CH247919A - Process for the preparation of a new amide derivative. - Google Patents
Process for the preparation of a new amide derivative.Info
- Publication number
- CH247919A CH247919A CH247919DA CH247919A CH 247919 A CH247919 A CH 247919A CH 247919D A CH247919D A CH 247919DA CH 247919 A CH247919 A CH 247919A
- Authority
- CH
- Switzerland
- Prior art keywords
- amide derivative
- tri
- preparation
- mol
- acid amide
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 237621. Verfahren zur Herstellung eines neuen Amidderivats. Es wurde gefunden, dass man zu einem neuen Amidderivat gelangt, wenn man etwa 1 Mol technisches 0,lsäureamid, etwa 1 Mol Formaldehyd und etwa 1 Mol Triäthanolamin- tri-(oxyäthyläther) aufeinander einwirken lässt.
Die Umsetzung wird vorteilhaft in der Wärme, z. B. bei 100-140 , vorgenommen, zweckmässig unter Zusatz von die Reaktion beschleunigenden Stoffen, beispielsweise in Gegenwart von Alkalicarbonaten, wie Na- triumcarbonat.
Als Stoffe, die die Reaktion befördern, können auch konzentrierte, wasserlösliche, organische Säuren, wie Eisessig oder Ameisen säure, dienen. Es ist zweckmässig, das Amid erst mit Formaldehyd in bekannter Weise zum N-Methylo.la-midumzusetzen und anschlie ssend Triäthanolamin-tri-(oxyäthyläther) auf (las N-1VIethylolamid einwirken zu lassen.
Das neue Amidderivat bildet eine dick flüssige Masse, die bei Raumtemperatur zu einer annähernd klaren Lösung aufgenom men wird. Es kann als Textilhilfsstoff, z. B. als Weichmachungsmittel für Viskosekunst- seide, angewendet werden.
Beispiel: Man vermischt 10 Teile des in bekannter Weise aus technischem Ölsäureamid und Formaldehyd erhaltenen 0lsäure-N-methylol- amids mit 10 Teilen Triäthanolamin-trioxy- äthyläther und 10 Teilen wasserfreiem Na triumearbonat und erhitzt im Stickstoffstrom während etwa 11/ Stunden in einem Bad von 115-120 .
Man verrührt anschliessend mit 22 4 Teilen Wasser, erwärmt auf 40-50 und trocknet den ungelöst bleibenden Anteil. Man erhält 18 Teile einer dickflüssigen Masse, die bei Raumtemperatur von Wasser zu einer an nähernd klaren Lösung aufgenommen wird.
Additional patent to main patent no. 237621. Process for the preparation of a new amide derivative. It has been found that a new amide derivative is obtained if about 1 mole of technical grade 0, oleic acid amide, about 1 mole of formaldehyde and about 1 mole of triethanolamine tri- (oxyethyl ether) are allowed to act on one another.
The reaction is advantageous in the heat, e.g. B. at 100-140, made, expediently with the addition of substances which accelerate the reaction, for example in the presence of alkali carbonates, such as sodium carbonate.
Concentrated, water-soluble, organic acids such as glacial acetic acid or formic acid can also serve as substances that promote the reaction. It is advisable to first react the amide with formaldehyde in a known manner to form N-methylola-mid and then to allow triethanolamine tri (oxyethyl ether) to act on (read N-1V-ethylolamide.
The new amide derivative forms a thick, liquid mass that is absorbed into an almost clear solution at room temperature. It can be used as a textile auxiliary, e.g. B. can be used as a softener for viscose silk.
Example: Mix 10 parts of the obtained in a known manner from technical oleic acid amide and formaldehyde 0läur-N-methylolamide with 10 parts of triethanolamine trioxy ethyl ether and 10 parts of anhydrous sodium carbonate and heated in a stream of nitrogen for about 11 / hours in a bath of 115-120.
The mixture is then stirred with 22 4 parts of water, heated to 40-50 and the portion remaining undissolved is dried. 18 parts of a viscous mass are obtained, which is taken up by water at room temperature to form an almost clear solution.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH247919T | 1943-04-22 | ||
CH237621T | 1943-04-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH247919A true CH247919A (en) | 1947-03-31 |
Family
ID=25728272
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH247919D CH247919A (en) | 1943-04-22 | 1943-04-22 | Process for the preparation of a new amide derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH247919A (en) |
-
1943
- 1943-04-22 CH CH247919D patent/CH247919A/en unknown
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