CH85679A - Process for the preparation of a therapeutically valuable derivative of p-aminophenol. - Google Patents
Process for the preparation of a therapeutically valuable derivative of p-aminophenol.Info
- Publication number
- CH85679A CH85679A CH85679DA CH85679A CH 85679 A CH85679 A CH 85679A CH 85679D A CH85679D A CH 85679DA CH 85679 A CH85679 A CH 85679A
- Authority
- CH
- Switzerland
- Prior art keywords
- aminophenol
- preparation
- therapeutically valuable
- derivative
- valuable derivative
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
Description
Verfahren zur Darstellung eine' therapeutisch wertvollen Derivates des p-Amino- phenols. erstarrt kristallinisch und wird aus Wasser uinkristallisiei-t. Er besitzt die in der Haupt: auineldung beschriebenen Eigenschaften.
Statt Allylbromid können andere Allylie- rungsmittel, zum Beispiel andere Allylhalo- genide, verwendet werden. Es wurde gefunden, dass man zu dem in der Patentschrift 1\'r. 78044 beschriebenen p-Lactylaminopheiiolally läthei, auch gelangen kann, wenn man Lactyl-p-aminophenol mit allylierenden Mitteln behandelt.
Beispiel 179 Teile Lactyl-p-aminophenol werden in 300 Teilen Alkohol gelöst und mit 121 Teilen Allylbromid versetzt. Man fügt hierauf eine Lösung von 56 Teilen Ätzkali in 200 Teilen Alkohol hinzu und kocht während 48 Stunden am Rückflusskühler. Man filtriert hierauf vom ausgeschiedenen Bromkali ab, destilliert den grössten Teil des Alkohols ab und versetzt den Rückstand mit Wasser. Der entstandene Lactyl-p-aminopheriolallyläther
Process for the preparation of a 'therapeutically valuable derivative of p-aminophenol. solidifies in a crystalline manner and becomes uncrystallized from water. It has the properties described in the main message.
Instead of allyl bromide, other allylating agents, for example other allyl halides, can be used. It has been found that to the one described in patent specification 1 \ 'r. 78044 described p-Lactylaminopheiiolally läthei, can also get if you treat lactyl-p-aminophenol with allylating agents.
Example 179 parts of lactyl-p-aminophenol are dissolved in 300 parts of alcohol, and 121 parts of allyl bromide are added. A solution of 56 parts of caustic potash in 200 parts of alcohol is then added and the mixture is refluxed for 48 hours. The precipitated potassium bromide is then filtered off, most of the alcohol is distilled off and water is added to the residue. The resulting lactyl-p-aminopheriol allyl ether
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH85679T | 1917-11-17 | ||
CH76619T | 1917-11-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH85679A true CH85679A (en) | 1920-07-01 |
Family
ID=25701876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH85679D CH85679A (en) | 1917-11-17 | 1917-11-17 | Process for the preparation of a therapeutically valuable derivative of p-aminophenol. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH85679A (en) |
-
1917
- 1917-11-17 CH CH85679D patent/CH85679A/en unknown
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