AT48332B - Process for the preparation of optically active o-dioxyphenylalkamines. - Google Patents
Process for the preparation of optically active o-dioxyphenylalkamines.Info
- Publication number
- AT48332B AT48332B AT48332DA AT48332B AT 48332 B AT48332 B AT 48332B AT 48332D A AT48332D A AT 48332DA AT 48332 B AT48332 B AT 48332B
- Authority
- AT
- Austria
- Prior art keywords
- dioxyphenylalkamines
- optically active
- preparation
- racemic
- desc
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung optisch aktiver o-Dioxyphenylalkamine.
Es wurde gefunden. dass die synthetischen, optisch inaktiven, razemischen o-Dioxyphenylalliamine durch ihrer d-oder -weinsauren Salze in die optisch aktiven Komponenten gespalten werden Rönnen, und dass man so z. H. zu dem l-o-Dioxyphenyläthanolmethylamin gelangen kann, welches identisch ist mit der für therapeutische Zwecke wichtigen Neben-
EMI1.1
halten. Es schmilzt dann bei 1490 C. Es ist identisch mit dem d-weinsauren Salz der Neben- nierenbase. Die aus demselben durch Alkalilange abgeschiedene Base zeigt deren Schmelz-
EMI1.2
wird die d-hase in Form des schwer löslichen l-Tartrats abgetrennt.
In gleicher Weiso kann die Spaltung anderer razemischen o-Dioxyphenylalkamine mit Hilfe von d-Weinsüure ausgeführt werden.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for the preparation of optically active o-dioxyphenylalkamines.
It was found. that the synthetic, optically inactive, racemic o-dioxyphenylalliamines can be split into the optically active components by their d- or -tartaric acid salts, and that, for example, H. to the l-o-Dioxyphenyläthanolmethylamin, which is identical to the important for therapeutic purposes secondary
EMI1.1
hold. It then melts at 1490 C. It is identical to the d-tartaric acid salt of the adrenal base. The base separated from it by alkali length shows its melting point
EMI1.2
the d-hare is separated in the form of the poorly soluble l-tartrate.
In the same way, the cleavage of other racemic o-dioxyphenylalkamines can be carried out with the aid of d-tartaric acid.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE48332X | 1908-07-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT48332B true AT48332B (en) | 1911-06-10 |
Family
ID=5625945
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT48332D AT48332B (en) | 1908-07-31 | 1909-03-10 | Process for the preparation of optically active o-dioxyphenylalkamines. |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT48332B (en) |
-
1909
- 1909-03-10 AT AT48332D patent/AT48332B/en active
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