CH269410A - Process for the representation of a basic ether. - Google Patents
Process for the representation of a basic ether.Info
- Publication number
- CH269410A CH269410A CH269410DA CH269410A CH 269410 A CH269410 A CH 269410A CH 269410D A CH269410D A CH 269410DA CH 269410 A CH269410 A CH 269410A
- Authority
- CH
- Switzerland
- Prior art keywords
- ether
- representation
- compound
- basic
- basic ether
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/06—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton from hydroxy amines by reactions involving the etherification or esterification of hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
- C07C217/08—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines basischen Äthers. Gegenstand vorliegenden Patentes ist ein Verfahren zur Darstellung eines basischen :ltüers. Das Verfahren ist dadurch gekenn- zeiehnet, dass man eine Verbindung der Formel
EMI0001.0004
auf eine Verbindung der Formel
EMI0001.0006
worin 1 und Y zwei reaktionsfähige, mit Aus nahme eines in einem von ihnen enthaltenen Sauerstoffatoms, sich bei der Reaktion abspal tende Reste bedeuten, einwirken lässt.
Die erhaltene neue Verbindung, der n-Pro- pyl - cycloli exyl-carbin-,'-climethylamino-äthy 1 ätlier, siedet bei<B>126-1310</B> unter 12 mm Druck. Sie soll therapeutische Verwendung finden. <I>Beispiel:</I> Zu einer Suspension von 4 Teilen pulveri siertem Natriumamid in 60 Teilen absolutem Benzol werden<B>15,6</B> Teile n-Propyl-cy clohexyl- carbinol zugetropft und 1 Stunde bei 60 ge rührt.
Dann werden 10,8 Teile ss-Dimethyl- amino-äthylehlorid zugegeben und das Ganze 5 Stunden unter Rückfloss und Rühren er hitzt. Nach dem Abkühlen wird mit Wasser versetzt und mit. 10o/oiger Salzsäure mehrmals ausgeschüttelt. Die vereinigten salzsauren Aus züge werden mit Pottasche alkalisch gestellt, die ausgeschiedene Base in Äther aufgenom men, die Ätherlösung mit konzentrierter Pott aschelösung gewaschen, über Natriumsulfat getrocknet und der Äther abgedampft. Der als Rückstand erhaltene basische Äther siedet bei 126-131 unter 12 mm Druck.
Zum gleichen Endprodukt gelangt man auch, wenn man einen reaktionsfähigen Ester des n-Propyl-cyclohexyl-carbinols, z. B. ein Halogenid, in Gegenwart säurebindender Mit tel mit ss-Dim.ethylamino-äthanol zur Umset zung bringt.
Process for the representation of a basic ether. The subject of the present patent is a method for the preparation of a basic: oil. The process is characterized in that a compound of the formula
EMI0001.0004
to a compound of the formula
EMI0001.0006
wherein 1 and Y are two reactive, with the exception of one oxygen atom contained in one of them, are radicals which split off during the reaction, can act.
The new compound obtained, the n-propyl-cycloli exyl-carbin-, '- climethylamino-ethy1 ätlier, boils at 126-1310 under 12 mm pressure. It should find therapeutic use. <I> Example: </I> <B> 15.6 </B> parts of n-propylcyclohexylcarbinol are added dropwise to a suspension of 4 parts of powdered sodium amide in 60 parts of absolute benzene and the mixture is 60 parts for 1 hour stirs.
Then 10.8 parts of β-dimethylamino-ethyl chloride are added and the whole thing is heated under reflux and stirring for 5 hours. After cooling, water is added and. 10% hydrochloric acid extracted several times. The combined hydrochloric acid extracts are made alkaline with potash, the precipitated base is taken up in ether, the ethereal solution is washed with concentrated potash solution, dried over sodium sulfate and the ether is evaporated. The basic ether obtained as residue boils at 126-131 under 12 mm pressure.
The same end product is also obtained if a reactive ester of n-propyl-cyclohexyl-carbinol, eg. B. a halide in the presence of acid-binding agents with ss-Dim.ethylamino-ethanol to implement.
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH2397799X | 1942-09-23 | ||
CH269410T | 1943-08-11 | ||
GB15558/43A GB585994A (en) | 1943-09-22 | 1943-09-22 | Manufacture of aminoalkyl ethers and of quaternary ammonium compounds formed therefrom |
Publications (1)
Publication Number | Publication Date |
---|---|
CH269410A true CH269410A (en) | 1950-06-30 |
Family
ID=32110438
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH269410D CH269410A (en) | 1942-09-23 | 1943-08-11 | Process for the representation of a basic ether. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH269410A (en) |
-
1943
- 1943-08-11 CH CH269410D patent/CH269410A/en unknown
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