CH204435A - Process for the preparation of 4,4'-tetrabutyl-diaminobenzophenone. - Google Patents
Process for the preparation of 4,4'-tetrabutyl-diaminobenzophenone.Info
- Publication number
- CH204435A CH204435A CH204435DA CH204435A CH 204435 A CH204435 A CH 204435A CH 204435D A CH204435D A CH 204435DA CH 204435 A CH204435 A CH 204435A
- Authority
- CH
- Switzerland
- Prior art keywords
- tetrabutyl
- preparation
- acid
- diaminobenzophenone
- phenylhydrazine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/22—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung von 4.4'-Tetrabutyl-diaminobenzophenon. Nach dem im Hauptpatent beschriebenen Verfahren wird 4.4'-Tetramethyldiamino- benzophenon in der Weise hergestellt, dass man 4. 4'-Tetramethyldiaminobenzhydrol mit Phenylhydrazin in Gegenwart einer geringen Menge Säure umsetzt, das erhaltene Konden sationsprodukt oxydiert und das Oxydations produkt mit Säure spaltet.
Gegenstand des vorliegenden Patentes ist nun ein Verfahren zur Herstellung von 4. 4' Tetrabutyl - diamino - benzophenon, welches dadurch gekennzeichnet ist, dass man das 4. 4'-Tetrabutyl-diaminobenzhydrol mit Phe- nylhydrazin in Gegenwart einer geringen Menge Säure umsetzt, das erhaltene Konden sationsprodukt oxydiert und das Oxydations produkt mit Säure spaltet.
<I>Beispiel:</I> 65 Gewichtsteile 4 . 4' - Tetrabutyl - di- aminobenzhydrpl werden mit 16,05 Gewichts- teilen Phenylhydrazin in alkoholischer Lö sung unter Zusatz von wenig Salzsäure kon densiert. Nach dem Verjagen des Alkohols setzt man 17 Gewichtsteile Wasser und 350 Volumenteile Aceton zu und oxydiert unter Rühren mit der berechneten Menge Kalium permanganat.
Nach Abfiltrieren des gebil deten Braunsteins treibt man das organische Lösungsmittel ab, kocht den in Wasser un löslichen Rückstand mit Salzsäure und fällt das gebildete Keton mit Natriumhydroxyd- lösung aus. Das so erhaltene 4.4'-Tetra- butyl-diamino-benzophenon bildet als Roh produkt einen dunkelgefärbten pulverigen Niederschlag, der für die Herstellung von Farbstoffen Verwendung finden soll.
Process for the preparation of 4,4'-tetrabutyl-diaminobenzophenone. According to the process described in the main patent, 4,4'-tetramethyldiamino benzophenone is prepared in such a way that 4, 4'-tetramethyldiaminobenzhydrol is reacted with phenylhydrazine in the presence of a small amount of acid, the resulting condensation product is oxidized and the oxidation product is cleaved with acid.
The present patent now relates to a process for the preparation of 4,4'-tetrabutyl - diamino - benzophenone, which is characterized in that the 4th 4'-tetrabutyl-diaminobenzhydrol is reacted with phenylhydrazine in the presence of a small amount of acid, which condensation product obtained is oxidized and the oxidation product cleaves with acid.
<I> Example: </I> 65 parts by weight 4. 4 '- Tetrabutyl - diminobenzhydrpl are condensed with 16.05 parts by weight of phenylhydrazine in alcoholic solution with the addition of a little hydrochloric acid. After the alcohol has been driven off, 17 parts by weight of water and 350 parts by volume of acetone are added and the mixture is oxidized with the calculated amount of potassium permanganate while stirring.
After filtering off the brownstone formed, the organic solvent is driven off, the residue, which is insoluble in water, is boiled with hydrochloric acid and the ketone formed is precipitated with sodium hydroxide solution. The 4,4'-tetra-butyl-diamino-benzophenone obtained in this way forms a dark-colored powdery precipitate as a crude product, which is said to be used for the production of dyes.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE204435X | 1936-08-26 | ||
CH198707T | 1937-05-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH204435A true CH204435A (en) | 1939-04-30 |
Family
ID=25723116
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH204435D CH204435A (en) | 1936-08-26 | 1937-05-24 | Process for the preparation of 4,4'-tetrabutyl-diaminobenzophenone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH204435A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3691157A (en) * | 1970-08-12 | 1972-09-12 | Rodney Ian Fryer | Preparation of 7-substituted-1-(2-diethylaminoethyl)-5-(2-halophenyl)-1,3-dihydro-2h-1,4-benzodiazepin-2-ones |
-
1937
- 1937-05-24 CH CH204435D patent/CH204435A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3691157A (en) * | 1970-08-12 | 1972-09-12 | Rodney Ian Fryer | Preparation of 7-substituted-1-(2-diethylaminoethyl)-5-(2-halophenyl)-1,3-dihydro-2h-1,4-benzodiazepin-2-ones |
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