CH131960A - Process for the preparation of 1-amino-3-dimethylamino-2-propanol. - Google Patents
Process for the preparation of 1-amino-3-dimethylamino-2-propanol.Info
- Publication number
- CH131960A CH131960A CH131960DA CH131960A CH 131960 A CH131960 A CH 131960A CH 131960D A CH131960D A CH 131960DA CH 131960 A CH131960 A CH 131960A
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- propanol
- dimethylamino
- preparation
- dimethylamine
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
Yerfahreu zur Darstellung von 1-Amino-3-dimethslamino-2-propanol. Es wurde gefunden, dass man das bisher nicht bekannte 1-Amino-3-dimethylamino-2- propanol gewinnen kann, wenn man auf 3-Halogen -2-oxypi-opylplitalimid Dimethyl- amin einwirken lässt und aus dem erhaltenen Produkt den Phtalsäurerest abspaltet.
Beispiel: 130 gr 3-Chlor-2-ogypropylpbtalimid wer- den mit 175 gr einer 30 %igen alkoholischen Dimethylaminlösung 4 Stunden lang in der Dampfbombe erhitzt.
Der Bombeninhalt wird darauf eingedampft, derzurückbleibende Syrup 4 Stunden mit 750 cm' 20%iger Salzsäure gekocht, die Lösung nach dem Erkalten von der Phtalsäure getrennt und im Vakuum bis zur Syrupdicke eingeengt. Der Syrup wird mit konzentrierter Natronlauge und darauf mit Pottasche bis zur Bildung eines dicken Breis versetzt, der wiederholt mit Benzol di- geriert wird.
Die Benzolauszüge werden nach dem Trocknen mit Kaliumkarbonat vom Ben- zol befreit und der Rückstand im Vakuum destilliert.
Die neue Base siedet unter 28 mm Druck bei 103 0. Sie bildet ein basisch riechendes, farbloses Öl und gibt ein festes, jedoch äusserst hygroskopisches Chlorhydrat.
Yerfahreu for the preparation of 1-amino-3-dimethslamino-2-propanol. It has been found that the previously unknown 1-amino-3-dimethylamino-2-propanol can be obtained if dimethylamine is allowed to act on 3-halo -2-oxypi-opylplitalimide and the phthalic acid residue is split off from the product obtained.
Example: 130 grams of 3-chloro-2-ogypropyl pbtalimide are heated in a steam bomb for 4 hours with 175 grams of a 30% alcoholic dimethylamine solution.
The contents of the bomb are then evaporated, the remaining syrup is boiled for 4 hours with 750 cm 'of 20% hydrochloric acid, the solution is separated from the phthalic acid after cooling and concentrated in vacuo to the syrup thickness. Concentrated sodium hydroxide solution and then potash are added to the syrup until a thick paste forms, which is repeatedly digested with benzene.
After drying with potassium carbonate, the benzene extracts are freed from benzene and the residue is distilled in vacuo.
The new base boils at 103 0 under 28 mm pressure. It forms a colorless oil with a basic odor and gives a solid, but extremely hygroscopic hydrochloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE131960X | 1926-08-13 | ||
CH130697T | 1927-08-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH131960A true CH131960A (en) | 1929-03-15 |
Family
ID=25711486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH131960D CH131960A (en) | 1926-08-13 | 1927-08-11 | Process for the preparation of 1-amino-3-dimethylamino-2-propanol. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH131960A (en) |
-
1927
- 1927-08-11 CH CH131960D patent/CH131960A/en unknown
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