CH134842A - Process for the preparation of an arylaminonaphthalene derivative. - Google Patents
Process for the preparation of an arylaminonaphthalene derivative.Info
- Publication number
- CH134842A CH134842A CH134842DA CH134842A CH 134842 A CH134842 A CH 134842A CH 134842D A CH134842D A CH 134842DA CH 134842 A CH134842 A CH 134842A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- derivative
- arylaminonaphthalene
- dioxynaphthalene
- oxybenzene
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Arylaminonaphtalinderivates. Analog dem im Hauptpatent beschriebe nen Verfahren kann man 1.5-Di-(4'-oxyphe- nylamino)-napbtalin darstellen, wenn man 1.5-Dioxynaphtalin und 4-Amino-l-oxybenzol mit Bisulfitlauge im offenen oder im Druck gefäss durch Erhitzen kondensiert.
<I>Beispiel:</I> 160 Teile 1.5-Dioxynaphtalin werden in einem verbleiten Rührkessel mit einer Lösung von 400 Teilen Alkalibisulfit in 3000 Teilen Wasser und 260 Teilen 4-Amino-l-oxybenzol unter Druck und Rühren etwa 36 Stunden auf 115-120 C erhitzt. Nach dem Abküh len des Kesselinhaltes presst man das in fei nen Kristallen ausgeschiedene 1.5-Di-(4'- oxyphenylamin)-naphtalin ab und wäscht es mit heissem Wasser. Die getrocknete Ver bindung schmilzt bei 278-280 C. Sie bildet bronzeglänzende Blättchen; eine wässerig alkalische Lösung, auf Papier aufgegossen, oxydiert sich an der Luft rotviolett. Die neue Verbindung ist ein Zwischenprodukt für die Herstellung von Farbstoffen.
Process for the preparation of an arylaminonaphthalene derivative. Analogously to the process described in the main patent, 1,5-di- (4'-oxyphenylamino) -napbtaline can be prepared if 1,5-dioxynaphthalene and 4-amino-1-oxybenzene are condensed with bisulfite liquor in an open or in a pressure vessel by heating.
<I> Example: </I> 160 parts of 1,5-dioxynaphthalene are mixed with a solution of 400 parts of alkali bisulfite in 3000 parts of water and 260 parts of 4-amino-1-oxybenzene under pressure and stirring for about 36 hours in a leaded stirred kettle. 120 C heated. After the contents of the kettle have cooled down, the 1,5-di- (4'-oxyphenylamine) -naphthalene precipitated in fine crystals is pressed off and washed with hot water. The dried compound melts at 278-280 C. It forms shiny bronze flakes; an aqueous alkaline solution, poured onto paper, oxidizes red-violet in air. The new compound is an intermediate for the manufacture of dyes.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE134842X | 1926-12-13 | ||
CH132030T | 1927-12-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH134842A true CH134842A (en) | 1929-08-15 |
Family
ID=25711751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH134842D CH134842A (en) | 1926-12-13 | 1927-12-03 | Process for the preparation of an arylaminonaphthalene derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH134842A (en) |
-
1927
- 1927-12-03 CH CH134842D patent/CH134842A/en unknown
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