CH190037A - Process for the production of an anthraquinone derivative. - Google Patents
Process for the production of an anthraquinone derivative.Info
- Publication number
- CH190037A CH190037A CH190037DA CH190037A CH 190037 A CH190037 A CH 190037A CH 190037D A CH190037D A CH 190037DA CH 190037 A CH190037 A CH 190037A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- carried out
- anthraquinone derivative
- color
- derivative
- Prior art date
Links
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Anthraehinonderivates. Gegenstand vorliegender Erfindung ist ein Verfahren zur Herstellung eines Anthra- chinonderivates, durch Einwirkung von Ha logenwasserstoff abspaltenden Mitteln auf 1 . 2'- Naphthylamino - 2 - bromauthrachinon. Als Halogenwasserstoff abspaltendes Mittel sei Kaliumcarbonat oder Alkalihydroxyd ge nannt.
Die Reaktion wird zweckmässig in einem Lösungsmittel wie Nitrobenzol, Kre- sol, Benzylalkohol oder einem aliphatischen Alkohol wie N-Butylalkohol oder Amyl- alkohol oder Glykol durchgeführt. Die Ab spaltung von Halogenwasserstoff kann durch Zusatz kleiner Mengen Kupfer oder eines Kupfersalzes beschleunigt werden.
Das erhältliche Umsetzungsprodukt ist orange gefärbt und löst sich in konzentrier ter Schwefelsäure mit zunächst grünlich blauer, dann rein blauer Farbe. Es soll als Küpenfarbstoff und als Zwischenprodukt für die Herstellung anderer Verbindungen (z. B. Sulfierungsprodukte oder saure Schwefel- Säureester der Leukoverbindungen) ange wandt werden.
<I>Beispiel:</I> 10 Gewichtsteile 1.2'-Naphthylamino- 2,bromanthrachinön und 2,5 Gewichtsteile Kaliumcarbonat werden in 100 Gewichts teilen siedenden Nitrobenzols ungefähr 3 Stunden gerührt. Die nach dem Erkalten isolierte Abscheidung besteht aus orangen Kristallen, die sich in konzentrierter Schwe felsäure erst mit grünstichig blauer, bald reiner blau werdenden Farbe lösen. Wahr scheinlich liegt das 1. 2-Phthaloyl-5. ,6 benzoearbazol vor.
Process for the preparation of an anthraquinone derivative. The present invention relates to a process for the production of an anthrachinone derivative by the action of agents which split off hydrogen halide on 1. 2'-naphthylamino-2-bromoauthraquinone. Potassium carbonate or alkali metal hydroxide may be mentioned as an agent which splits off hydrogen halide.
The reaction is expediently carried out in a solvent such as nitrobenzene, creole, benzyl alcohol or an aliphatic alcohol such as n-butyl alcohol or amyl alcohol or glycol. The elimination of hydrogen halide can be accelerated by adding small amounts of copper or a copper salt.
The available reaction product is orange in color and dissolves in concentrated sulfuric acid with an initially greenish blue, then a purely blue color. It should be used as a vat dye and as an intermediate for the production of other compounds (e.g. sulphonation products or acidic sulfuric acid esters of leuco compounds).
<I> Example: </I> 10 parts by weight of 1,2'-naphthylamino-2, bromanthraquinone and 2.5 parts by weight of potassium carbonate are stirred in 100 parts by weight of boiling nitrobenzene for about 3 hours. The deposit, isolated after cooling, consists of orange crystals that dissolve in concentrated sulfuric acid first with a greenish blue color that soon becomes pure blue. Probably the 1. 2-phthaloyl-5. , 6 benzoearbazole before.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE190037X | 1934-08-01 | ||
CH186555T | 1935-07-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH190037A true CH190037A (en) | 1937-03-31 |
Family
ID=25721383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH190037D CH190037A (en) | 1934-08-01 | 1935-07-31 | Process for the production of an anthraquinone derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH190037A (en) |
-
1935
- 1935-07-31 CH CH190037D patent/CH190037A/en unknown
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