CH245887A - Process for the preparation of an acylated, aliphatic aminocarboxamide. - Google Patents
Process for the preparation of an acylated, aliphatic aminocarboxamide.Info
- Publication number
- CH245887A CH245887A CH245887DA CH245887A CH 245887 A CH245887 A CH 245887A CH 245887D A CH245887D A CH 245887DA CH 245887 A CH245887 A CH 245887A
- Authority
- CH
- Switzerland
- Prior art keywords
- acylated
- preparation
- aliphatic
- aminocarboxamide
- acid dimethylamide
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines acylierten, aliphatischen Aminocarbonsäureamids. Gegenstand des vorliegenden Zusatzpaten tes ist ein Verfahren zur Darstellung eines acylierten, aliphatischen Aminocarbonsäure- amids. Das Verfahren ist dadurch gekenn zeichnet,
dass ein Halogen-ess.igsäuredime- thylamid mit Äthylamin umgesetzt und das Reaktionsprodukt mit einer das Radikal der Crotonsäure abgebenden Verbindung acyliert wird.
Das N-Crotonyl-äthylamino-essigsäure- dimethylamid der Formel
EMI0001.0017
bildet eine farblose Flüssigkeit vom Siede punkt 185 bis 186 unter 0,5 mm.
Die neue Verbindung soll als Lösungs vermittler Verwendung finden.
<I>Beispiel:</I> 24 Teile Ithylamino-essigsäuredimethyl- amid, Kp" 99 bis 102 (dargestellt aus Chlor- essigsäuredimethylamid durch Erhitzen mit Äthylamin), werden in 200 Teilen Äther gelöst und unter Rühren und Kühlen 10,4 Teile Crotonsäurechlorid zugetropft. Nach 2stündigem Rühren wird vom Äthylamino- essigsäuredimethylamid - Chlorhydrat abfil- triert und die ätherische Lösung mit ge sättigter Kalilauge .geschüttelt.
Nach dem Ab destillieren des Lösungsmittels wird das, Reak tionsprodukt im Hochvakuum rektifiziert. Die neue Verbindung siedet bei 185 bis 186 unter 0,5 mm und ist leicht löslich in Wasser und organischen Lösungsmitteln.
Process for the preparation of an acylated, aliphatic aminocarboxamide. The present additional patent is a process for the preparation of an acylated, aliphatic aminocarboxylic acid amide. The procedure is characterized by
that a halo-acetic acid dimethylamide is reacted with ethylamine and the reaction product is acylated with a compound that releases the crotonic acid radical.
The N-crotonyl-ethylamino-acetic acid dimethylamide of the formula
EMI0001.0017
forms a colorless liquid with a boiling point of 185 to 186 below 0.5 mm.
The new connection should be used as a solution mediator.
<I> Example: </I> 24 parts of ethylamino-acetic acid dimethyl amide, bp "99 to 102 (prepared from chloroacetic acid dimethyl amide by heating with ethylamine) are dissolved in 200 parts of ether and 10.4 parts of crotonic acid chloride are dissolved with stirring and cooling After stirring for 2 hours, the ethylaminoacetic acid dimethylamide chlorohydrate is filtered off and the ethereal solution is shaken with saturated potassium hydroxide solution.
After the solvent has been distilled off, the reaction product is rectified in a high vacuum. The new compound boils at 185 to 186 below 0.5 mm and is easily soluble in water and organic solvents.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH242836T | 1942-12-18 | ||
CH245887T | 1942-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH245887A true CH245887A (en) | 1946-11-30 |
Family
ID=25728734
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH245887D CH245887A (en) | 1942-12-18 | 1942-12-18 | Process for the preparation of an acylated, aliphatic aminocarboxamide. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH245887A (en) |
-
1942
- 1942-12-18 CH CH245887D patent/CH245887A/en unknown
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