CH128113A - Process for the preparation of the Bz1-methylbenzanthrone. - Google Patents
Process for the preparation of the Bz1-methylbenzanthrone.Info
- Publication number
- CH128113A CH128113A CH128113DA CH128113A CH 128113 A CH128113 A CH 128113A CH 128113D A CH128113D A CH 128113DA CH 128113 A CH128113 A CH 128113A
- Authority
- CH
- Switzerland
- Prior art keywords
- methylbenzanthrone
- preparation
- bzl
- acetone
- anthrone
- Prior art date
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Darstellung des Bz1-illethylbenzanthrons. Gegenstand der vorliegenden. Erfindung ist ein Verfahren zur Darstellung des Bzl- Methylbenzanthrons, dadurch gekennzeich net, dass man Anthron und Oxymethylen- acetonnatrium von der folgenden Formel:
EMI0001.0010
unter Zusatz eines sauren Kondensations mittels kondensiert.
<I>Beispiel:</I> 13 Gewichtsteile Oxymethylenaceton- natrium [Ber. 21, 2144 u. Ber. 22, 3274] wer den in 40 Gewichtsteilen Eisessig gelöst und diese Lösung zu einer solchen von 19 Ge wichtsteilen Anthron in 100 Gewichtsteilen Schwefelsäure von 62 B6 gegeben. Der Re aktionsverlauf ist an der Farbe der Lösung, welche über grün-, blau- nach karminrot um- schlägt, deutlich zu verfolgen.
Das aus der karminroten Lösung, mit Wasser abgeschie dene Bzl-Methylbenzanthron ist identisch mit dem nach dem Hauptpatent Nr. 127266 erhaltenen. Die Benzanthronbildung ist in diesem Falle umso überraschender, als die grosse Neigung des Oxymethylenacetons zur Selbstkondensation unter Bildung von Tri- acetylbenzol bekannt ist.
Process for the preparation of the Bz1-illethylbenzanthrone. Subject of the present. Invention is a process for the preparation of Bzl methylbenzanthrone, characterized in that one anthrone and oxymethylene acetone sodium of the following formula:
EMI0001.0010
condensed with the addition of an acidic condensation means.
<I> Example: </I> 13 parts by weight of oxymethylene acetone sodium [Ber. 21, 2144 and Ber. 22, 3274] who dissolved the in 40 parts by weight of glacial acetic acid and this solution was added to one of 19 parts by weight of anthrone in 100 parts by weight of sulfuric acid of 62 B6. The course of the reaction can be clearly followed by the color of the solution, which changes from green to blue to carmine red.
The Bzl-methylbenzanthrone from the crimson solution with water is identical to that obtained according to the main patent no. 127266. The formation of benzanthrone is all the more surprising in this case as the great tendency of oxymethylene acetone to self-condense with the formation of triacetylbenzene is known.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128113X | 1926-04-03 | ||
CH127266T | 1927-04-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128113A true CH128113A (en) | 1928-10-01 |
Family
ID=25710829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128113D CH128113A (en) | 1926-04-03 | 1927-04-02 | Process for the preparation of the Bz1-methylbenzanthrone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128113A (en) |
-
1927
- 1927-04-02 CH CH128113D patent/CH128113A/en unknown
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