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DE1031787B - Process for the preparation of enol derivatives of ª † - (ª ‰ -ionylidene) -acetoacetic acid - Google Patents

Process for the preparation of enol derivatives of ª † - (ª ‰ -ionylidene) -acetoacetic acid

Info

Publication number
DE1031787B
DE1031787B DEF19932A DEF0019932A DE1031787B DE 1031787 B DE1031787 B DE 1031787B DE F19932 A DEF19932 A DE F19932A DE F0019932 A DEF0019932 A DE F0019932A DE 1031787 B DE1031787 B DE 1031787B
Authority
DE
Germany
Prior art keywords
ionylidene
acetoacetic acid
preparation
enol derivatives
vol
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.)
Pending
Application number
DEF19932A
Other languages
German (de)
Inventor
Dr Karl Eiter
Dr Ernst Truscheit
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Priority to DEF19932A priority Critical patent/DE1031787B/en
Publication of DE1031787B publication Critical patent/DE1031787B/en
Pending legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C403/00Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
    • C07C403/20Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by carboxyl groups or halides, anhydrides, or (thio)esters thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/16Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated

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

Description

Verfahren zur Herstellung von Enolderivaten der y-(ß-Jonyliden)-acetessigsäure Es ist bekannt, daß man y-Brom-ß-alkoxycrotonsäureester mit Aldehyden, wie Benzaldehyd oder Zimtaldehyd, nach dem Verfahren von R e f o r m a t s k y entsprechend der folgenden Gleichung zu stabilen Lactonen der allgemeinen Formell umsetzen kann. Es ist weiterhin bekannt, daß man die so erhaltenen Lactone durch Kochen mit Lauge in die Säuren der Formel I I überführen kann (D. G. F. R. K o s t e r m a n s , Rec. Trav. chim. Pays Bas, Bd. 70, 1951 S. 79; E. B. Reid u. a., Journal of the American Chemical Society, Bd. 73, 1951, S. 1054). Verwendet man für die Umsetzung als Aldehyd den Cyclopentenaldehyd, so erhält man aus dem Lacton bei der Verseifung die Oxysäure der Formel III Für das erfindungsgemäße Verfahren geeignete Enolderivate y-halogenierter Acetessigsäureester sind z. B. y-Brom-ß-äthoxycrotonsäureäthylester, y-Brom-ß-methoxycrotonsäureester, y-Brom-ß-acetoxVcrotonsäuremethylester, y-Brorn-ß-carbäthoxycrotonsäureester, y-Bromß-phenoxycrotonsäureester, y-Brom-ß-phenylmethoxycrotonsäureester, y-Brom-ß-benzoxycrotonsäureester.Process for the preparation of enol derivatives of y- (ß-Jonyliden) -acetoacetic acid It is known that y-bromo-ß-alkoxycrotonic acid esters with aldehydes, such as benzaldehyde or cinnamaldehyde, according to the process of R eformatsky according to the following equation to form stable lactones can implement general formally. It is also known that the lactones obtained in this way can be converted into the acids of the formula II by boiling with lye (DGFR K ostermans, Rec. Trav. Chim. Pays Bas, Vol. 70, 1951 p. 79; EB Reid et al., Journal of the American Chemical Society, Vol. 73, 1951, p. 1054). If cyclopentenaldehyde is used as the aldehyde for the reaction, the oxyacid of the formula III is obtained from the lactone in the saponification For the process according to the invention suitable enol derivatives y-halogenated acetoacetic acid esters are, for. B. ethyl y-bromo-ß-ethoxycrotonic acid ester, y-bromo-ß-methoxycrotonic acid ester, methyl y-bromo-ß-acetox-crotonic acid ester, y-bromine-ß-carbethoxycrotonic acid ester, y-bromo-phenoxycrotonic acid ester, y-bromo-ß-phenyl methoxy crotonic acid ester Bromo-ß-benzoxycrotonic acid ester.

Die Umsetzung kann unter den bekannten Bedingungen der Reformatsky-Synthese vorgenommen «erden, d. h., man setzt die beiden Ausgangssubstanzen, die (F. Kögl u. a., Rec. Trav. chim. Pays Bas, Bd. 69, 1950, S.729).The reaction can take place under the known conditions of the Reformatsky synthesis made «earth, d. That is, the two starting substances that (F. Kögl inter alia, Rec. Trav. chim. Pays Bas, vol. 69, 1950, p.729).

Es wurde nun gefunden, daß man Enolderivate y-halogenierter Acetessigsäureester mit ß-Jonon unter den Bedingungen der Reformatsky-Synthese zu den Enolderivaten der y-(ß-Jonyliden)-acetessigsäure umsetzen kann.It has now been found that enol derivatives of γ-halogenated acetoacetic acid esters can be used with ß-ionone under the conditions of the Reformatsky synthesis to the enol derivatives the y- (ß-Jonyliden) -acetoacetic acid can convert.

Das neue Verfahren, bei dem direkt die freie Säure über die Zwischenstufe des Lactons ohne eine Alkalibehandlung erhalten wird, kann durch das folgende Reaktionsschema dargestellt werden: erforderlichenfalls in einem inerten Lösungsmittel gelöst sein können, in Gegenwart von Zink um. Als Lösungsmittel verwendet man dabei vorteilhafterweise polare Lösungsmittel, wie Tetrahydrofuran oder Diäthyläther. Die Aufarbeitung kann ebenfalls in bekannter Weise erfolgen.The new process in which the free acid goes directly through the intermediate stage of the lactone is obtained without alkali treatment can be obtained by the following reaction scheme be shown: if necessary, be dissolved in an inert solvent can order in the presence of zinc. The solvent used here is advantageously polar solvents such as tetrahydrofuran or diethyl ether. The work-up can also take place in a known manner.

Es war sehr überraschend, daß man die Enolderivate der y-(ß-Jonyliden)-acetessigsäure nach dem erfindungsgemäßen Verfahren erhalten kann, da es bekannt ist, daß ß-Jonol-Verbindungen, auch wenn sie nur als Zwischenprodukte auftreten, sehr leicht durch Retrojonylidenumlagerung Wasser abspalten und in biologisch fast unwirksame Substanzen der Retro-Vitamin-A-Reihe übergehen (W. Oroshnik u. a., Journal of the American Chemical Society, Bd.74, 1952, S.295 und 3807; H. 0. Huisman u. a., Rec. Trav. chim. Pays Bas, Bd. 71, 1952, S. 899; C. D. Robeson u. a. Journal of the American Chemical Society, Bd. 77, 1955, S. 4111; P. Karrer und J. Kebrle, Helv. Chim. Acta, Bd. 35, 1952, S.2570 bis 2573, besonders S.2570, Abs. 1. Es war daher zu erwarten, daß die bei dem erfindungsgemäßen Verfahren intermediär entstehende Oxysäure diese Retroj ony lidenumlagerung eingehen würde. Verbindungen, die das Ergebnis einer derartigen Umlagerung sein würden, konnten jedoch nicht beobachtet werden.It was very surprising that the enol derivatives of γ- (ß-Jonyliden) -acetoacetic acid can be obtained by the process according to the invention, since it is known that ß-ionol compounds, even if they are only as intermediates occur very easily The retrojonylid rearrangement splits off water and converts it into biologically almost inactive substances skip the retro vitamin A series (W. Oroshnik et al., Journal of the American Chemical Society, Vol. 74, 1952, pp. 295 and 3807; H. 0. Huisman et al., Rec. Trav. chim. Pays Bas, Vol. 71, 1952, p. 899; C. D. Robeson et al. Journal of the American Chemical Society, Vol. 77, 1955, p. 4111; P. Karrer and J. Kebrle, Helv. Chim. Acta, vol. 35, 1952, pp.2570 to 2573, especially p.2570, para. 1. It was therefore to be expected that the in the process according to the invention intermediate oxyacid this retroj ony lidenal rearrangement would enter. Compounds that are the result of such However, rearrangement could not be observed.

Aus J. Am. Chem. Soc., Bd. 77, 1955, S. 5166j5167, war es zwar bekannt, daß man bei der Wasserabspaltung aus bestimmten ungesättigten Alkoholen, die als Vorprodukte in der Vitamin -A-Synthese verwendet werden können, vermeiden kann, das Retro-Vitamin .AAcetat zu erhalten, wenn man unter neutralen Bedingungen arbeitet. Jedoch handelt es sich bei den dort verwendeten Verbindungen nicht um ß-Jonolverbindungen.From J. Am. Chem. Soc., Vol. 77, 1955, pp. 5166j5167, it was known that in the elimination of water from certain unsaturated alcohols that can be used as precursors in the vitamin A synthesis, the retro- Obtaining vitamin AA acetate when working under neutral conditions. However, the compounds used there are not ß-ionol compounds.

Die nach dem neuen Verfahren erhaltenen Verbindungen können als Zwischenprodukte für die Synthese von Vitamin-A-aktiven Verbindungen verwendet werden. Beispiel In einem Dreihalskolben mit Rührer, Rückflußkühler und Stickstoffeinleitungsrohr werden 3 g Zinkstaub mit verdünnter H Cl angeätzt und mit Jod aktiviert und 24,8 g frisch destilliertes ß-Jonon, 25 g y-Brom-ß-äthoxycrotonsäureäthylester in 35 ml absolutem Tetrahydrofuran gelöst, eingebracht. Nun wird die Mischung zum Sieden erhitzt, wobei eine heftige Reaktion unter Grünfärbung der Lösung eintritt. Hierauf werden die restlichen 7 g Zinkstaub in kleinen Anteilen nach dem Abklingen der Hauptreaktion zugesetzt, und nach der letzten Zugabe von Zinkstaub wird das Gemisch noch 1 Stunde am Rückflußkühler zur Vollendung der Reaktion erhitzt. Nach dem Entfernen des größten Teiles des Tetrahydrofurans im Vakuum wird die Mischung mit Äther versetzt und wiederholt mit kaltgesättigter Ammonchloridlösung ausgeschüttelt. Nach dem Abtrennen und Trocknen der ätherischen Phase wird der Äther abgedampft, der Rückstand mit Petroläther versetzt und im Eisschrank kristallisiert. Nach nochmaligem Umlösen werden 4 g einer etwas grünstichigen Verbindung vom Schmp. 131 bis 135°C erhalten.The compounds obtained by the new process can be used as intermediates used for the synthesis of vitamin A active compounds. Example In a three-necked flask equipped with a stirrer, reflux condenser and nitrogen inlet tube 3 g zinc dust etched with dilute H Cl and activated with iodine and 24.8 g fresh distilled ß-ionone, 25 g of γ-bromo-ß-ethoxycrotonic acid ethyl ester in 35 ml of absolute Dissolved tetrahydrofuran, introduced. Now the mixture is heated to the boil, whereby a violent reaction occurs and the solution turns green. Then the remaining 7 g zinc dust in small portions after the main reaction has subsided added, and after the final addition of zinc dust, the mixture is still 1 hour heated on the reflux condenser to complete the reaction. After removing the largest Part of the tetrahydrofuran in vacuo, the mixture is mixed with ether and repeated extracted with cold saturated ammonium chloride solution. After separating and drying The ether is evaporated from the ethereal phase, and petroleum ether is added to the residue and crystallized in the refrigerator. After dissolving again, 4 g of one become something greenish compound of melting point 131 to 135 ° C obtained.

Der Abdampfrückstand der 'Mutterlauge wird in Äther gelöst und mit 100 ml 1 n-NaOH portionenweise ausgeschüttelt. Die ätherische Phase enthält das Unverseifbare und ergibt nach dem Abdampfen und Destillation im Hochvakuum (0,8 Torr) 1,9 g ß .gthoxycrotonsäureäthylester (Schmp. 32" C) und 13,4 g unverändertes ß-Jonon.The evaporation residue of the 'mother liquor is dissolved in ether and with 100 ml of 1N NaOH shaken out in portions. The etheric phase contains that Unsaponifiable and after evaporation and distillation in a high vacuum (0.8 Torr) 1.9 g of ethyl thoxycrotonate (melting point 32 "C) and 13.4 g of unchanged ß-Jonon.

Die wäßrig alkalische Phase wird mit 1 n-H, SO, kongosauer gemacht und mit Äther extrahiert. Nach dem Waschen mit Wasser, Trocknen und Abdampfen werden 5 g y-(ß-Jonyliden)-ß-äthoxycrotonsäure erhalten, die nach dem Umlösen aus Äther - Aceton - Petroläther den Schmp. 130 bis 135° C zeigte. The aqueous alkaline phase is made Congo acidic with 1NH , SO, and extracted with ether. After washing with water, drying and evaporation, 5 g of γ- (ß-jonylidene) -ß-ethoxycrotonic acid are obtained which, after dissolving from ether - acetone - petroleum ether, had a melting point of 130 to 135 ° C.

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung von Enolderivaten der y-(ß-Jonyliden)-acetessigsäure, dadurch gekennzeichnet, daß man Enolderivate y-halogenierter Acetessigester mit ß-Jonon unter den bekannten Bedingungen der Reformatsky-Synthese umsetzt. In Betracht gezogene Druckschriften: Deutsche Patentschriften Nr. 839 494, 839 496; USA.-Patentschriften Nr. 2 475 139, 2 540118, 2 576 103; J. Am. Chem. Soc., Bd.77, 1955, S.5166, 5167.PATENT CLAIM: Process for the preparation of enol derivatives of y- (ß-ionylidene) -acetoacetic acid, characterized in that enol derivatives of y-halogenated acetoacetic esters are reacted with ß-ionone under the known conditions of the Reformatsky synthesis. Considered publications: German Patent Nos. 839 494, 839 496; U.S. Patent Nos. 2,475,139, 2,540,118, 2,576,103 ; J. Am. Chem. Soc., Vol. 77, 1955, pp. 5166, 5167.
DEF19932A 1956-03-31 1956-03-31 Process for the preparation of enol derivatives of ª † - (ª ‰ -ionylidene) -acetoacetic acid Pending DE1031787B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEF19932A DE1031787B (en) 1956-03-31 1956-03-31 Process for the preparation of enol derivatives of ª † - (ª ‰ -ionylidene) -acetoacetic acid

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Application Number Priority Date Filing Date Title
DEF19932A DE1031787B (en) 1956-03-31 1956-03-31 Process for the preparation of enol derivatives of ª † - (ª ‰ -ionylidene) -acetoacetic acid

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DE1031787B true DE1031787B (en) 1958-06-12

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1064506B (en) 1957-03-23 1959-09-03 Bayer Ag Process for the preparation of enol derivatives of gamma- (beta-jonylidene) -acetoacetic acid
DE1075599B (en) * 1960-02-18 Farbenfabriken Bayer Aktien gesellschaft, Leverkusen-Bayerwerk Process for the preparation of 2-trans-p-Jonylidenessigsaure
US3038933A (en) * 1958-08-07 1962-06-12 Bayer Ag Process for the production of 2-trans-beta-ionylidene acetic acid

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2475139A (en) * 1946-02-27 1949-07-05 Hoffmann La Roche Process for the manufacture of pentaenes
US2540118A (en) * 1946-12-31 1951-02-06 Hoffmann La Roche Process for the manufacture of pentaenes
US2576103A (en) * 1946-12-24 1951-11-27 Eastman Kodak Co Synthesis of vitamin a active compounds containing repeated isoprene units
DE839496B (en) 1949-11-26 1952-04-10 F. Hoffmann-La Roche &. Co. Aktiengesellschaft, Basel (Schweiz) Process for the preparation of pentaenes (vitamin A or -ethers and -esters)

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2475139A (en) * 1946-02-27 1949-07-05 Hoffmann La Roche Process for the manufacture of pentaenes
US2576103A (en) * 1946-12-24 1951-11-27 Eastman Kodak Co Synthesis of vitamin a active compounds containing repeated isoprene units
US2540118A (en) * 1946-12-31 1951-02-06 Hoffmann La Roche Process for the manufacture of pentaenes
DE839496B (en) 1949-11-26 1952-04-10 F. Hoffmann-La Roche &. Co. Aktiengesellschaft, Basel (Schweiz) Process for the preparation of pentaenes (vitamin A or -ethers and -esters)
DE839494B (en) 1949-11-26 1952-04-10 F. Hoffmann-La Roche & Co. Aktiengesellschaft, Basel (Schweiz) Process for the production of pentaenes (vitamin A ethers)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1075599B (en) * 1960-02-18 Farbenfabriken Bayer Aktien gesellschaft, Leverkusen-Bayerwerk Process for the preparation of 2-trans-p-Jonylidenessigsaure
DE1064506B (en) 1957-03-23 1959-09-03 Bayer Ag Process for the preparation of enol derivatives of gamma- (beta-jonylidene) -acetoacetic acid
US3038933A (en) * 1958-08-07 1962-06-12 Bayer Ag Process for the production of 2-trans-beta-ionylidene acetic acid

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