CH175877A - Process for the preparation of 3-chloro-1-N- (Y-methoxy-B-oxypropyl) -n-butylaminobenzene. - Google Patents
Process for the preparation of 3-chloro-1-N- (Y-methoxy-B-oxypropyl) -n-butylaminobenzene.Info
- Publication number
- CH175877A CH175877A CH175877DA CH175877A CH 175877 A CH175877 A CH 175877A CH 175877D A CH175877D A CH 175877DA CH 175877 A CH175877 A CH 175877A
- Authority
- CH
- Switzerland
- Prior art keywords
- chloro
- butylaminobenzene
- oxypropyl
- preparation
- methoxy
- Prior art date
Links
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung Yon 3-Chlor-lL-N-(r-rnethoxy-ss-oxypropyl)- n-butylaminobenzol. Gemäss dem im Hauptpatent beschriebe nen Verfahren erhält man N-(r-Ä.thoxy-ss- oxypi-opyl)-n-butylaminobenzol, indem man Epichlorhydrin auf n-Butylaminobenzol bei erhöhter Temperatur zur Einwirkung bringt und das so erhaltene Produkt mit äthyl- alkoholischem Alkali weiter umsetzt.
Wie nun weiter gefunden wurde, kann man in ganz analoger Weise auch das 3- Chlor-l-N-(r - inethoxy-/3- o.xypropyl)-n-butyl- aminobenzol herstellen, wenn man Epichlor- hydrin auf 3-Chloi--1-butylaminoberizol bei erhöhter Temperatur einwirken lässt und das so erhaltene Produkt mit methyl- alkoholischein Alkali umsetzt. Die neue Ver bindung soll als Zwischenprodukt für die Herstellung von Farbstoffen dienen.
<I>Beispiel:</I> <B>367</B> Teile 3-Chlor-l-butylaminobenzol werden mit 187 Teilen Epichlorhydrin wäh rend 5 Stunden auf 130-140 erhitzt. Nach dem Abkühlen setzt man eine Lösung von 90 gr Ätznatron in 1200 Teilen Methanol hinzu und kocht dann die Lösung einige Stunden am R,ückflusskühler. Die Aufarbei tung geschieht wie in Beispiel 1 des Haupt patentes. Es werden 310 Teile 3-Chlor-l- N(r-methoxy-(3-oxypropyl)n-b utylamin ob enzol erhalten. Kpi2=200-202 .
Method for the preparation of 3-chloro-IL-N- (r-methoxy-ss-oxypropyl) -n-butylaminobenzene. According to the process described in the main patent, N- (r-Ä.thoxy-ss- oxypi-opyl) -n-butylaminobenzene is obtained by exposing epichlorohydrin to n-butylaminobenzene at an elevated temperature and the product thus obtained with ethyl alcoholic alkali continues to react.
As has now also been found, 3-chloro-IN- (r-inethoxy- / 3-o.xypropyl) -n-butyl-aminobenzene can also be prepared in a completely analogous manner if epichlorohydrin is converted to 3-chloro Lets -1-butylaminoberizole act at an elevated temperature and the product thus obtained is reacted with methyl alcoholic alkali. The new connection will serve as an intermediate for the manufacture of dyes.
<I> Example: </I> <B> 367 </B> parts of 3-chloro-l-butylaminobenzene are heated to 130-140 for 5 hours with 187 parts of epichlorohydrin. After cooling, a solution of 90 grams of caustic soda in 1200 parts of methanol is added and the solution is then boiled for a few hours on a reflux condenser. The processing takes place as in Example 1 of the main patent. 310 parts of 3-chloro-1- N (r-methoxy- (3-oxypropyl) n-butylamine ob enzene) are obtained. Kpi2 = 200-202.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE175877X | 1933-04-27 | ||
CH172363T | 1934-02-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH175877A true CH175877A (en) | 1935-03-15 |
Family
ID=25719181
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH175877D CH175877A (en) | 1933-04-27 | 1934-02-05 | Process for the preparation of 3-chloro-1-N- (Y-methoxy-B-oxypropyl) -n-butylaminobenzene. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH175877A (en) |
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1934
- 1934-02-05 CH CH175877D patent/CH175877A/en unknown
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