3-Dimethylaminoacrolein

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3-Dimethylaminoacrolein
Names
Preferred IUPAC name
(2E)-3-(Dimethylamino)prop-2-enal
Other names
3-Dimethylaminopropenal
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.011.962 Edit this at Wikidata
EC Number
  • 213-157-7
UNII
  • InChI=1S/C5H9NO/c1-6(2)4-3-5-7/h3-5H,1-2H3/b4-3+
    Key: RRLMPLDPCKRASL-ONEGZZNKSA-N
  • CN(C)/C=C/C=O
Properties
C5H9NO
Molar mass 99.133 g·mol−1
Appearance Clear, faintly yellow[1] to dark brown liquid[2]
Density 0.99 g·cm−3 at 25°C[1]
Boiling point *91 °C at 0.1 kPa[1]
  • 133–144 °C[3]
  • 270–273 °C[2]
Soluble[3]
Solubility in methanol,[4] 1,2-dichloroethane[5] Soluble
Hazards
GHS labelling:
GHS05: Corrosive
Danger
H314
P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

3-Dimethylaminoacrolein is an organic compound with the formula Me2NC(H)=CHCHO. It is a pale yellow water-soluble liquid. The compound has a number of useful and unusual properties, e.g. it "causes a reversal of the hypnotic effect of morphine in mice" and has a "stimulating effect in humans".[3]

It is a stable and comparably nontoxic precursor for the genotoxic, mutagenic, and potentially carcinogenic malondialdehyde.[6] The compound can be thought of as vinylogous dimethylformamide (DMF) and combines the functionalities of an unsaturated aldehyde and an enamine. Therefore, 3-dimethylaminoacrolein and vinamidines derived therefrom (composed of vinylogous amidines) or vinamidinium salts (substituted 1,5-diazapentadienes)[7] can be used as reactive molecular building blocks for the formation of nitrogen-containing heterocycles, such as pyridines, pyrimidines, pyrroles or pyrazoles.[8]

Preparation

3-Dimethylaminoacrolein is obtained by the addition of dimethylamine to the triple bond of propynal (propargyl aldehyde) via a Reppe vinylation.[3]

Synthese of Dimethylaminoacrolein from propynal.
Synthese of Dimethylaminoacrolein from propynal.

Propynal is however an inappropriate starting material for industrial synthesis because of its tendency to explode.[9] Vinyl ethers (such as ethyl vinyl ether) are more suited.[10] They react with phosgene and dimethylformamide (which forms in-situ the Vilsmeier reagent) in 68% yield to 3-ethoxypropenylidene dimethylammonium chloride, an enol ether iminium salt. In the weakly alkaline medium, 3-dimethylaminoacrolein is formed therefrom, which cleaves dimethylamine to form propanedial upon exposure to strong bases (such as sodium hydroxide).

Synthesis of dimethylaminoacrolein as described by Arnold.
Synthesis of dimethylaminoacrolein as described by Arnold.

In an alternative route, isobutyl vinyl ether reacts with the iminium chloride derived from DMF and phosgene. The conversion can be implemented in a continuous process.[4] The iminium salt yields 3-dimethylaminoacrolein in dilute sodium hydroxide solution in 86% yield.[11]

Synthesis of 3-dimethylaminoacrolein via isobutylvinylether.
Synthesis of 3-dimethylaminoacrolein via isobutylvinylether.

Instead of phosgene, the iminium salt can also be prepared via an inorganic acid chloride, such as phosphoryl trichloride or an organic acid chloride, such as oxalyl chloride.

Use

Reactions with 3-dimethylaminoacrolein

3-Dimethylaminoacrolein can be used to introduce unsaturated and reactive C3 groups into CH-acidic and nucleophilic compounds.

The activated aldehyde group of 3-dimethylaminoacrolein reacts quantitatively with dialkyl sulfates such as dimethyl sulfate. The products are reactive but unstable[12] decompose at 110 °C back into the starting materials. The products can be easily transformed with nucleophiles such as alkoxides or amines into the corresponding vinylogous amide acetals or amidines.[13]

Reaktionen vinyloger Amidine nach Bredereck
Reaktionen vinyloger Amidine nach Bredereck

The stable 3-dimethylaminoacrolein dimethyl acetal is obtained by reaction with sodium methoxide in 62% yield. 3-Dimethylaminoacrolein can be reacted with CH-acidic compounds (such as malononitrile) to 1,3-butadiene derivatives or with cyclopentadiene to an aminofulvene.

With guanidine, 3-dimethylaminoacrolein forms almost quantitatively 2-aminopyrimidine.[4]

Synthese von 2-Aminopyrimidin aus 3-Dimethylaminoacrolein
Synthese von 2-Aminopyrimidin aus 3-Dimethylaminoacrolein

The amidine formed with 2-naphthylamine and the dimethyl sulfate adduct can be cyclized with sodium methoxide to give benzo[f]quinoline (1-azaphenanthrene).[14]

Synthese von Benzo[f]chinolin mit 3-Dimethylaminoacrolein
Synthese von Benzo[f]chinolin mit 3-Dimethylaminoacrolein

N-methylpyrrole forms the 3-(2-N-methylpyrrole)propenal with 3-dimethylaminoacrolein and POCl3 in 49% yield.[15]

Synthese von substituiertem Pyrrol
Synthese von substituiertem Pyrrol

Similarly, the preparation of an intermediate for the cholesterol lowering drug fluvastatin via the reaction of a fluoroaryl-substituted N-isopropylindole with 3-dimethylaminoacrolein and POCl3 proceeds similarly.[16][17]

Synthese einer Fluvastatin-Zwischenstufe mit 3-Dimethylaminoacrolein
Synthese einer Fluvastatin-Zwischenstufe mit 3-Dimethylaminoacrolein

Occasionally, the iminium salt from the reaction of the Vilsmeier reagent and the vinyl ether (a precursor of 3-dimethylaminopropenal) is directly used for synthesis, e. g. for pyrazoles.[18]

Pyrazolsynthese mit 3-Dimethylaminoacrolein
Pyrazolsynthese mit 3-Dimethylaminoacrolein

When hydrazine hydrate is used, a pyrazole parent body is formed in 84% yield.

Reactions to vinamidinium salts

The reaction of 3-dimethylaminoacrolein with dimethylammonium tetrafluoroborate produces virtually quantitatively the vinamidinium salt 3-dimethylaminoacrolein dimethyliminium tetrafluoroborate, which crystallizes better as the perchlorate salt. The salt reacts also with cyclopentadiene in the presence of sodium amide in liquid ammonia to give the aminofulvene derivative.[19]

The same vinamidinium salt 1,1,5,5-tetramethyl-1,5-diazapentadienium chloride is also formed in the reaction of 3-dimethylaminoacrolein with dimethylamine hydrochloride in 70% yield.[20] The two-step reaction of dimethylamine and 70% perchloric acid with 3-dimethylaminoacrolein forms the same iminium salt (herein referred to as 1,3-bis(dimethylamino)trimethinium perchlorate).[21]

Synthese des 1,3-Bis(dimethylamino)trimethinium perchlorats
Synthese des 1,3-Bis(dimethylamino)trimethinium perchlorats

Lactones (e.g. γ-butyrolactone) or cyclic ketones (such as cyclopentanone) form with the vinylamidinium salt of 3-dimethylaminoacrolein and dimethylamine hydrochloride the corresponding dienaminones in 91% and 88% yield.[22]

Reaktion von 3-Dimethylaminoacrolein mit gamma-Butyrolacton
Reaktion von 3-Dimethylaminoacrolein mit gamma-Butyrolacton

The vinamidinium salt 1,1,5,5-tetramethyl-1,5-diazapentadienium chloride reacts with heterocycles bearing CH-acidic groups to form the corresponding dienamines which can be cyclized with bases to form fused heteroaromatics, such as carbazoles, benzofurans or benzothiophenes.[7]

Synthese von Carbazolen und Benzothiophenen
Synthese von Carbazolen und Benzothiophenen

N-alkylpyrroles are obtained in good yield (86%) in the reaction of the vinamidinium salt with glycine esters,[23] substituted thiophenes (up to 87%) in the reaction with mercaptoacetic acid esters.[24]

Synthese von Thiophenen und Pyrrolen
Synthese von Thiophenen und Pyrrolen

The use of 3-dimethylaminoacrolein for the synthesis of 2-chloronicotinic acid (2-CNA) is of industrial interest as an important starting material for agrochemicals and pharmaceuticals. For this purpose, 3-dimethylaminoacrolein is reacted with cyanessigsäureethylester[25] to 2-chlornicotinsäureethylester or with cyanoacetic acid n-butyl ester to 2-Chlornicotinsäure-n-butyl ester[26] in a Knoevenagel reaction.

Synthese von 2-Chlornicotinsäure mit 3-Dimethylaminoacrolein
Synthese von 2-Chlornicotinsäure mit 3-Dimethylaminoacrolein

The resulting esters of 2-chloropyridine carboxylic acid can be hydrolyzed smoothly to 2-chloronicotinic acid.

Other reactions

It reacts weakly alkaline and gives with iron(III) chloride a deep red color.

Related compounds

  • (Z)-β-Aminoacrolein (H2NCH=CHCHO, CAS# 25186-34-9)[27]
  • (E)3-(N-Phenyl-N-methyl)aminoacrolein (PhNHCH=CHCHO, CAS# 14189-82-3)

References

  1. ^ a b c "3-(Dimethylamino)acrolein 927-63-9 | TCI Deutschland GmbH". www.tcichemicals.com (in German). Retrieved 2018-01-14.
  2. ^ a b Sigma-Aldrich Co., product no. 305839.
  3. ^ a b c d DE 944852, F. Wille, "Verfahren zur Herstellung von Derivaten des 3-Amino-acroleins", published 1956-06-28, assigned to Badische Anilin- & Soda-Fabrik AG 
  4. ^ a b c DE 2424373, M. Decker, W. Schönleben, H. Toussaint, H. Hoffmann, "Verfahren zur Herstellung von Derivaten des Malondialdehyds", published 1975-12-11, assigned to BASF AG 
  5. ^ US 5780622, D. Dolphin, R. Boyle, "Methods of synthesizing 5,15-diarylbenzochlorine-7-one", published 1998-07-14, assigned to The University of British Columbia 
  6. ^ L.J. Niederhofer; J.S. Daniels; C.A. Rouzer; R.E. Greene; L.J. Marnett (2003), "Malondialdehyde, a product of lipid peroxidation, is mutagenic in human cells", J. Biol. Chem., vol. 278, no. 33, pp. 31426–31433, doi:10.1074/jbc.M212549200, PMID 12775726
  7. ^ a b D. Lloyd; H. McNab (1976), "Vinamidine and Vinamidinium-Salze – Beispiele für stabilisierte Push-Pull-Alkene", Angew. Chem., vol. 88, no. 15, pp. 496–504, doi:10.1002/ange.19760881503
  8. ^ S. Makhseed; H.M.E. Hassaneen; M.H. Elnagdi (2007), "Studies with 2-(Arylhydrazono)aldehydes: Synthesis and Chemical Reactivity of Mesoxalaldehyde 2-Arylhydrazones and of Ethyl 2-Arylhydrazono-3-oxopropionates" (PDF), Z. Naturforsch., vol. 62b, pp. 529–536
  9. ^ P. Perlmutter (2001), "Propargyl Aldehyde", E-EROS Encyclopedia of Reagents for Organic Synthesis, doi:10.1002/047084289X.rp262m, ISBN 0471936235
  10. ^ Z. Arnold; F. Sorm (1958), "Synthetische Reaktionen von Dimethylformamid. I. Allgemeine Synthese von β-Dialdehyden", Collect. Czech. Chem. Commun. (in German), vol. 23, no. 3, pp. 452–461, doi:10.1135/cccc19580452
  11. ^ DE 19825200, D. Golsch, M. Keil, H. Isak, "Verfahren zur Herstellung von 3-Aminoacroleinderivaten", published 1999-11-18, assigned to BASF AG 
  12. ^ H. Bredereck; F. Effenberger; G. Simchen (1963), "Säureamid-Reaktionen, XXXII. Über Säureamid-Dialkylsulfat-Komplexe", Chem. Ber. (in German), vol. 96, no. 5, pp. 1350–1355, doi:10.1002/cber.19630960526
  13. ^ H. Bredereck; F. Effenberger; D. Zeyfang (1965), "Synthese und Reaktionen vinyloger Amidacetale und Amidine", Angew. Chem. (in German), vol. 77, no. 5, p. 219, Bibcode:1965AngCh..77..219B, doi:10.1002/ange.19650770511
  14. ^ C. Jutz; C. Jutz; R.M. Wagner (1972), "Die synchrone Sechs-Elektronen-Cyclisierung von Hexatrien-Systemen als neues Syntheseprinzip zur Darstellung von Aromaten und Heteroaromaten", Angew. Chem. (in German), vol. 84, no. 7, pp. 299–302, Bibcode:1972AngCh..84..299J, doi:10.1002/ange.19720840714
  15. ^ F.W. Ulrich; E. Breitmeier (1983), "Vinyloge Vilsmeier-Formylierung mit 3-(N,N-Dimethylamino)-acroleinen", Synthesis (in German), vol. 1983, no. 8, pp. 641–645, doi:10.1055/s-1983-30457, S2CID 95436195
  16. ^ D. Sriram; P. Yogeeswari (2010), Medicinal Chemistry (2nd ed.), Delhi: Pearson, p. 364, ISBN 978-81-317-3144-4
  17. ^ J.T. Zacharia; T. Tanaka; M. Hagashi (2010), "Facile and highly enenatioselective synthesis of (+)- and (−)-fluvastatin and their analogues", J. Org. Chem., vol. 75, no. 22, pp. 7514–7518, doi:10.1021/jo101542y, PMID 20939538
  18. ^ EP 0731094, H.-J. Wroblowsky, R. Lantzsch, "Verfahren zur Herstellung von Pyrazolen", published 1996-09-11, assigned to Bayer AG 
  19. ^ Z. Arnold; J. Zemlicka (1960), "Reaktionen der Formamidinium-salze und ihrer Vinyloge mit Carbanionen", Collect. Czech. Chem. Commun. (in German), vol. 25, no. 5, pp. 1302–1307, doi:10.1135/cccc19601302
  20. ^ V. Nair; C.S. Cooper (1981), "Chemistry of 1,5-diazapentadienium (vinamidinium) salts: alkylation reactions to multifunctional dienamines and dienaminones", J. Org. Chem., vol. 46, no. 23, pp. 4759–4765, doi:10.1021/jo00336a027
  21. ^ Z. Arnold; D. Dvorak; M. Havranek (1996), "Convenient preparation of 1,3-Bis(dimethylamino)trimethinium perchlorate, tetrafluoroborate and hexafluorophosphate", Collect. Czech. Chem. Commun., vol. 61, no. 11, pp. 1637–1641, doi:10.1135/cccc19961637
  22. ^ V. Nair; C.S. Cooper (1980), "Selective alkylation reactions with vinamidinium salts", Tetrahedron Lett., vol. 21, no. 33, pp. 3155–3158, doi:10.1016/S0040-4039(00)77433-8
  23. ^ M.T. Wright; D.G. Carroll; T.M. Smith; S.Q. Smith (2010), "Synthesis of alkylpyrroles by use of a vinamidinium salt", Tetrahedron Lett., vol. 51, no. 31, pp. 4150–4152, doi:10.1016/j.tetlet.2010.06.009
  24. ^ R.T. Clemens; S.Q. Smith (2005), "The application of vinamidinium salts to the synthesis of 2,4-disubstituted thiophenes", Tetrahedron Lett., vol. 46, no. 8, pp. 1319–1320, doi:10.1016/j.tetlet.2004.12.113
  25. ^ EP 0372654, L. Schröder, "Preparation of 2-chloropyridine 3-carboxylic acid esters", published 1990-06-13, assigned to Shell Internationale Research Maatschappij B.V. 
  26. ^ WO 0007989, D. Golsch, M. Keil, H. Isak, H. Mayer, "Verfahren zur Herstellung von 2-Halogennikotinsäurederivaten und 2-Halogennikotinsäure-n-butylester als Zwischenprodukt", published 2000-02-17, assigned to BASF AG 
  27. ^ Randolph P. Thummel (2001). "(Z)-β-Aminoacrolein". e-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.ra087. ISBN 0471936235.
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