CH147685A - Process for the preparation of an aminodiphenylamine derivative. - Google Patents
Process for the preparation of an aminodiphenylamine derivative.Info
- Publication number
- CH147685A CH147685A CH147685DA CH147685A CH 147685 A CH147685 A CH 147685A CH 147685D A CH147685D A CH 147685DA CH 147685 A CH147685 A CH 147685A
- Authority
- CH
- Switzerland
- Prior art keywords
- derivative
- aminodiphenylamine
- preparation
- parts
- chlorodiphenylamine
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Aminodiplienylaminderivates. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Aminodi- phenylaminderivates, dadurch gekennzeichnet, dass man p-Chlornitrosobenzol mit Nitroso- benzol kondensiert und das Kondensations produkt mit einem Reduktionsmittel behandelt.
Das erhaltene 4-Amino-4'-chlordiphenyl- amin schmilzt nach Umkristallisieren bei 70 bis 71 . Es soll als Zwischenprodukt zur Herstellung von Farbstoffen verwendet werden. Das 4-Amino-4'-chlordiphenylamin ist von Jacobsen, Annalen 303, Seite 312 und 314 beschrieben.
Beispiel: 70;5 Teile p-Chlorniti-osobenzol und 53,5 Teile Nitrosobenzol werden in 400 Teilen Eisessig gelöst und in 1500 Teile Schwefel säure von 66 B6 bei -i-- 5 innerhälb 2 Stun den eintropfen gelassen. Die klare Lösung wird in Eiswasser gegossen, das ausgeschie dene Kondensationsprodukt abgesaugt und säurefrei gewaschen; es hat- den Schmelz punkt 143 .
Die Lösung desselben in 3000 Teilen Wasser und 65 Teilen Natronlauge von 38 Bö wird bei 60 mit einer Lösung von 175 Teilen wasserfreiem Schwefelnatrium in der nötigen Menge Wasser versetzt und auf 80 erwärmt. Nach ungefähr einer halben Stunde ist unter Entfärbung der Flüssigkeit die Reduktion eingetreten und das gebildete Aminodiphenylaminderivat aus geschieden. Nach dem Erkalten wird das selbe abfiltriert.
Process for the preparation of an aminodiplienylamine derivative. The present patent relates to a process for the preparation of an aminodiphenylamine derivative, characterized in that p-chloronitrosobenzene is condensed with nitrosobenzene and the condensation product is treated with a reducing agent.
The 4-amino-4'-chlorodiphenylamine obtained melts at 70 to 71 after recrystallization. It is intended to be used as an intermediate in the manufacture of dyes. The 4-amino-4'-chlorodiphenylamine is described by Jacobsen, Annalen 303, pages 312 and 314.
Example: 70; 5 parts of p-chloroniti-osobenzene and 53.5 parts of nitrosobenzene are dissolved in 400 parts of glacial acetic acid and allowed to drip into 1500 parts of sulfuric acid of 66 B6 at -i-- 5 within 2 hours. The clear solution is poured into ice water, the condensation product excreted is suctioned off and washed free of acid; it has a melting point of 143.
A solution of 175 parts of anhydrous sodium sulphide in the necessary amount of water is added at 60 to the solution of this in 3000 parts of water and 65 parts of 38 boilers of sodium hydroxide solution and heated to 80. After about half an hour, the reduction has taken place with discoloration of the liquid and the aminodiphenylamine derivative formed has separated out. After cooling, the same is filtered off.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE147685X | 1929-02-15 | ||
CH145992T | 1929-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH147685A true CH147685A (en) | 1931-06-15 |
Family
ID=25714776
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH147685D CH147685A (en) | 1929-02-15 | 1929-09-20 | Process for the preparation of an aminodiphenylamine derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH147685A (en) |
-
1929
- 1929-09-20 CH CH147685D patent/CH147685A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH147685A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
CH147686A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
CH147681A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
DE436524C (en) | Process for the preparation of 2-oxynaphthalene-6-carboxylic acid | |
CH147680A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
CH147684A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
DE511526C (en) | Process for the preparation of 4-aminodiphenylamine derivatives | |
CH104252A (en) | Process for the preparation of di-carbethoxy-di-phenolisatin. | |
CH176225A (en) | Process for the preparation of 2-chloro-2'-aminoazobenzene. | |
AT107857B (en) | Process for the preparation of quinine salts of oxyphenylarsinic acids. | |
CH147683A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
CH127927A (en) | Process for the production of a new anthraquinone derivative. | |
CH147682A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
CH175892A (en) | Process for the preparation of 4-methyl-2-amino-2'.4'-dichloroazobenzene. | |
CH167377A (en) | Process for the preparation of 1-acetylamino-2,4-dimethylbenzene-5-sulfonic acid chloride. | |
CH147687A (en) | Process for the preparation of an aminodiphenylamine derivative. | |
CH194997A (en) | Process for the preparation of N- (γ-diethylaminopropyl) -5-amino-m-phenanthroline. | |
CH170688A (en) | Process for the preparation of 1,4-diaminoanthraquinone-2,3-disulfonic acid. | |
CH193341A (en) | Process for the preparation of 3-nitro-4-dodecylaniline. | |
CH106124A (en) | Process for the preparation of 4-chloro-1,2-thionaphthisatin. | |
CH106133A (en) | Process for the preparation of 2,3-thionaphthisatin. | |
CH135382A (en) | Process for the preparation of a monohalogen naphthostyril derivative. | |
CH145032A (en) | Process for the preparation of 6-chloro-7-methylisatin. | |
CH151867A (en) | Process for the preparation of 6-p-tolylamino-2-naphthol. | |
CH182585A (en) | Process for the preparation of a heterocyclic amino compound. |