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DE499149C - Process for the preparation of compounds of the anthracene series - Google Patents

Process for the preparation of compounds of the anthracene series

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Publication number
DE499149C
DE499149C DEI31980D DEI0031980D DE499149C DE 499149 C DE499149 C DE 499149C DE I31980 D DEI31980 D DE I31980D DE I0031980 D DEI0031980 D DE I0031980D DE 499149 C DE499149 C DE 499149C
Authority
DE
Germany
Prior art keywords
compounds
preparation
sulfuric acid
yellow
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
DEI31980D
Other languages
German (de)
Inventor
Dr Karl Schirmacher
Dr Hans Schlichenmaier
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI31980D priority Critical patent/DE499149C/en
Application granted granted Critical
Publication of DE499149C publication Critical patent/DE499149C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C13/00Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
    • C07C13/28Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
    • C07C13/32Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
    • C07C13/54Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings
    • C07C13/573Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings with three six-membered rings
    • C07C13/58Completely or partially hydrogenated anthracenes

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Verfahren zur Darstellung von Verbindungen der Anthracenreihe . Es wurde gefunden, daß man neue Verbindungen .der Anthracenrdhe -erhält, ' weain man i, z, 3, q.-Tetrahydroanthrachinone mit nitrierenden Mitteln behandelt. Unerwarteterweise findet hierbei keine D@ehydrierung statt, sondern man erhält Nitrotetrahydroanthrachinone, welche die Nitrogruppen -im aromatischen Kerne und 'den tefrahydrierten Ring unverändert enthalten. So .erhält man aus dem i, z, 3, q-Tetrahydroanthrachinoü selbst ein Gemisch, das neben wenig 3-Nitroverbindung in ganz überwiegender Menge aus dem # -tr -a-Nitro - 1, 2, 3, 4 - Tetrahydroanthrachinon besteht. Daß das in geringerer Menge erhaltene Nitroprodukt der Formel entspricht, ergibt sich daraus, daß die daraus durch Reduktion und Acetylierung hergestellte Acetaminoverbindung identisch ist mit der durch Hydrierung von 3-Aoetaminoanthrachinon erhaltenen Verbindung, der zweifellos folgende Konstitution. zukommt: Diese glatte Nitrierung ist überraschend, da, wie Versuche gezeigt haben, z. B. konzentrierte Schwefelsäure allein auf Tetrahydroa nt, 'hrachinone dehydrierend wirkit# die Einwirkung von Brom aber zu Bromderivaten führt, die das Brom im hydrierten Kerne enthalten und sehr unbeständig sind. Sie geben leicht Bromwassenstoff ab und gehen in die entsprechenden Anthrachinorne@ über. Es war daher zu erwarben, da.ß Salpetersäure bzw. Salpeterschwefelsäure zum, mindesten ebenso dehydrierend wirken würden wie Brom oder Schwefelsäure.Process for the preparation of compounds of the anthracene series. It has been found that new compounds of the anthracene earth are obtained by treating i, z, 3, q.-tetrahydroanthraquinones with nitrating agents. Unexpectedly, no dehydrogenation takes place here, but nitrotetrahydroanthraquinones which contain unchanged the nitro groups in the aromatic nucleus and the tetrahydrated ring. Thus, a mixture is obtained from the i, z, 3, q-tetrahydroanthraquinone itself which, in addition to a little 3-nitro compound, consists in the predominant amount of the # -tr -a-nitro - 1, 2, 3, 4 - tetrahydroanthraquinone. That the nitro product of the formula obtained in smaller quantities it follows that the acetamino compound produced therefrom by reduction and acetylation is identical to the compound obtained by hydrogenation of 3-aoetaminoanthraquinone, which undoubtedly has the following constitution. comes to: This smooth nitriding is surprising since, as tests have shown, e.g. B. concentrated sulfuric acid alone on tetrahydroa nt, 'hrachinone has a dehydrating effect, but the action of bromine leads to bromine derivatives which contain the bromine in the hydrogenated nucleus and are very unstable. They easily give off hydrogen bromide and go into the corresponding anthraquinones @. It was therefore to be acquired that nitric acid or nitric sulfuric acid would at least have as dehydrating effect as bromine or sulfuric acid.

Die neuen Verbindungen sollen als Ausgangsmaterialien für Farbstoffe und pharmazeutische Produkte Verwendung finden. R'aisptele 1. In 'ein Gemisch von 500 Volumteilen iooprozentiger Schwefelsäure und 6o V.olum- teilen Salpetersäure vom spezifischen Gewicht 1,4 werden bei 2o' i i o Gewichtsteile 1, 2, 3, ¢- Tetrahydroanthrachino.n so eilgetragen, daß die Temperatur auf 4o bis 5o° steigt und sich dabei hält. Ist alles Tetra@hydroanthrachihon eingetragen, so erstarrt die Masse zu einem hellgelben Kristallbrei, welcher sofort auf Eis gegeben wird. Das abgeschiedene hellgelb gefärbte Reaktionsprodukt wird abgesaugt und mit Sprit ausgekocht. Der Rückstand, welcher weitaus die Hauptmengie darstellt, wird aus Eiiseisisig umkristalliß#ert. Er wird in schön ausgebildeten grürngelhen Kristallene erhalten. Dieselben schmelzen bei i92°. Ihre Lösungsfarbe in konzentrierter Schw -efvelsäure ist rotgelb; behandelt man sie mit Natron- lauge und Hydrosulfit, so geben sie unter gleichzeitiger Reduktion der Nitrogruppe eine rotgelbe Lösung. In Wasser und Sprit sind sie sehr schwer, In Eisessig ziemlich löslich. Es liegt, wige in der Einletung auseimander- gesetzt, das Nitroderivat folgender Konstitu- tion vor. Aus der alkoholischen Mutterlauge kristallisiert beim Erkalten die isomene ß=Verbindung aus; dieselbe wird durch Ustalläsieren aus Petroläther, nötigenfalls unter Zusatz von etwas Tierkohle, eil schwach gelb gefärbten Kristallen erhalten. Dieselben lösen sich in konzentrierter Schwefelsäure schwach gelb, in Natronlauge und Hydrosulfit rotgelb. Die Verbindung schmilzt bei 133 biis 13q.° und ist in. heißem Sprit ziemlich lfls:Äch. 2. Zu .einer Lösung von 22,6 Gewichtstei- len 1, 2, 3, 4-Tetrahydro-7-m:ethylanihrachinon in 15o Volumtei'len Schwefelsäure werden bei 40 '.bis 50° 12 Volumteile Salpetersäure vom spezifischen Gewicht 1,4 einiropfen gelassen. Ist alles zwgelaufien, ;so wird Idas Reaktionspro- dukt auf Eis gegossen, abgesaugt und aus Sprit kristallisiert. Es stellt gelbe Kristalle dar; schmelzen bei 13J und läsen sich in konzentrierter Schwefelsäure gelbrot. Die Farbe der Lösung ih Natronlauge und Hydrosulfit ist gelbrot. In Alkohol und Eis- essig Ist die Verbdung ziemlich, in Xylol sehr leicht löslich. 3. 26,9 Gewichtsteile 1, 2, 3, q.-Tetrahydro- 8-acetylaminoanihraehinon (erbalten, aus dem nach Beispiel i Abs. i dargestellten 1, 2, 3, 4.- Tetrahydro-8-nitroanihrachlnon idurdh: Reduk- tion und Acetylilerung) wenden bei - 5° in ein Gemenge von 200 Volumteillen Mono- hydrat und i o Volumteilen Salpetersäume vom spezifischen Gewicht 1,4 ungetragen und das Reaktionsgemisch dann auf Eis gegossen. Der Niederschlag wird abgesaugt, durchAus- kochen mit Sprit von rotglefärbten Nübenpro- dukten befreit und aus Eisessig unikristalli- siert. Man erhält so orange gefärbte Kr@s-talle, welche sieh bei! 185° zerrsetzen und in kon-- zenirierter Schwefelsäure fasst farblos löslich sind. The new compounds are to be used as starting materials for dyes and pharmaceutical products. R'aisptele 1. In 'a mixture of 500 parts by volume 100 percent sulfuric acid and 60 vol. share nitric acid by specific gravity 1.4 at 2o 'iio parts by weight 1, 2, 3, ¢ - Tetrahydroanthrachino.n carried so quickly that the temperature rises to 4o to 5o ° and itself keeps doing it. Is everything Tetra @ hydroanthrachihon entered, the mass solidifies to one pale yellow crystal pulp, which immediately on ice is given. The separated light yellow colored reaction product is filtered off with suction and boiled with fuel. The residue, which is by far the main crowd, is recrystallized from iron ice. He will in beautifully formed greenish crystals obtain. They melt at i92 °. Her Solution paint in concentrated sulfuric acid is red-yellow; if you treat them with soda alkali and hydrosulphite, so put them under simultaneous reduction of the nitro group one red-yellow solution. Are in water and fuel they are very difficult, fairly soluble in glacial acetic acid. It lies apart in the inlet set, the nitro derivative of the following constituent tion before. The isomic ß = compound crystallizes out of the alcoholic mother liquor on cooling; it is obtained by staling out of petroleum ether, if necessary with the addition of some animal charcoal, partly pale yellow colored crystals. They dissolve weakly in concentrated sulfuric acid yellow, red-yellow in caustic soda and hydrosulfite. The compound melts at 133 to 13 ° and is pretty in. hot fuel lfls: Ahem. 2. To a solution of 22.6 parts by weight len 1, 2, 3, 4-tetrahydro-7-m: ethylanihrachinone Sulfuric acid is added in 150 parts by volume 40 'to 50 ° 12 parts by volume of nitric acid from specific gravity 1.4. If everything has failed, Ida's reaction Dukt poured on ice, vacuumed and off Fuel crystallizes. It represents yellow crystals dar; melt at 13J and let turns yellow-red in concentrated sulfuric acid. The color of the solution ih caustic soda and Hydrosulfite is yellow-red. In alcohol and ice vinegar is pretty much the compound in xylene very easily soluble. 3. 26.9 parts by weight of 1, 2, 3, Q.-tetrahydro- 8-acetylaminoanihraehinone (inherited from the 1, 2, 3, 4.- Tetrahydro-8-nitroanihrachlnon idurdh: Reduk- tion and acetylation) turn at - 5 ° in a mixture of 200 parts by volume mono- hydrate and io parts by volume nitric fringes from specific gravity 1.4 never worn and that The reaction mixture was then poured onto ice. The precipitate is sucked off, by cooking with gasoline from red-colored beet products and made of glacial acetic acid unicrystalline sated. Orange colored crystals are obtained in this way, which watch! Distort 185 ° and in con- Zenirated sulfuric acid is colorless and soluble are.

Claims (1)

PATENTANSPRUCH:
Verfahren zur Darstellung von Verbindungen der Anthmcenreiuhe, darit bestehend, daß man 1, 2, 3, d.-Tetrahydroanthrachinon, dessen Homologe oder Substitutlonsprodukte mit nitrierenden Mitteln behandelt,
PATENT CLAIM:
Process for the preparation of compounds of the anthropogenic series consisting of treating 1, 2, 3, d.-tetrahydroanthraquinone, its homologues or substitution products with nitrating agents,
DEI31980D 1927-08-18 1927-08-19 Process for the preparation of compounds of the anthracene series Expired DE499149C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI31980D DE499149C (en) 1927-08-18 1927-08-19 Process for the preparation of compounds of the anthracene series

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE295943X 1927-08-18
DEI31980D DE499149C (en) 1927-08-18 1927-08-19 Process for the preparation of compounds of the anthracene series

Publications (1)

Publication Number Publication Date
DE499149C true DE499149C (en) 1930-06-13

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
DEI31980D Expired DE499149C (en) 1927-08-18 1927-08-19 Process for the preparation of compounds of the anthracene series

Country Status (1)

Country Link
DE (1) DE499149C (en)

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