CH242605A - Process for the preparation of a new derivative of a ring-substituted aromatic oxy compound. - Google Patents
Process for the preparation of a new derivative of a ring-substituted aromatic oxy compound.Info
- Publication number
- CH242605A CH242605A CH242605DA CH242605A CH 242605 A CH242605 A CH 242605A CH 242605D A CH242605D A CH 242605DA CH 242605 A CH242605 A CH 242605A
- Authority
- CH
- Switzerland
- Prior art keywords
- ring
- substituted aromatic
- preparation
- oxy compound
- new derivative
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen -Derivats einer kernsubstituierten aromatischen Ogyverbindung. Es wurde gefunden, dass man zu ,einem neuen Derivat einer kernsubstituierten aro matischen Oxyverbindung gelangt, wenn man das Kondensationsprodukt aus Kokosfett- säure-N-methylolamid und Phenol mit Form aldehyd und Diäthanolamin kondensiert.
Die Kondensation wird zweckmässig in der Wärme, z. B. bei 60 bis 100 , ausgeführt. Das neue Erzeugnis bildet eine ziemlich zähe Masse, die nach dem Lösen in Eisessig beim Verdünnen mit Wasser eine annähernd klare, schäumende Lösung liefert. Es kann als Textilhilfsstoff Anwendung finden.
<I>Beispiel:</I> Man vermischt 31,8 Teile des Konden- sationsproduktes aus Kokosfettsäure-N-me- thylolamid und Phenol mit 11,6 Teilen Di- äthanolamin, lässt bei Raumtemperatur 9 Teile wässrige, 36,6 % ige Formaldehyd lösung innert etwa 1 Stunde hinzufliessen und erhitzt während etwa 3 Stunden auf 85 bis 90 .
Das mit Wasser gewaschene neue Erzeugnis bildet nach dem Trocknen eine ziemlich zähe Masse, die nach dem Lösen in Eisessig beim Verdünnen mit Wasser eine annähernd klare, schäumende Lösung liefert. Das neue Erzeugnis kann z. B. als Textil hilfsstoff Anwendung finden.
Zur Herstellung des als Ausgangs material dienenden Kondensationsproduktes kann man wie folgt verfahren: Man löst 72,6 Teile Kokosf ettsäure - N - methylolamid und 30;9 Teile Phenol in 200 Teilen Eisessig, fügt 72,6 Teile entwässertes Zinkchlorid hinzu und erwärmt während 24 Stunden auf 45 bis 50 . Das mit Wasser gewaschene, von gerin gen Mengen unverändertem Phenol durch Ab blasen mit Wasserdampf befreite Erzeugnis, eine weiche Masse, ist nach dem Lösen in alkoholischer galiumhydroxydlösung mit Wasser klar verdünnbar.
Process for the preparation of a new derivative of a ring-substituted aromatic ogy compound. It has been found that a new derivative of a ring-substituted aromatic oxy compound is obtained if the condensation product of coconut fatty acid-N-methylolamide and phenol is condensed with formaldehyde and diethanolamine.
The condensation is expedient in the heat, for. B. at 60 to 100 executed. The new product forms a rather viscous mass which, when dissolved in glacial acetic acid, when diluted with water produces an almost clear, foaming solution. It can be used as a textile auxiliary.
<I> Example: </I> 31.8 parts of the condensation product of coconut fatty acid N-methylolamide and phenol are mixed with 11.6 parts of diethanolamine, and 9 parts of 36.6% aqueous solution are left at room temperature Add formaldehyde solution within about 1 hour and heat to 85 to 90 for about 3 hours.
The new product, washed with water, forms a rather viscous mass after drying, which, when dissolved in glacial acetic acid, produces an almost clear, foaming solution when diluted with water. The new product can e.g. B. found as a textile auxiliary application.
The following procedure can be used to prepare the condensation product used as the starting material: 72.6 parts of coconut fatty acid-N-methylolamide and 30.9 parts of phenol are dissolved in 200 parts of glacial acetic acid, 72.6 parts of dehydrated zinc chloride are added and the mixture is heated for 24 hours on 45 to 50. Washed with water and freed from small amounts of unchanged phenol by blowing off with steam, the product, a soft mass, can be thinned with water after it has been dissolved in an alcoholic solution of galium hydroxide.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH242605T | 1946-05-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH242605A true CH242605A (en) | 1946-05-31 |
Family
ID=4463049
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH242605D CH242605A (en) | 1946-05-31 | 1944-05-10 | Process for the preparation of a new derivative of a ring-substituted aromatic oxy compound. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH242605A (en) |
-
1944
- 1944-05-10 CH CH242605D patent/CH242605A/en unknown
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