CH159301A - Process for the preparation of a new condensation product of the anthraquinone series. - Google Patents
Process for the preparation of a new condensation product of the anthraquinone series.Info
- Publication number
- CH159301A CH159301A CH159301DA CH159301A CH 159301 A CH159301 A CH 159301A CH 159301D A CH159301D A CH 159301DA CH 159301 A CH159301 A CH 159301A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- condensation product
- yellow
- anthraquinone series
- nitrobenzene
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Terfahren zur Darstellung eines neuen Kondensationsproduktes der Antbrachinonreihe. Das vorliegende Verfahren betrifft die Darstellung von Carbaethoxy-4-methoxyan- thrapyridon und ist dadurch gekennzeichnet, dass man 1-Amino-4-methoxy-anthrachinon mit Malonester in Gegenwart von Natrium acetat und Nitrobenzol erhitzt. Die neue Ver bindung soll zur Darstellung von Farbstoffen Verwendung finden.
<I>Beispiel:</I> Man erhitzt 20 Teile 1-Amino-4-methoxy- anthrachinon, 0,5 Teile . Natriumacetat, 40 Teile Malonester und 20 Teile Nitrobenzol auf 170-185 , bis die Menge des Destillats, das aus Aceton und Alkohol besteht, nicht mehr zunimmt.
Man erhält das Carbaethoxy-4-methogy- anthrapyridon als gelbe Spiesse und Prismen vom F. P. 292 C unter Zersetzung. Aus Ni trobenzol kristallisiert erhält man das Pyri- don als gelbe Spiesse und Prismen vom F. P. 298 C (Zersetzung). Das Pyridon löst sich in Schwefelsäure mit gelber Farbe, welche auf Zusatz von Borsäure orange wird.
A method for the presentation of a new condensation product of the antbrachinone series. The present process relates to the preparation of carbaethoxy-4-methoxyanothrapyridone and is characterized in that 1-amino-4-methoxy-anthraquinone is heated with malonic ester in the presence of sodium acetate and nitrobenzene. The new connection is intended to be used to represent dyes.
<I> Example: </I> 20 parts of 1-amino-4-methoxy-anthraquinone, 0.5 part, are heated. Sodium acetate, 40 parts malonic ester and 20 parts nitrobenzene to 170-185 until the amount of the distillate, which consists of acetone and alcohol, no longer increases.
The carbaethoxy-4-methogy-anthrapyridone is obtained as yellow skewers and prisms from F. P. 292 C with decomposition. Crystallized from nitrobenzene, the pyridone is obtained as yellow skewers and prisms from F. P. 298 C (decomposition). The pyridone dissolves in sulfuric acid with a yellow color, which turns orange when boric acid is added.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE159301X | 1930-07-18 | ||
CH156115T | 1931-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH159301A true CH159301A (en) | 1932-12-31 |
Family
ID=25716684
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH159301D CH159301A (en) | 1930-07-18 | 1931-07-17 | Process for the preparation of a new condensation product of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH159301A (en) |
-
1931
- 1931-07-17 CH CH159301D patent/CH159301A/en unknown
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