CH122521A - Process for the preparation of an aralkylamine. - Google Patents
Process for the preparation of an aralkylamine.Info
- Publication number
- CH122521A CH122521A CH122521DA CH122521A CH 122521 A CH122521 A CH 122521A CH 122521D A CH122521D A CH 122521DA CH 122521 A CH122521 A CH 122521A
- Authority
- CH
- Switzerland
- Prior art keywords
- guaiacol
- preparation
- aralkylamine
- parts
- halomethylphthalimide
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Aralkylamins. Es wurde gefunden, dass man nach dem im Hauptpatent beschriebenen Verfahren 4-Oxy-3-methoxybenzylamin herstellen kann, wenn man an Stelle des dort verwendeten Benzols Guajakol verwendet.
<I>Beispiel:</I> 63 Teile Guajakol und 32 Teile co-Chlor- methylphtalimid werden ohne Anwendung eines Katalysators durch Erwärmen bis etwa auf 120 o C zu 4-Oxy-3-methoxybenzylphtal- imid vom Schmelzpunkt 154 o kondensiert, wobei, wie ersichtlich, das Guajakol, das gleichzeitig Lösungsmittel ist, im Überschuss vorhanden ist. 50 Teile der Verbindung wer den mit 50 Teilen Alkohol, 100 Teilen 35 o/oiger Natriumhydroxydlösung und 200 Teilen Wasser kalt 2 ,Stunden lang gerührt.
Dann wird mit verdünnter Salzsäure ange säuert und der Alkohol verjagt und etwa ausgeschiedenes Öl durch Wasserzusatz in Lösung gebracht. Bei der Aufarbeitung er hält man das 4-Oxy-3-methoxybenzylamin- chlorhydrat, durch Zusatz von Natriumhydro- xyd und Ausäthern die freie Base.
Das Verfahren lässt sich auch in Gegen wart eines Katalysators, z. B. Chlorzink, durchführen.
Das erhaltene, an sich bekannte Produkt soll als Zwischenprodukt bei der Darstellung technisch wichtige Stoffe, wie Riechstoffe und Heilmittel, Verwendung finden.
Process for the preparation of an aralkylamine. It has been found that 4-oxy-3-methoxybenzylamine can be prepared by the process described in the main patent if guaiacol is used instead of the benzene used there.
<I> Example: </I> 63 parts of guaiacol and 32 parts of co-chloromethylphthalimide are condensed without using a catalyst by heating to about 120 ° C. to give 4-oxy-3-methoxybenzylphthalimide with a melting point of 154 °, with As can be seen, the guaiacol, which is also a solvent, is present in excess. 50 parts of the compound who stirred the cold with 50 parts of alcohol, 100 parts of 35 o / o sodium hydroxide solution and 200 parts of water for 2 hours.
Then it is acidified with dilute hydrochloric acid and the alcohol is driven off and any oil that has separated out is brought into solution by adding water. During work-up, the 4-oxy-3-methoxybenzylamine chlorohydrate is obtained, and the free base is obtained by adding sodium hydroxide and ether.
The method can also be used in the presence of a catalyst, e.g. B. zinc chloride, perform.
The product obtained, known per se, is intended to be used as an intermediate product in the preparation of technically important substances such as fragrances and medicinal products.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE122521X | 1925-03-30 | ||
CH120519T | 1926-03-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH122521A true CH122521A (en) | 1927-09-16 |
Family
ID=25709456
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH122521D CH122521A (en) | 1925-03-30 | 1926-03-23 | Process for the preparation of an aralkylamine. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH122521A (en) |
-
1926
- 1926-03-23 CH CH122521D patent/CH122521A/en unknown
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