CH147682A - Process for the preparation of an aminodiphenylamine derivative. - Google Patents
Process for the preparation of an aminodiphenylamine derivative.Info
- Publication number
- CH147682A CH147682A CH147682DA CH147682A CH 147682 A CH147682 A CH 147682A CH 147682D A CH147682D A CH 147682DA CH 147682 A CH147682 A CH 147682A
- Authority
- CH
- Switzerland
- Prior art keywords
- aminodiphenylamine
- derivative
- preparation
- nitrosotoluene
- production
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Aminodiphenylaminderivates. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Aminodi- phenylaminderivates, dadurch gekennzeichnet, dass man p-Nitrosotoluol mit o-Nitrosotoluol kondensiert und das Kondensationsprodukt mit einem Reduktionsmittel behandelt.
Durch Kristallisation des salzsauren Salzes gereinigt, hat das erhaltene, bisher nicht bekannte 4'.<B>3 -</B> Dimethyl-4-amiiiodiphenylamin den Schmelzpunkt<B>73-74 0.</B> Es soll als Zwischenprodukt zur Herstellung von Farb stoffen verwendet werden.
<I>Beispiel:</I> Je<B>60</B> Teile p-Nitrosotoluol und o-Nitroso- toluol werden zusammen geschmolzen und noch warm in<B>1000</B> Teile Schwefelsäure von <B>60 1</B> B6 bei<B>8-10 1</B> in einer Stunde eintropfen gelassen. Die klare Lösung wird in Eiswasser ausgegossen, wobei das Kondensationsprodukt in bräunlichen Flocken ausfällt.
Es wird ab gesaugt, gewaschen (Schmelzpunkt des gelb braunen Körpers nach Umlösen mit Natron lauge und Fällen mit Salzsäure<B>157-158 0)</B> in etwa<B>5000</B> Volumteilen verdünnter Natron lauge gelöst und vom geringen braunen Rück stand abfiltriert. Die klare, tiefrote Lösung wird mit einer Lösung von<B>180</B> Teilen ge schmolzenem Schwefelnatrium in Wasser versetzt und langsam auf<B>80 0</B> erwärmt, wobei das Reduktionsprodukt ölig ausfällt, aber beim Erkalten schnell erstarrt.
Process for the preparation of an aminodiphenylamine derivative. The present patent relates to a process for the preparation of an aminodiphenylamine derivative, characterized in that p-nitrosotoluene is condensed with o-nitrosotoluene and the condensation product is treated with a reducing agent.
Purified by crystallization of the hydrochloric acid salt, the previously unknown 4 '. <B> 3 - </B> dimethyl-4-amiiodiphenylamine obtained has the melting point <B> 73-74 0. </B> It is said to be an intermediate product for Manufacture of dyes are used.
<I> Example: </I> <B> 60 </B> parts each of p-nitrosotoluene and o-nitrosotoluene are melted together while still warm into <B> 1000 </B> parts of sulfuric acid of <B> 60 1 </B> B6 at <B> 8-10 1 </B> allowed to drip in in one hour. The clear solution is poured into ice water, the condensation product precipitating in brownish flakes.
It is sucked off, washed (melting point of the yellow-brown body after dissolving with caustic soda and precipitating with hydrochloric acid <B> 157-158 0) </B> in about <B> 5000 </B> parts by volume of dilute caustic soda and dosed small brown residue was filtered off. The clear, deep red solution is mixed with a solution of <B> 180 </B> parts of molten sodium sulphide in water and slowly heated to <B> 80 0 </B>, the reduction product precipitating out as an oily product, but solidifying quickly on cooling .
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE147682X | 1928-10-09 | ||
CH145992T | 1929-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH147682A true CH147682A (en) | 1931-06-15 |
Family
ID=25714773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH147682D CH147682A (en) | 1928-10-09 | 1929-09-20 | Process for the preparation of an aminodiphenylamine derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH147682A (en) |
-
1929
- 1929-09-20 CH CH147682D patent/CH147682A/en unknown
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