CH128117A - Process for the preparation of Bz1-ethyl-Bz2-methylbenzanthrone. - Google Patents
Process for the preparation of Bz1-ethyl-Bz2-methylbenzanthrone.Info
- Publication number
- CH128117A CH128117A CH128117DA CH128117A CH 128117 A CH128117 A CH 128117A CH 128117D A CH128117D A CH 128117DA CH 128117 A CH128117 A CH 128117A
- Authority
- CH
- Switzerland
- Prior art keywords
- ethyl
- methylbenzanthrone
- preparation
- bzl
- oxymethylene
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von Bzl-Äthyl-Bz2-methylbenzanthron. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung des Bzl- Äthyl-Bzl-methylbenzanthrons, dadurch ge kennzeichnet, dass man Anthron und. (Oxy- methylen-äthyl)-äthylketonnatrium der fol genden Formel:
EMI0001.0007
unter Zusatz eines sauren Kondensations mittels kondensiert.
<I>Beispiel:</I> 25 Gewichtsteile (Oxymethylen-äthyl)- äthylketonnatrium werden in 80 Gewichts teilen Eisessig gelöst und diese Lösung zu einer solchen von 19 Gewichtsteilen Anthron in 200 Gewichtsteilen Schwefelsäure von 62 B6 bei gewöhnlicher Temperatur zuge- setzt. Nach kurzem Erwärmen auf dem Wasserbad hat das Reaktionsgemisch eine rein rote Farbe angenommen. Es wird auf Wasser gegossen und das abgeschiedene Benzanthronderivat in der üblichen Weise isoliert.
Das erhaltene Bzl-Äthyl-Bz2-me- thylbenzanthron kristallisiert aus Sprit in langen gelben Nadeln vom Schmelzpunkt 1420.
Process for the preparation of Bzl-ethyl-Bz2-methylbenzanthrone. The present invention relates to a method for the preparation of Bzl-ethyl-Bzl-methylbenzanthrone, characterized in that one anthrone and. (Oxymethylene-ethyl) -ethylketone sodium of the following formula:
EMI0001.0007
condensed with the addition of an acidic condensation means.
<I> Example: </I> 25 parts by weight of (oxymethylene-ethyl) ethyl ketone sodium are dissolved in 80 parts by weight of glacial acetic acid and this solution is added to one of 19 parts by weight of anthrone in 200 parts by weight of sulfuric acid of 62 B6 at ordinary temperature. After briefly warming up on the water bath, the reaction mixture has turned a pure red color. It is poured into water and the separated benzanthrone derivative isolated in the usual way.
The Bzl-ethyl-Bz2-methylbenzanthrone obtained crystallizes from fuel in long yellow needles with a melting point of 1420.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128117X | 1926-04-03 | ||
CH127266T | 1927-04-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128117A true CH128117A (en) | 1928-10-01 |
Family
ID=25710833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128117D CH128117A (en) | 1926-04-03 | 1927-04-02 | Process for the preparation of Bz1-ethyl-Bz2-methylbenzanthrone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128117A (en) |
-
1927
- 1927-04-02 CH CH128117D patent/CH128117A/en unknown
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