CH269072A - Process for the preparation of a basic ether of a p-substituted benzhydrol. - Google Patents
Process for the preparation of a basic ether of a p-substituted benzhydrol.Info
- Publication number
- CH269072A CH269072A CH269072DA CH269072A CH 269072 A CH269072 A CH 269072A CH 269072D A CH269072D A CH 269072DA CH 269072 A CH269072 A CH 269072A
- Authority
- CH
- Switzerland
- Prior art keywords
- ether
- preparation
- benzhydryl
- methyl
- benzhydrol
- Prior art date
Links
Landscapes
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines basischen Äthers eines p-substituierten Benzhydrole. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines basischen Äthers eines p-substituierten Benzhydrols. Das Verfahren ist dadurch gekennzeichnet, dass man einen p-Methyl-benzhydryl-(p-halogen- äthyl)-äther mit Dimethylamin umsetzt.
Die erhaltene neue Verbindung, der p Methyl-benzhydryl-dimethylaminoäthyl-äther, siedet unter 0,1 mm Druck bei 143 0. Sie soll therapeutische Verwendung finden.
<I>Beispiel:</I> 30,2 Teile * p-Methyl-benzhydryl-(@-chlor- äthyl)-äther, erhältlich durch Umsetzen von p-Methyl-benzhydryl-bromid und Äthylen- chlorhydrin, werden mit 10 Teilen Dimethyl- amin (100 /oig) in einem Einschlussrohr 4 Stunden auf 110 0 erhitzt. Darauf versetzt man das Reaktionsprodukt mit Wasser und säuert in der Kälte mit Essigsäure an.
Die durch Ausschütteln mit Äther von Neutral produkten befreite essigsaure Lösung wird kalt mit konz. Natronlauge alkalisch gestellt und ausgeäthert. Durch Eindampfen wird der p - Methyl - benzhydryl - dimethylaminoäthyl - äther vom Siedepunkt 1431 unter 0,1 mm Druck erhalten.
Process for the preparation of a basic ether of a p-substituted benzhydrol. The subject of the present patent is a process for the preparation of a basic ether of a p-substituted benzhydrol. The process is characterized in that a p-methylbenzhydryl (p-haloethyl) ether is reacted with dimethylamine.
The new compound obtained, the p methyl benzhydryl dimethylaminoethyl ether, boils at 143 0 under 0.1 mm pressure. It is said to find therapeutic use.
<I> Example: </I> 30.2 parts of * p-methyl-benzhydryl - (@ - chloro-ethyl) -ether, obtainable by reacting p-methyl-benzhydryl-bromide and ethylene-chlorohydrin, are mixed with 10 parts Dimethylamine (100%) heated to 110 ° for 4 hours in an inclusion tube. The reaction product is then mixed with water and acidified with acetic acid in the cold.
The acetic acid solution, freed from neutral products by shaking with ether, is cold with conc. Sodium hydroxide solution made alkaline and etherified. The p-methyl-benzhydryl-dimethylaminoethyl-ether of boiling point 1431 is obtained by evaporation under 0.1 mm pressure.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH264135T | 1947-09-12 | ||
CH269072T | 1947-09-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH269072A true CH269072A (en) | 1950-06-15 |
Family
ID=25730723
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH269072D CH269072A (en) | 1947-09-12 | 1947-09-12 | Process for the preparation of a basic ether of a p-substituted benzhydrol. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH269072A (en) |
-
1947
- 1947-09-12 CH CH269072D patent/CH269072A/en unknown
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