CH139373A - Process for the preparation of 1,4-Dioxy-6-methyl-8-chlorobenzo-thiophanthrenequinone. - Google Patents
Process for the preparation of 1,4-Dioxy-6-methyl-8-chlorobenzo-thiophanthrenequinone.Info
- Publication number
- CH139373A CH139373A CH139373DA CH139373A CH 139373 A CH139373 A CH 139373A CH 139373D A CH139373D A CH 139373DA CH 139373 A CH139373 A CH 139373A
- Authority
- CH
- Switzerland
- Prior art keywords
- methyl
- chlorobenzo
- dioxy
- preparation
- thiophanthrenequinone
- Prior art date
Links
Landscapes
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von 1.4-Dioxy-6-methyl-8-chlorbenzo-thiophanthrenchinon. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung des 1.4-Dioxy-6- methyl-8-chlorbenzo-thiophanthrenchinons von folgender Formel:
EMI0001.0004
dadurch gekennzeichnet, dass man 5-Chlor-7- methyl-thionaphten-2.3-dicarbonsäureanhydrid mit Hydrochinon in Gegenwart eines sauren Kondensationsmittels kondensiert. Die erhal tene Verbindung soll zur Herstellung von Farbstoffen Verwendung finden.
Beispiel: Ein Gemisch von 25 Gewichtsteilen 5- Chlor- 7-methylthionaphten-2 . 3-dicarbonsäure- anhydrid und 12 Gewichtsteilen Hydrochinon wird bei 180 in eine Schmelze von 20 Ge wichtsteilen Kochsalz und 100 Gewichtsteilen Aluminiumchlorid unter Rühren eingetragen, die Temperatur auf 190 gesteigert und wäh rend 5 Stunden gehalten. Dann wird mit Eis und Salzsäure zersetzt und aufgearbeitet.
Das entstandene 1.4-Dioxy-6-methyl-8-chlor- benzo-thiophanthrenchinon:
EMI0001.0018
kann über die Diacetylverbindung oder durch Umkristallisieren aus Pyridin gereinigt wer den. Die Verbindung schmilzt bei 291L-292 und kristallisiert in federartigen Nadeln.
Process for the preparation of 1,4-Dioxy-6-methyl-8-chlorobenzo-thiophanthrenequinone. The subject of this additional patent is a process for the preparation of 1,4-dioxy-6-methyl-8-chlorobenzo-thiophanthrenequinone with the following formula:
EMI0001.0004
characterized in that 5-chloro-7-methyl-thionaphthene-2,3-dicarboxylic anhydride is condensed with hydroquinone in the presence of an acidic condensing agent. The compound obtained is intended to be used for the production of dyes.
Example: A mixture of 25 parts by weight of 5-chloro-7-methylthionaphten-2. 3-dicarboxylic anhydride and 12 parts by weight of hydroquinone is added at 180 to a melt of 20 parts by weight of table salt and 100 parts by weight of aluminum chloride with stirring, the temperature is increased to 190 and held during 5 hours. Then it is decomposed and worked up with ice and hydrochloric acid.
The resulting 1,4-dioxy-6-methyl-8-chlorobenzo-thiophanthrenequinone:
EMI0001.0018
can be purified via the diacetyl compound or by recrystallization from pyridine. The compound melts at 291L-292 and crystallizes in feather-like needles.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE139373X | 1927-09-07 | ||
CH137740T | 1928-08-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH139373A true CH139373A (en) | 1930-04-15 |
Family
ID=25713039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH139373D CH139373A (en) | 1927-09-07 | 1928-08-16 | Process for the preparation of 1,4-Dioxy-6-methyl-8-chlorobenzo-thiophanthrenequinone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH139373A (en) |
-
1928
- 1928-08-16 CH CH139373D patent/CH139373A/en unknown
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