CH191409A - Process for the preparation of a Py-3-oxytetrahydro-8-oxynaphthoquinoline. - Google Patents
Process for the preparation of a Py-3-oxytetrahydro-8-oxynaphthoquinoline.Info
- Publication number
- CH191409A CH191409A CH191409DA CH191409A CH 191409 A CH191409 A CH 191409A CH 191409D A CH191409D A CH 191409DA CH 191409 A CH191409 A CH 191409A
- Authority
- CH
- Switzerland
- Prior art keywords
- oxytetrahydro
- oxynaphthoquinoline
- preparation
- oxynaphthalene
- epichlorohydrin
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Py-3-Oxytetrahydro-8-oxynaphthoehinolins. Nach dem im Hauptpatent beschriebenen Verfahren erhält man das als Ausgangs stoff für die Farbstoffherstellung brauchbare Py - 3 - Oxytetrahydro - 7 - oxynaphthochinolin, wenn man 1-Amino - 5 - oxynaphthalin mit Epichlorhydrin kondensiert.
Wie nun weiter gefunden wurde, kann man in ganz analoger Weise ein Py-3- Oxytetrahydro - 8 - oxynaphthochinolin erhal ten, wenn man 1-Amino-6-oxynaphthalin mit Epichlorhydrin bei erhöhter Temperatur zur Umsetzung bringt. Der neue Endstoff dient ebenfalls als Ausgangsmaterial für die Her stellung von Farbstoffen. Beispiel: 160 Teile 1-Amino-6-oxynaphthalin wer den mit 500 Teilen Amylalkohol und 120 Teilen Epichlorhydrin innerhalb einer Stunde unter Rühren auf 125 bis<B>130'</B> erhitzt.
Man hält diese Temperatur etwa 8 Stunden, lässt erkalten, saugt dann den ausgeschiedenen Kristallbrei ab und wäscht mit Aceton nach. Es werden 138 Teile Chlorhydrat des Py-3- Oxytetrahydro -8- oxynaphthochinolins erhal ten = 54,6 % der Theorie. Das Chlorhydrat ist in Wasser leicht löslich; die daraus durch Fällung mit Natriumacetat und Umkristal- lisieren aus verdünntem Alkohol gewonnene Base hat den Fp 206 bis 207 .
Process for the preparation of a Py-3-oxytetrahydro-8-oxynaphthoehinoline. According to the process described in the main patent, Py - 3 - oxytetrahydro - 7 - oxynaphthoquinoline, useful as a starting material for dye production, is obtained when 1-amino - 5 - oxynaphthalene is condensed with epichlorohydrin.
As has now been found further, a Py-3-oxytetrahydro-8-oxynaphthoquinoline can be obtained in a very analogous manner if 1-amino-6-oxynaphthalene is reacted with epichlorohydrin at elevated temperature. The new end product also serves as the starting material for the manufacture of dyes. Example: 160 parts of 1-amino-6-oxynaphthalene are heated with 500 parts of amyl alcohol and 120 parts of epichlorohydrin to 125 to 130 'within one hour while stirring.
This temperature is kept for about 8 hours, allowed to cool, then the precipitated crystal pulp is suctioned off and washed with acetone. There are 138 parts of py-3-oxytetrahydro-8-oxynaphthoquinoline hydrate obtained = 54.6% of theory. The chlorine hydrate is easily soluble in water; the base obtained therefrom by precipitation with sodium acetate and recrystallization from dilute alcohol has mp 206 to 207.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE191409X | 1935-02-20 | ||
CH186845T | 1935-11-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH191409A true CH191409A (en) | 1937-06-15 |
Family
ID=25721419
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH191409D CH191409A (en) | 1935-02-20 | 1935-11-12 | Process for the preparation of a Py-3-oxytetrahydro-8-oxynaphthoquinoline. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH191409A (en) |
-
1935
- 1935-11-12 CH CH191409D patent/CH191409A/en unknown
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