CH215079A - Process for the production of a cyclic carboxylic acid. - Google Patents
Process for the production of a cyclic carboxylic acid.Info
- Publication number
- CH215079A CH215079A CH215079DA CH215079A CH 215079 A CH215079 A CH 215079A CH 215079D A CH215079D A CH 215079DA CH 215079 A CH215079 A CH 215079A
- Authority
- CH
- Switzerland
- Prior art keywords
- carboxylic acid
- acid
- production
- bromobenzanthrone
- cyclic carboxylic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/02—Benzathrones
- C09B3/06—Preparation from starting materials already containing the benzanthrone nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 212430. Verfahren zur Herstellung einer cyclischen Carbonsäure. Im Hauptpatent ist ein Verfahren zur Her stellung einer Kupferphthalocyanintetracar- bonsäure beschrieben, welches dadurch ge kennzeichnet ist, dass man Kupferphthalo- cyanin in einer geschmolzenen Mischung von wasserfreiem Aluminiumchlorid und Alkali halogenid mit Phosgen umsetzt und das er haltene Säurechlorid durch Einwirkenlassen von Wasser in die freie Carbonsäure über führt.
Es wurde nun gefunden, dass man eine Bz1- Brombenzanthronmonocarbonsäure er hält, wenn man Bzl-Brombenzanthron in einer geschmolzenen Mischung von wasser freiem Aluminiumchlorid und Alkalihalo- genid mit Phosgen umsetzt und das erhal tene Säurechlorid durch Einwirkenlassen von Wasser in die freie Carbonsäure über führt.
Die so erhältliche Bzl-Brombenzanthron- monocarbonsäure ist ein wertvolles Zwischen produkt zur Herstellung von Farbstoffen. .Beispiel: In eine geschmolzene Mischung von 20 Gewichtsteilen Bz1-Brombenzanthron, 180 Gewichtsteilen wasserfreiem Aluminium chlorid, 20 CTewichtsteilen Kaliumchlorid und 10 Gewichtsteilen Natriumchlorid wird bei 155 bis<B>160'</B> C unter Rühren so lange ein langsamer Strom von Phosgen eingeleitet, bis eine Probe der Umsetzungsmischung voll kommen in verdünnter Natronlauge löslich ist.
Dann lässt man etwas abkühlen, giesst die Masse auf Eis, saugt die ausgeschiedene gelbe Verbindung ab, wäscht sie mit ver dünnter wässriger Salzsäure, dann mit Was ser kräftig aus und trocknet sie.
Es wird so eine Bzl-Brombenzanthron- carbonsäure erhalten, die, nach dem Umkri- stallisieren, von<B>300'</B> C ab sich allmählich zersetzt. Sie löst sich in starker Schwefel säure mit rotoranger und in verdünnten wässrigen Alkalihydrogyden mit gelber Farbe.
An Stelle einer Mischung von Kalium- chlorid und Natriumbromid können auch Ge mische anderer Alkalihalogenide oder auch ein Alkalihalogenid allein verwendet werden.
Additional patent to main patent No. 212430. Process for the production of a cyclic carboxylic acid. In the main patent, a process for the preparation of a copper phthalocyanine tetracarboxylic acid is described, which is characterized in that copper phthalocyanine in a molten mixture of anhydrous aluminum chloride and alkali halide is reacted with phosgene and the acid chloride obtained is converted into the free by exposure to water Carboxylic acid over leads.
It has now been found that a Bz1-bromobenzanthrone monocarboxylic acid is obtained if Bzl-bromobenzanthrone is reacted with phosgene in a molten mixture of anhydrous aluminum chloride and alkali halide and the acid chloride obtained is converted into the free carboxylic acid by exposure to water.
The Bzl-bromobenzanthrone monocarboxylic acid that can be obtained in this way is a valuable intermediate for the production of dyes. Example: In a molten mixture of 20 parts by weight of Bz1-bromobenzanthrone, 180 parts by weight of anhydrous aluminum chloride, 20 parts by weight of potassium chloride and 10 parts by weight of sodium chloride, a slow flow of phosgene is added at 155 to 160 ° C while stirring initiated until a sample of the reaction mixture come completely soluble in dilute sodium hydroxide solution.
Then it is allowed to cool a little, the mass is poured onto ice, the yellow compound which has precipitated is filtered off with suction, washed with dilute aqueous hydrochloric acid, then with water vigorously and dried.
A Bzl-bromobenzanthrone carboxylic acid is thus obtained which, after recrystallization, gradually decomposes from <B> 300 '</B> C above. It dissolves in strong sulfuric acid with red-orange color and in dilute aqueous alkali hydrogen with yellow color.
Instead of a mixture of potassium chloride and sodium bromide, mixtures of other alkali halides or an alkali halide alone can also be used.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE215079X | 1938-02-15 | ||
CH212430T | 1939-02-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH215079A true CH215079A (en) | 1941-05-31 |
Family
ID=25725271
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH215079D CH215079A (en) | 1938-02-15 | 1939-02-14 | Process for the production of a cyclic carboxylic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH215079A (en) |
-
1939
- 1939-02-14 CH CH215079D patent/CH215079A/en unknown
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