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DE905851C - Process for the preparation of ª-arylisopropylamines and their N-substitution products - Google Patents

Process for the preparation of ª-arylisopropylamines and their N-substitution products

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Publication number
DE905851C
DE905851C DET3011D DET0003011D DE905851C DE 905851 C DE905851 C DE 905851C DE T3011 D DET3011 D DE T3011D DE T0003011 D DET0003011 D DE T0003011D DE 905851 C DE905851 C DE 905851C
Authority
DE
Germany
Prior art keywords
hydrogenation
substitution products
arylisopropylamines
preparation
carried out
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
DET3011D
Other languages
German (de)
Inventor
Theodor H Temmler
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.)
THEODOR H TEMMLER
Original Assignee
THEODOR H TEMMLER
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 THEODOR H TEMMLER filed Critical THEODOR H TEMMLER
Priority to DET3011D priority Critical patent/DE905851C/en
Application granted granted Critical
Publication of DE905851C publication Critical patent/DE905851C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00Compounds containing amino groups bound to a carbon skeleton
    • C07C211/01Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
    • C07C211/26Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
    • C07C211/27Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring having amino groups linked to the six-membered aromatic ring by saturated carbon chains
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/02Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups

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

Description

Verfahren zur Herstellung von ß=Arylisopropylaminen und deren N-Substitutionsprodukten Es wurde ein Verfahren vorgeschlagen, nach dem die Hydrierung der Ester von i-Aryl-2-aminopropanolen und deren N-Su'bstitutionsprodukten zu i-Ar yl-2-amino-propanen unter Bedingungen einer intensivierten Katalyse durchgeführt werden soll, wobei in Besonderheit hochaktive Hydrierungskatalvsatoren wie auf hochaktiver Kohle kolloidal niedergeschlagenes Platin Verwendung finden sollen.Process for the production of ß = arylisopropylamines and their N-substitution products A process has been proposed according to which the hydrogenation of the esters of i-aryl-2-aminopropanols and their N-substitution products to i-aryl-2-aminopropanes under conditions an intensified catalysis is to be carried out, whereby in particular highly active Hydrogenation catalysts such as colloidally precipitated on highly active charcoal Platinum should be used.

Durch derartige Intensivierung der Hydrierung wurden die Ausbeuten an den gewünschten ß-Arylisopropylaminen und deren N-Substitutionsprodukten beim Arbeiten im technischen Maßstabe praktisch quantitativ, während sie unter den im Schrifttum bis dahin bekannt gewesenen Bedingungen infolge zu geringer Hydrierungsgeschwin digkeit beim Arbeiten im technischen Umfangenur sehr unvollständig verlaufen. Dabei war trotz der Verwendung aller für die Kernhydrierung des aromatischen Ringes günstigen Bedingungen die Bildung hydroaromatischer Amine hintangehalten worden, so daß die fl-Aral'kylamine in quantitativer Ausbeute erhalten werden.By intensifying the hydrogenation in this way, the yields were increased on the desired ß-arylisopropylamines and their N-substitution products in Works on a technical scale practically quantitative, while under the im Literature previously known conditions due to insufficient hydrogenation rate When working on a technical scale, it was only very incomplete. Included was favorable in spite of the use of all for the nuclear hydrogenation of the aromatic ring Conditions the formation of hydroaromatic amines have been prevented, so that the fl-Aral'kylamine can be obtained in quantitative yield.

Es wurde nun gefunden, daß die Intensivierung der Hydrierung dieser Ester der AminoaPkohole auch mit weniger aktiven Katalysatoren und ohne Anwendung von Druck gelingt, wenn man für eine möglichst weitgehende Vergrößerung der Oberfläche sorgt. Diese wird z. B. durch Verwendung von Hydriergefäßen mit vergrößertem 'Gasraum bei äußerst intensiver Durchmischung oder auch durch erhöhte Schüttei- oder Rührgeschwindigkeit erzielt. Die Hvdrierung führt dadurch in kürzester Zeit praktisch ohne Bildung von hydroaromatischen Aminen in quantitativer Ausbeute zu den gewünschten 8-Arallcylaminen. Der geringe. Nachteil. der sich durch .die erforderliche Vergrößerung der Apparatur ergibt, wird dadurch zum mindesten ausgeglichen. daß infolge der erzielten verbesserten Durchmischung der Hydrierflüssiglce.it mit dem Wasserstoff die Hvdrierzeit um ein Vielfaches, oft auf ein Zehntei und weniger, herabgedrückt wird, Das Verfahren ist in gleicher Weise bei Verwendung von Wasser wie von organischen Lösungsmitteln anwendbar. Selbstverstandlieh können auch neben dgr Aktivierung durch Vergrößerung der Oberfläche weitere zusätzliche Aktivierungsmittel benutzt werden. Das Verfahren ist auch - im technischen -1vI@aßstabe ohne Druck durchführbar. und es ist gleichgültig, ob die bei der Hydrierung der Ester entstandenen Säuren gepuffert oder neutralisiert werden oder unverändert in der Hi@drierlösun,g sich anreichern.It has now been found that the intensification of the hydrogenation of this Esters of amino alcohols also with less active catalysts and without application of pressure succeeds if one looks for the largest possible enlargement of the surface cares. This is z. B. by using hydrogenation vessels with an enlarged 'gas space at extremely intensive mixing or through increased pouring or stirring speed achieved. The hydrogenation thus leads in a very short time with practically no formation of hydroaromatic amines in quantitative yield to the desired 8-arallcylamines. The minor one. Disadvantage. which is characterized by the necessary enlargement of the apparatus results is at least compensated by this. that as a result of the improved Mixing the hydrogenation liquid with the hydrogen reduces the hydrogenation time by one Multiples, often to a tenth and less, are depressed, the procedure is Applicable in the same way when using water as with organic solvents. Of course, in addition to activation, the surface can also be enlarged further additional activating agents can be used. The procedure is also - feasible in the technical -1vI @ scale without pressure. and it does not matter whether the acids formed during the hydrogenation of the esters are buffered or neutralized become or be enriched unchanged in the hi @ drier solution.

Beispiel i ioo Teile des Hvdrochlorids vom Chlorpseudoephedrin, gelöst in 5o9 Teilen Alkohol, werden nach Zusatz eines 5°/aigen Palladium-Bariu.msulfat-Katalysators, enthaltend i g Palladium, bei 3 atü in einer Druckflasche von etwa 31/21 Inhalt mit Wasserstoff geschüttelt. Die Schüttelapparatur macht etwa iooHinundherbewegungen pro Minute. In 6 Minuten ist die für i Mol berechnete Menge Wasserstoff (1o,31) aufgenommen. Das Filtrat vom Katalysator wird,, zuletzt im Vakuum, eingedampft und bis zur Konstanz getrocknet. Auf diese Weise wird das Hydrochlorid des rechtsdrehenden Desoxyephedrins vom SchtnelzpunIct Uo bis 17,1' in einer Ausbeute von 991/o der Theorie erhalten. An Stelle des verwendeten .M1:chols kann man auch andere Lösungsmittel, z. B. Wasser, benutzen, wobei man das Volumen der Flüssigkeit auf 400 ccm verringern kann.EXAMPLE 100 parts of the hydrochloride of chloropseudoephedrine, dissolved in 509 parts of alcohol, are shaken with hydrogen at 3 atmospheres in a pressure bottle of about 31/21 content after the addition of a 5% palladium-barium sulfate catalyst containing palladium . The shaker makes about 100 movements per minute. The amount of hydrogen (10.31) calculated for i mol is absorbed in 6 minutes. The filtrate from the catalyst is, finally, evaporated in vacuo and dried until constant. In this way, the hydrochloride of the dextrorotatory deoxyephedrine from the point of contact Uo to 17.1 'is obtained in a yield of 991 / o of theory. Instead of the .M1: chols used, other solvents, e.g. B. water, use, whereby you can reduce the volume of the liquid to 400 ccm.

Beispiel 2 2 kg Chlorephedrinhydrochlorid werden nach Zugabe von 8 1 Äthylalkohol sowie eines i°/aigen Palladium-Bariumsulfat-Katalysators, enthaltend g Palladium, mittels eines schnelltourigen starken Führers mit -ooo Touren in der :Minute verrührt. Der Wasserstoff steht unter einem ganz geringen Lberdruck von etwa 25 mm Wassersäule. In etwa r Stunde ist die für i Mol berechnete Menge Wasserstoff absorbiert, und das Filtrat vom Katalysator wird, wie in Beispiel i angegeben, aufgearbeitet. Die Ausbeute an auf diese Weise er-. haltenem Desoxyephedrinlhydrochlorid ist praktisch quantitativ.Example 2 2 kg of chlorephedrine hydrochloride are added after adding 8 1 ethyl alcohol and an i ° / aigen palladium-barium sulfate catalyst containing g Palladium, by means of a fast-paced strong guide with -ooo tours in the : Stirred minute. The hydrogen is under a very low pressure of about 25 mm water column. In about r hour the amount of hydrogen calculated for i mole is absorbed, and the filtrate from the catalyst is, as indicated in Example i, worked up. The yield of this way. Holding deoxyephedrine hydrochloride comes in handy quantitatively.

Claims (3)

PATENTANSPRÜCHE: i. Verfahren zur Herstellung von ß-Arylisopropylaminen und deren N-Substitutionsprodukten durch katalytische Hydrierung der Ester von i Aryl-2-aminopropanolen bzw. deren l\T-Substitutionsprodukten, dadurch gekennzeichnet, daß man die Hydrierung unter weitgehender Vergrößerung der Oberfläche der Hvdrierlösun,g durch intensive Durchmischun:g oder durch erhöhte Schüttei- oder Rührgeschwindigkeit durchgeführt. PATENT CLAIMS: i. Process for the preparation of β-arylisopropylamines and their N-substitution products by catalytic hydrogenation of the esters of i Aryl-2-aminopropanols or their 1 \ T-substitution products, characterized in that that the hydrogenation is carried out with a substantial increase in the surface area of the Hvdrierlösun, g through intensive mixing: g or through increased pouring or stirring speed carried out. 2. Verfahren gemäß Anspruch i, dadurch gekennzeichnet, daß das Verfahren bei gewöhnlichem oder nur wenig e rhöhtem Druck durchgeführt wird. 2. The method according to claim i, characterized in that the method is carried out at normal or only slightly increased pressure. 3. Verfahren gemäß Anspruch i und 2, dadurch gekennzeichnet, daß übliche Hvdrierkatalysatoren der Platingruppe Verwendung finden.3. Procedure according to claim i and 2, characterized in that conventional hydrogenation catalysts the platinum group find use.
DET3011D 1943-12-21 1943-12-21 Process for the preparation of ª-arylisopropylamines and their N-substitution products Expired DE905851C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DET3011D DE905851C (en) 1943-12-21 1943-12-21 Process for the preparation of ª-arylisopropylamines and their N-substitution products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DET3011D DE905851C (en) 1943-12-21 1943-12-21 Process for the preparation of ª-arylisopropylamines and their N-substitution products

Publications (1)

Publication Number Publication Date
DE905851C true DE905851C (en) 1954-03-08

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Application Number Title Priority Date Filing Date
DET3011D Expired DE905851C (en) 1943-12-21 1943-12-21 Process for the preparation of ª-arylisopropylamines and their N-substitution products

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1230427B (en) * 1961-03-01 1966-12-15 Yamanouchi Pharma Co Ltd Process for the preparation of d-amphetamine

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1230427B (en) * 1961-03-01 1966-12-15 Yamanouchi Pharma Co Ltd Process for the preparation of d-amphetamine

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