CH147051A - Process for the preparation of a derivative of 3.4.8.9-dibenzpyrene-5.10-quinone. - Google Patents
Process for the preparation of a derivative of 3.4.8.9-dibenzpyrene-5.10-quinone.Info
- Publication number
- CH147051A CH147051A CH147051DA CH147051A CH 147051 A CH147051 A CH 147051A CH 147051D A CH147051D A CH 147051DA CH 147051 A CH147051 A CH 147051A
- Authority
- CH
- Switzerland
- Prior art keywords
- quinone
- dibenzpyrene
- derivative
- preparation
- mol
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Derivates des 3.4.8.9-Dibenzpyren-6.10-chinons. Im Hauptpatent ist ein Verfahren zur Darstellung eines Derivates des 3.4.8.9- Dibenzpyrenchinons beschrieben, bei dem 3.4.8.9-Dibenzpyren-5.10-chinon in saurem Medium in Gegenwart von Katalysatoren mit mindestens 1 Mol eines chlorierend wirken den Mittels behandelt wird.
Es wurde nun gefunden, dass man ein Deri vat des 3.4.8.9-Dibenzpyren-5 . 10-chinons von ähnlichen Eigenschaften erhalten kann, wenn man 3.4. 8.9-Dibenzpyren-5.10-chinon in saurem Mediumin Gegenwart von Kataly satoren finit mindestens l/2 Mol eines bromfie- rend und mindestens 1/2 Mol eines chlorierend wirkenden Mittels behandelt.
Das erhaltene Reaktionsprodukt ist der Analyse nach ein Monobrommono-chlor- 3. 4. 8 . 9-dibenzpyi#en-5 .10-chinon, das sich in konzentrierter Schwefelsäure mit violetter Farbe löst und aus blauroter Küpe gelb orange Färbungen von sehr guter Echtheit liefert. Beispiel: 33,2 Teile 3.4.8.9-Dibenzpyreri-5.10- chinon werden in 300 Teilen Chlorsulfon- säure gelöst.
Man gibt ein Teil Jod hinzu, leitet bei<B>600</B> C so lange Chlor ein, bis die Gewichtszunahme einem 1/2 Mol Chlor ent spricht, fügt 9 Teile Brom bei<B>65-700</B> (l/' zu, rührt und arbeitet, sobald alles Brom aufgenommen ist, in der üblichen Weise auf.
Process for the preparation of a derivative of 3.4.8.9-dibenzpyrene-6.10-quinone. The main patent describes a process for the preparation of a derivative of 3.4.8.9-dibenzpyrenquinone, in which 3.4.8.9-dibenzpyren-5.10-quinone is treated in an acidic medium in the presence of catalysts with at least 1 mol of a chlorinating agent.
It has now been found that a derivative of 3.4.8.9-dibenzpyrene-5. 10-quinones of similar properties can be obtained if one 3.4. 8.9-dibenzpyrene-5.10-quinone in an acid medium in the presence of catalysts finitely treated at least 1/2 mol of a brominating agent and at least 1/2 mol of a chlorinating agent.
The reaction product obtained is, according to analysis, a monobromo mono-chloro-3. 4. 8. 9-dibenzpyi # en-5 .10-quinone, which dissolves in concentrated sulfuric acid with a violet color and, from a blue-red vat, gives yellow-orange colorations of very good fastness. Example: 33.2 parts of 3.4.8.9-dibenzpyreri-5.10-quinone are dissolved in 300 parts of chlorosulfonic acid.
One part iodine is added, chlorine is introduced at <B> 600 </B> C until the increase in weight corresponds to 1/2 mole of chlorine, and 9 parts bromine are added at <B> 65-700 </B> (1 / 'close, stir and work up as usual as soon as all the bromine has been taken up.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE147051X | 1928-06-30 | ||
CH143710T | 1929-06-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH147051A true CH147051A (en) | 1931-05-15 |
Family
ID=25714335
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH147051D CH147051A (en) | 1928-06-30 | 1929-06-18 | Process for the preparation of a derivative of 3.4.8.9-dibenzpyrene-5.10-quinone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH147051A (en) |
-
1929
- 1929-06-18 CH CH147051D patent/CH147051A/en unknown
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