CH125130A - Process for the preparation of a basic derivative of cyanamide. - Google Patents
Process for the preparation of a basic derivative of cyanamide.Info
- Publication number
- CH125130A CH125130A CH125130DA CH125130A CH 125130 A CH125130 A CH 125130A CH 125130D A CH125130D A CH 125130DA CH 125130 A CH125130 A CH 125130A
- Authority
- CH
- Switzerland
- Prior art keywords
- cyanamide
- preparation
- basic derivative
- diethylamine
- reaction
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines basischen Derivates des Cyanamids. Es wurde gefunden, dass man zu dem im Hauptpatent beschriebenen Bisdiäthyl- aminoäthyl-cy ana.mid auch gelangen kann, wenn man Halogenätliyldiäthylamin auf Metallsalze des Cyanamids einwirken lässt.
Beispiel: 43 Gewichtsteile Cyanamidnatrium wer den in wässeriger Lösung mit<B>136</B> Gewichts teilen Chloräthyldiäthylamin unter gelinder Erwärmung verrührt. Die entstandene Base wird in Äther aufgenommen und in üblicher 'N#@reise isoliert. Sie besitzt die im Haupt patent beschriebenen Eigenschaften.
Man kann auch in Gegenwart anderer Lösungsmittel, wie zum Beispiel Alkohol, arbeiten. An Stelle des l@Tatriumsalzes des Cyanamids lassen sich auch beliebige andere Salze, wie zum Beispiel das Kalk- oder das Silbersalz, verwenden.
Ebenso lässt sich das Chloräthyldiäthy lamin durch andere Ilalo- enä.thyldiäthylamine ersetzen, oder diese können erst im Reaktionsgemisch aus Chlor- :litliyIdiäthylamin, zum Beispiel durch Zusatz kleinerer oder grösserer Mengen Brom- oder Todalkali, intermediär erzeugt werden. Statt der freien Halogenbasen verwendet man zweckmässig ihre Salze und setzt die Basen während der Reaktion, zum Beispiel durch Zusatz von Alkalikarbonat, in Freiheit.
Process for the preparation of a basic derivative of cyanamide. It has been found that the bisdiäthylaminoäthyl-cy ana.mid described in the main patent can also be obtained if haloethyl diethylamine is allowed to act on metal salts of cyanamide.
Example: 43 parts by weight of sodium cyanamide are stirred in an aqueous solution with 136 parts by weight of chloroethyl diethylamine under gentle heating. The resulting base is taken up in ether and isolated in the usual way. It has the properties described in the main patent.
You can also work in the presence of other solvents, such as alcohol. Any other salts, such as the lime or silver salt, can also be used instead of the sodium salt of cyanamide.
Likewise, the chloroethyl diethylamine can be replaced by other Ilaloenä.thyldiäthylamine, or these can only be produced as an intermediate in the reaction mixture of chloro-: lithium diethylamine, for example by adding smaller or larger amounts of bromine or dead alkali. Instead of the free halogen bases, it is expedient to use their salts and to set the bases free during the reaction, for example by adding alkali metal carbonate.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH122879T | 1926-06-20 | ||
CH125130T | 1926-06-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH125130A true CH125130A (en) | 1928-04-02 |
Family
ID=25709963
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH125130D CH125130A (en) | 1926-06-20 | 1926-06-20 | Process for the preparation of a basic derivative of cyanamide. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH125130A (en) |
-
1926
- 1926-06-20 CH CH125130D patent/CH125130A/en unknown
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