DE505798C - Process for the preparation of 2,4-dioxyquinolines - Google Patents

Process for the preparation of 2,4-dioxyquinolines

Info

Publication number
DE505798C
DE505798C DEI36989D DEI0036989D DE505798C DE 505798 C DE505798 C DE 505798C DE I36989 D DEI36989 D DE I36989D DE I0036989 D DEI0036989 D DE I0036989D DE 505798 C DE505798 C DE 505798C
Authority
DE
Germany
Prior art keywords
parts
dioxyquinolines
preparation
reaction
alcohol
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
DEI36989D
Other languages
German (de)
Inventor
Dr Hans Kaemmerer
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 DEI36989D priority Critical patent/DE505798C/en
Application granted granted Critical
Publication of DE505798C publication Critical patent/DE505798C/en
Expired legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Verfahren zur Darstellung von 2,4-Dioxychinolinen Es ist bekannt, 2, 4-Dioxychinol.ine in der Weise herzustellen, daß man Malonester oder dessen Alkyl- oder Arylderivate mit arornatisehen Aminen im ungefähren Verhältnis ihrer Molekulargewichte erhitzt.Process for the preparation of 2,4-dioxyquinolines It is known 2, 4-Dioxychinol.ine in such a way that one malonic ester or its alkyl or aryl derivatives with aromatic amines in the approximate ratio of their molecular weights heated.

Es wurde nun gefunden, daß man 2, 4-Dioxychinoline in vorzüglicher Ausbeute und in reiner Form erhalten kann, wenn man die Kondensation der Malonester mit aromatisehen Aminen in einem hochsiedenden Lösungsmittel vornimmt, wobei man vorteilhaft den bei der Reaktion entstehenden Alkohol während der Reaktion abdestillieren läßt.It has now been found that 2, 4-Dioxyquinolines in excellent Yield and can be obtained in pure form if the condensation of the malonic ester with aromatic amines in a high-boiling solvent, whereby one advantageous to distill off the alcohol formed in the reaction during the reaction leaves.

Da hierbei eine Überhitzung der Reaktionslösung nicht stattfindet, wird bei dem neuen Verfahren eine erhebliche Steigerung der Ausbeute gegenüber der Umsetzung in Ab- wesenheit von Lösungsmitteln erzielt. Beispiel i 75 Teile a-Naphthylamin werden mit ioo Teilen Malonsäurediäthylester unter Zusatz von 2oo Teilen Nitrobenzol zum Sieden erhitzt, wobei man die Länge des Luftkühlers so wählt, daß unter Rückfluß des Nitrobenzols der Alkohol abdestillieren kann. Man hält das Reaktionsgemisch etwa 3 Stunden lang im Sieden; nach dieser Zeit sind etwa 4o bis 5o Teile Alkohol abdestilliert. Das entstandene 2, 4-Dioxynaphthochinolin scheidet sich aus der Lösung in reiner Form ab. Nach dem Erkalten wird abgepreßt, die letzten Reste des Nitrobenzols werden durch Destillation m-it Wasserdampf entfernt. Man erhält etwa 107 Teile des 2, 4-Dioxynaphthochinolins, das auch als 2,4-Diketo-i,2,3, 4-tetrahydrochinolin betrachtet werden kann. Es ist nahezu vollkommen in verdünnter Natronlauge löslich und kann ohne weitere Reinigung zu Umsetzungen z. B. zur Darstellung von Azofarbstoffen verwendet werden. Beispiel 2 54 Teile m-Toluidin werden mit ioo Teilen Malonsäurediäthylester und 2.ooTeilen Nitrobenz01 3 bis 4 Stunden lang zum Sieden erhitzt, wobei man den abgespaltenen Alkohol abdestillieren läßt. Nach dem Erkalten saugt man ab und arbeitet, wie in Beispiel i angegeben, auf. Man erhält in guter Ausbeute das im Benzolkern methylierte 2,4-Dioxybenzochinolin. Beispiel 3 i5o Teile a-Naphthylarnin werden mit 5oo Teilen Malonsäurediäthylester unter Rückfluß zum Sieden erhitzt. Den bei der Reaktion abgespaltenen Alkohol läßt man dabei durch Wahl eines Luftkühlers von geeigneter Länge ab#destillieren. Man erhält 2,4-Dioxynaphthochinolin in reiner Form und in nahezu quantitativer Ausbeute.Here, since overheating of the reaction solution does not take place, a substantial increase in the yield to the reaction in the absence of solvents being achieved in the new method. Example i 75 parts of a-naphthylamine are heated to boiling with 100 parts of diethyl malonate with the addition of 200 parts of nitrobenzene, the length of the air cooler being chosen so that the alcohol can distill off under reflux of the nitrobenzene. The reaction mixture is kept boiling for about 3 hours; after this time about 40 to 50 parts of alcohol have distilled off. The resulting 2,4-dioxynaphthoquinoline separates out of the solution in pure form. After cooling, it is pressed out, the last residues of the nitrobenzene are removed by distillation with steam. About 107 parts of 2,4-dioxynaphthoquinoline are obtained, which can also be regarded as 2,4-diketo-i, 2,3,4-tetrahydroquinoline. It is almost completely soluble in dilute sodium hydroxide solution and can be used without further purification for reactions such. B. used to represent azo dyes. Example 2 54 parts of m-toluidine are heated to boiling with 100 parts of diethyl malonate and 2oo parts of nitrobenz01 for 3 to 4 hours, the alcohol which has been split off being allowed to distill off. After cooling, it is suctioned off and worked on, as indicated in example i. The 2,4-dioxybenzoquinoline methylated in the benzene nucleus is obtained in good yield. EXAMPLE 3 150 parts of a-naphthylamine are refluxed with 500 parts of diethyl malonate. The alcohol split off in the reaction is allowed to distill off by choosing an air cooler of a suitable length. 2,4-Dioxynaphthoquinoline is obtained in pure form and in an almost quantitative yield.

Claims (1)

PATFNTANSPRUCII - Verfahren zur Darstellung von 2,4-Dioxvchinolinen aus Malonsäureestern un,1 aromatischen Aminen, dadurch gekennzeichnet, daß man die Kondensation der Malonester mit aromatischen Aminen in einem hochsiedenden Lösungsmittel vorn.immt.PATFNTANSPRUCII - Process for the preparation of 2,4-dioxvquinolines from malonic esters and 1 aromatic amines, characterized in that the condensation of the malonic esters with aromatic amines in a high-boiling solvent is carried out.
DEI36989D 1929-02-05 1929-02-05 Process for the preparation of 2,4-dioxyquinolines Expired DE505798C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI36989D DE505798C (en) 1929-02-05 1929-02-05 Process for the preparation of 2,4-dioxyquinolines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI36989D DE505798C (en) 1929-02-05 1929-02-05 Process for the preparation of 2,4-dioxyquinolines

Publications (1)

Publication Number Publication Date
DE505798C true DE505798C (en) 1930-08-25

Family

ID=7189400

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI36989D Expired DE505798C (en) 1929-02-05 1929-02-05 Process for the preparation of 2,4-dioxyquinolines

Country Status (1)

Country Link
DE (1) DE505798C (en)

Similar Documents

Publication Publication Date Title
DE505475C (en) Process for the separation of condensation products from aromatic bases and hydroaromatic ring ketones of the cyclohexanone series
DE505798C (en) Process for the preparation of 2,4-dioxyquinolines
DE697139C (en) Process for the recovery of phenols in the extraction of oils with phenols
DE490418C (en) Process for the preparation of basic ethers of the acridine series
DE693988C (en) Process for the preparation of aliphatic ketoanils
DE656132C (en) Process for dismantling stand oils
CH145150A (en) Process for the preparation of quinoline derivatives.
DE575362C (en) Process for the preparation of acidic wool dyes of the anthraquinone series
DE657779C (en) Process for the preparation of 2, 2'-dimethyl-4, 4'-dioxy-p-phenanthroline
DE712002C (en) Process for the production of alkyd resins
DE646299C (en) Process for the preparation of alkylamines of the anthraquinone series
AT149348B (en) Process for the preparation of polymethine dyes.
DE420148C (en) Process for the preparation of triarylmethane dyes
DE742257C (en) Process for the preparation of N-aryl-3-oxypyrrolidines
DE545195C (en) Process for the preparation of ar-tetrahydronaphthola ethers
DE641799C (en) Process for the preparation of polymethine dyes
DE896343C (en) Process for the preparation of ª † -valerolactone
DE565481C (en) Process for the preparation of unsaturated fatty acids
AT144040B (en) Process for the preparation of derivatives of benzylisoquinoline.
DE658955C (en) Process for the production of mineral oil-soluble castor oil
DE710276C (en) Process for the preparation of ª ‰ -Merkaptoalkylaminen
DE609844C (en) Process for the production of condensation products
DE737053C (en) Process for the preparation of pseudocyanine dyes
DE934887C (en) Process for the separation and recovery of naphthenic acids from mixtures containing naphthenic acid
DE666803C (en) Process for the production of liquid phosphatide products, especially suitable for soap production, at normal temperature