CH140911A - Process for the preparation of a condensation product of the benzanthrone series. - Google Patents
Process for the preparation of a condensation product of the benzanthrone series.Info
- Publication number
- CH140911A CH140911A CH140911DA CH140911A CH 140911 A CH140911 A CH 140911A CH 140911D A CH140911D A CH 140911DA CH 140911 A CH140911 A CH 140911A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- chlorobenzanthrone
- condensation product
- orange
- benzanthrone series
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Kondensationsproduktes der Benzanthronreihe. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Darstellung von 2-Chlor- benzanthron von der Formel:
EMI0001.0004
welche darin besteht, dass man 1-Chlor-4- benzoylnaphtalin mit Kondensationsmitteln behandelt. Es ist vorteilhaft, die Reaktion mit einem Gemisch von Alkalichlorid und Aluminiumchlorid unter Zuführen von Sauer stoff durchzuführen. Das Endprodukt wird als Zwischenprodukt zur Herstellung von Farbstoffen verwandt.
<I>Beispiel</I> 20 Gewichtsteile 1-Chlor-4-benzoylnaph- talin (erhalten aus 1-Chlornaphtalin mit Ben- zoylchlorid nach Friedel Crafts F. P. 80 ) werden mit 200 Gewichtsteilen Natriumalu- miniumchlorid unter Zuleitung von Sauerstoff ungefähr 15 Stunden bei 120 gerührt. Beim Zersetzen der Schmelze mit Wasser erhält man olive Flocken. Nach der Reinigung zum Beispiel durch Vakuumsublimation werden 10-12 Gewichtsteile reines 2-Chlorbenzan- thron vom F. P. 200 erhalten.
EMI0001.0018
Aus Eisessig kristallisiert das so erhaltene 2-Chlorbenzanthron in gelben Nadeln. Die Lösungsfarbe in konzentrierter Schwefelsäure ist orange mit orangegelber Fluoreszenz.
Process for the preparation of a condensation product of the benzanthrone series. The subject of the present patent is a process for the preparation of 2-chlorobenzanthrone of the formula:
EMI0001.0004
which consists in treating 1-chloro-4-benzoylnaphthalene with condensing agents. It is advantageous to carry out the reaction with a mixture of alkali chloride and aluminum chloride with the addition of oxygen. The end product is used as an intermediate in the manufacture of dyes.
<I> Example </I> 20 parts by weight of 1-chloro-4-benzoylnaphthalene (obtained from 1-chloronaphthalene with benzoyl chloride according to Friedel Crafts FP 80) are mixed with 200 parts by weight of sodium aluminum chloride with the addition of oxygen for about 15 hours 120 stirred. When the melt is decomposed with water, olive flakes are obtained. After purification, for example by vacuum sublimation, 10-12 parts by weight of pure 2-chlorobenzanthrone from F. P. 200 are obtained.
EMI0001.0018
The 2-chlorobenzanthrone thus obtained crystallizes from glacial acetic acid in yellow needles. The solution color in concentrated sulfuric acid is orange with orange-yellow fluorescence.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE140911X | 1927-07-11 | ||
CH138864T | 1928-07-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH140911A true CH140911A (en) | 1930-06-30 |
Family
ID=25713243
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH140911D CH140911A (en) | 1927-07-11 | 1928-07-09 | Process for the preparation of a condensation product of the benzanthrone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH140911A (en) |
-
1928
- 1928-07-09 CH CH140911D patent/CH140911A/en unknown
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