64978B - Process for the preparation of selenium cyanides and selenophenols of the anthraquinone series. - Google Patents
Process for the preparation of selenium cyanides and selenophenols of the anthraquinone series.Info
- Publication number
- AT64978B AT64978B AT64978DA AT64978B AT 64978 B AT64978 B AT 64978B AT 64978D A AT64978D A AT 64978DA AT 64978 B AT64978 B AT 64978B
- Authority
- AT
- Austria
- Prior art keywords
- selenium
- cyanides
- selenophenols
- preparation
- anthraquinone series
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
Es wurde gefunden, dass beim Erhitzen von Diazoseleneyaniden der Anthrachinonreihe, ohne dass die Zufügung einer Kontaktsubstanz (Kupfer oder Kupferoxydulsalze) erforderlich ist, die Selencyangruppe in glatt verlaufender Reaktion unter Abspaltung von Stickstoff in den Kern tritt :
EMI1.2
Die Selencyanide lassen sich durch die für Rhodanide bekannten Reagenzien, wie z. B. durch alkoholisches Kali oder Natron, zu Selenophenolen aufspalten.
Beispiel : 2.2 kg I-Aminoanthrachinon werden in bekannter Weise in konzentrierter Schwefelsaun mit Nitrosylscbwefelsäure diazotiert. Das beim Verdünnen mit Eis aus- gefällte Diazosulfat wird abfiltriert, in Wasser gelöst und mit einer wässerigen Lösung von 1.5 kg Selcncyankalium versetzt. Es fällt hiebei ein rotes Diaxoselencyanid ans, welches schon in der Kälte einen Teil des Stickstoffs verliert. Zur Yollcndung der Reaktion
EMI1.3
und anderen.
Analog verfahrt man bei Verwendung des ss-Aminoanthrachinons, der DiaminoanthrachinonederDerivateallerdieserVerbindungen.
Die neuen Stoffe sollen zur Herstellung von Farbstoffen und Heilmitteln Verwendung finden.
PATENT-ANSPRCT ('HE :
1. Verfahren zur Darstellung von Selencyaniden der Anthrachinonreihe, darin bestehend, dass Diazoselcneyanide verkocht werden.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
EMI1.1
It has been found that when diazoselene anides of the anthraquinone series are heated without the addition of a contact substance (copper or copper oxide salts), the selenium cyanide group enters the core in a smooth reaction with elimination of nitrogen:
EMI1.2
The selenium cyanides can be prepared by the reagents known for rhodanides, such as. B. by alcoholic potash or soda, split to selenophenols.
Example: 2.2 kg of I-aminoanthraquinone are diazotized in a known manner in concentrated sulfuric acid with nitrosylsulfuric acid. The diazo sulfate precipitated on dilution with ice is filtered off, dissolved in water and mixed with an aqueous solution of 1.5 kg of potassium cyanide. A red diaxoselenium cyanide falls, which loses part of the nitrogen even in the cold. To complete the reaction
EMI1.3
and others.
The procedure is analogous when using the ß-aminoanthraquinone, the diaminoanthraquinone of the derivatives of all these compounds.
The new substances are to be used for the manufacture of dyes and medicines.
PATENT-ANSPRCT ('HE:
1. Process for the preparation of selenium cyanides of the anthraquinone series, consisting in boiling diazoselcneyanides.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE64978X | 1912-01-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT64978B true AT64978B (en) | 1914-05-25 |
Family
ID=5632655
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT64978D AT64978B (en) | 1912-01-24 | 1913-01-11 | Process for the preparation of selenium cyanides and selenophenols of the anthraquinone series. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT64978B (en) |
-
1913
- 1913-01-11 AT AT64978D patent/AT64978B/en active
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