Cobalt(II) chloride-mediated synthesis of beta-enamino compounds under solvent-free conditions

Abstracts

A variety of beta-enaminones and beta-enamino esters can be synthesized by the reaction of 1,3-dicarbonyl compounds with amines in the presence of a catalytic amount of cobalt(II) chloride at room temperature under solvent-free condition. The experiment procedure is simple, and the products are straightforwardly isolated in high yields.

beta-enaminones; beta-enamino esters; 1,3-dicarbonyl compounds; amines; cobalt(II) chloride; solvent-free conditions

Uma variedade de beta-enaminonas e beta-enamino ésteres foi sintetizada pela reação de compostos 1,3-dicarbonílicos com aminas na presença de quantidade catalítica de cloreto de cobalto(II), à temperatura ambiente na ausência de solventes. O procedimento experimental é simples e os produtos são isolados em altos rendimentos.

SHORT REPORT

Cobalt(II) chloride-mediated synthesis of b-enamino compounds under solvent-free conditions

Zhan-Hui Zhang^{*, I}; Jin-Yong Hu^II

^IThe College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050016, China

^IIDivision of Science and Technology, Hebei Normal University, Shijiazhuang 050016, China

ABSTRACT

A variety of b-enaminones and b-enamino esters can be synthesized by the reaction of 1,3-dicarbonyl compounds with amines in the presence of a catalytic amount of cobalt(II) chloride at room temperature under solvent-free condition. The experiment procedure is simple, and the products are straightforwardly isolated in high yields.

Keywords: b-enaminones, b-enamino esters, 1,3-dicarbonyl compounds, amines, cobalt(II) chloride, solvent-free conditions

RESUMO

Uma variedade de b-enaminonas e b-enamino ésteres foi sintetizada pela reação de compostos 1,3-dicarbonílicos com aminas na presença de quantidade catalítica de cloreto de cobalto(II), à temperatura ambiente na ausência de solventes. O procedimento experimental é simples e os produtos são isolados em altos rendimentos.

Introduction

b-Enaminones have attracted much attention due to the fact that they are important synthons for the synthesis of many biologically active compounds such as dopamine auto-receptor agonists,¹ acetylcholinestersase inhibitors² and anticonvulsants.³ They are also useful intermediates for the preparation of several aminoacids,⁴ aminols,⁵ peptides and alkaloids.⁶ Thus it is very important to search for a convenient and efficient method for the synthesis of this type of compounds.⁷ Several methods have been developed for their synthesis including the reactions of imidoyl chlorides with acetonyltributyltin in the presence of palladium catalyst,⁸ the addition of amines to acylacetylenes,⁹ acylation of metalated ketimines using acylbenzotriazoles as acylating agents,¹⁰ the reactions of lithiated enamines with diethyl carbonate or benzyl chloroformate,¹¹ the addition of ester or amide enolates to nitriles,¹² palladium-assisted amination of a-keto olefins⁹ or amination with O-methylhydroxylamines in the presence of base,¹³ and the reactions of alkyl azides and b-ketoesters in a one-pot procedure using 10% Pd/C catalyst and hydrogen.¹⁴ However, the most commonly used and straightforward approach for the preparation of these compounds is the direct condensation of b-dicarbonyl compounds and amines, in which the azeotropic removal of water is usually required under reflux using a Dean Stark trap in aromatic solvent.¹⁵ Some improved procedures have been also reported to utilize protonic acids such as HCl,¹⁶ H₂SO₄,¹⁷p-TSA,¹⁸ ultrasound/HAc,¹⁹ Lewis acids such as BF₃·OEt₂,²⁰ Zn(ClO₄)₂·6H₂ O,²¹ CeCl₃·7H₂O,²² NaAuCl₄,²³ Bi(OTf)₃²⁴ and heterogeneous catalyst like natural clays,²⁵ silica gel,²⁶ montmorillonite K10,²⁷ sulfated zirconia,²⁸ silica chloride²⁹ and microwaves/K-10.³⁰ Recently, I₂,³¹ InBr₃,³² Zn(OAc)₂·6H₂O,³³ [EtNH₃]NO₃,³⁴ Sc(OTf)₃³⁵ and HClO₄·SiO₂³⁶ have been employed to promote this reaction. This condensation reaction has also been performed in water.³⁷ However, there are always some drawbacks with these procedures such as long reaction time,^26,33 high temperature,¹⁵ use of costly catalysts,^23,24,35 high catalyst loading,^22,31 use of an additional ultrasound¹⁹ or microwave oven³⁰ etc. So, the development of new reagents with great efficiency, convenient procedure, and delivery of better yields is of great interest.

Recently, cobalt salts have been introduced as mild and extraordinarily efficient catalysts for various organic transformations.³⁸ Particularly, cobalt(II) chloride is easily availability, inexpensive, water tolerant and operates under nearly neutral conditions, its further exploration for other organic transformations will be quite useful. As a part of our ongoing program in developing various new synthetic transformations using cheap and eco-friendly materials as catalysts,³⁹ we herein wish to report our results on the synthesis of b-enaminones and b-enamino esters using a catalytic amount of CoCl₂·6H₂O at room temperature under solvent-free condition (Scheme 1).

Results and Discussion

Our initial studies were focused on the optimization of the reaction conditions for the synthesis of b-enamino esters. Ethyl acetoacetate was chosen as a model substrate for the optimization process. The reaction of ethyl acetoacetate with aniline in the presence of 5 mol% CoCl₂·6H₂O at room temperature, without any solvent, afforded the target ethyl 3-(phenylamino)but-2-enoate (3e) in 95% yield. Lower catalyst loading can be used with only a marginal drop in reaction rate. With the optimized reaction condition, we next studied the reactions of a series of b-ketoesters with amines. The results presented in Table 1 indicate the generality of the method and efficacy of CoCl₂·6H₂O as very mild catalyst. This method was successfully applied to enamination of simple linear b-ketoesters (a-j) and cyclic b-ketoesters (k-p). From the reaction of ethyl acetoacetate with various aryl amines, electronic effects were clearly observed. In general, aryl amines having no substituents or electron-donating substituents on the aromatic ring were more reactive, and afforded the corresponding products 3 in better yields (Table 1, 3e, 3g and 3h). An electron-withdrawing group had a strong deactivating effect, thus longer reaction time was required and the corresponding product was obtained in lower yield (Table 1, 2j). As expected, a steric interference was pronounced when the group is at the ortho-position of amine. In comparation to the synthesis of b-enamino esters 3e-3h, a decrease of the yield for the synthesis of 3i was observed. It is noteworthy that optically active amine was converted into the corresponding b-enamino ester without any racemization or inversion by measuring its optical rotation and comparing with the literature value (Table 1, 3d).

This method is equally effective for symmetrical and unsymmetrical b-diketones. In the case of unsymmetrical b-diketones, the regiochemistry was controlled by the more reactive carbonyl group, which underwent preferential attack of amine. For example, 1-benzoylacetone reacted with aniline to obtain exclusively single regioisomer 3x. When this reaction was conducted with symmetrical diamines, two equivalents of b-diketone were used to give the corresponding product with two enamino groups in high yields (Table 1, 3s). We also carried out the reaction of acetylacetone with equimolar amount of propane-1,3-diamine, but cyclic product was not obtained.

The method was found that the chemoselectivity was also very good. Amine attacked only at the ketone carbonyl for both diketones and b-ketoesters. The (Z)-selectivity in the products derived from acylic diketones and b-ketoesters was secured by intramolecular hydrogen bonding. The ¹H NMR spectra analyses of products supported this sterostructure, in which the proton of the –NH– group appeared in the region of 8.6-10.2 ppm.

The reaction proceeds very cleanly without the formation of any by-products except water. Because the reaction can be performed using a solvent-free procedure, at the end of the reaction, the crude mixture can be directly charge on a chromatographic column to obtain the pure product, avoiding any tedious work up.

In summary, we have developed a new and efficient procedure for the preparation of b-enamino compounds catalysed by CoCl₂·6H₂O. This method offers several advantages such as (i) short reaction times; (ii) no excess of the reactants and catalyst is demanded; (iii) no solvent is employed; (iv) cheap and commercially available catalyst is applied; (v) no work-up is need, since the crude mixture can be directly charged on a chromatography column for immediate purification, which leads to an useful and attractive process for the synthesis of this type of compounds simple by changing different substrates.

Experimental

Melting points were measured using a X-4 apparatus and are uncorrected. ¹H NMR spectra were taken with a Bruker 300 spectrometer in a CDCl₃ solution with tetramethylsilane as an internal standard. IR spectra were obtained using Bruker-TENSOR 27 spectrometer instrument. Mass spectra were recorded on a GC-MS Thermofinnigan Polaris-Q mass spectrometer. The elemental analyses were carried out in an Elemental Vario EL analyzer.

General procedure for the synthesis of b-enamino compounds

A mixture of 1,3-dicarbonyl compounds (5 mmol), amines (5 mmol) and CoCl₂·6H₂O (0.25 mmol, 58 mg) was stirred at room temperature for an appropriate time (see Table 1). After completion of the reaction, the crude products were separated by column chromatography on Et₃N pre-treated silica gel using petroleum ether (bp 60-80 ºC)/EtOAc (10:1) as eluent.

The spectral and analytical data of some representative compounds are given below.

(Z)-Methyl 3-(allylamino)but-2-enoate (3c) ⁴⁰

A yellowish oil; IR (neat) n_max/ cm^-1: 1655, 1606; ¹H NMR (CDCl₃, 300 MHz) d 1.91 (s, 3H), 3.64 (s, 3H), 3.82-3.86 (m, 2H), 4.99 (s, 1H), 5.15-5.26 (m, 2H), 5.83-5.94 (m, 1H), 8.66 (br s, 1H, NH); EIMS m/z (%): 155 (M⁺, 39), 140 (26), 96 (100), 79 (29); Anal. Calc. for C₈H₁₃NO₂: C, 61.91; H, 8.44; N, 9.03. Found: C, 62.12; H, 8.62; N, 8.88.

(Z)-methyl 3-((R)-1-phenylethylamino)but-2-enoate (3d)

A colorless liquid, [a]_D²⁰: - 550 (c 1.02, EtOH) [- 546]³²; IR (neat) n_max/ cm^-1: 1652, 1607; ¹H NMR (CDCl₃, 300 MHz) d 1.52 (d, J 6.9 Hz, 3H), 1.78 (s, 3H), 3.68 (s, 3H), 4.49 (s, 1H), 4.64 (q, J 6.9 Hz, 1H), 7.22-7.38 (m, 5H), 8.98 (br s, 1H, NH); EIMS m/z 219 (M⁺, 41), 204 (31), 172 (29), 145 (89), 105 (100), 84 (17); Anal. Calc. for C₁₃H₁₇NO₂: C, 71.21; H, 7.81; N, 6.39. Found: C, 61.48; H, 8.02; N, 6.18.

(Z)-Methyl 3-(o-tolylamino)but-2-enoate (3f)

A pale yellow solid, mp. 28-30 ºC [26-27 ºC]³²; IR (KBr) n_max/ cm^-1: 1648, 1598; ¹H NMR (CDCl₃, 300 MHz) d 1.85 (s, 3H), 2.28 (s, 3H), 3.68 (s, 3H), 4.70 (s, 1H), 7.02-7.23 (m, 4H), 10.12 (br s, 1H, NH); EIMS m/z 205 (M⁺, 44), 190 (11)), 174 (16), 158 (14), 146 (30), 132 (100), 117 (21); Anal. Calc. for C₁₂H₁₅NO₂: C, 70.22; H, 7.37; N, 6.82. Found: C, 69.98; H, 7.52; N, 6.68.

(Z)-Ethyl 3-(p-tolylamino)but-2-enoate (3g) ⁴¹

A yellow oil; IR (neat) n_max/ cm^-1: 1654, 1608; ¹H NMR (CDCl₃, 300 MHz) d 1.29 (t, J 7.2 Hz, 3H), 1.96 (s, 3H), 2.33 (s, 3H), 4.15 (q, J 7.2 Hz, 2H), 4.67 (s, 1H), 6.98 (d, J 8.4 Hz, 2H), 7.13 (d, J 8.4 Hz, 2H), 10.28 (br s, 1H, NH); EIMS m/z 219 (M⁺, 84), 14 (39), 146 (100), 132 (81), 91 (35); Anal. Calc. for C₁₃H₁₇NO₂: C, 71.21; H, 7.81; N, 6.39. Found: C, 71.46; H, 8.04; N, 6.16.

(Z)-Ethyl 3-(p-ethoxyphenylamino)but-2-enoate (3h)

A pale yellow solid, mp 55-56 ºC [53-54 ºC]³²; IR (KBr) n_max/ cm^-1: 1652, 1613 cm^-1; ¹H NMR (CDCl₃, 300 MHz) d 1.29 (t, J 7.2 Hz, 3H), 1.42 (t, J 7.2 Hz, 3H), 1.89 (s, 3H), 4.02 (q, J 7.2 Hz, 2H), 4.15 (q, J 7.2 Hz, 2H), 4.65 (s, 1H), 6.85 (d, J 8.7 Hz, 2H), 7.02 (d, J 8.7 Hz, 2H), 10.16 (br s, 1H, NH); EIMS m/z 249 (M⁺, 17), 203 (100), 174 (31), 147 (51), 118 (29), 91(9); Anal. Calc. for C₁₄H₁₉NO₃: C, 67.45; H, 7.68; N, 5.62. Found: C, 67.70; H, 7.42; N, 5.85.

(Z)-Methyl 3-(2,6-diethylphenylamino)but-2-enoate (3i)

A pale yellow solid, mp 27-28 ºC [26-27 ºC]³²; IR (KBr) n_max/ cm^-1: 1658, 1607; ¹H NMR (CDCl₃, 300 MHz) d 1.19 (t, J 7.8 Hz, 6H), 1.62 (s, 3H), 2.52 (q, J 7.8 Hz, 2H), 2.63 (q, J 7.8 Hz, 2H), 3.71 (s, 3H), 4.87 (s, 1H), 7.13 (d, J 7.8 Hz, 2H), 7.19-7.24 (m, 1H), 9.88 (br s, 1H, NH); EIMS m/z 247 (M⁺, 18), 174 (100), 146 (33); Anal. Calc. for C₁₅H₂₁NO₂: C, 72.84; H, 8.65; N, 5.66. Found: C, 73.02; H, 8.46; N, 5.83.

3-(1-(2-Methoxyphenylamino)ethylidene)-dihydrofuran -2(3H)-one (3m)

A pale yellow solid, mp 93-94 ºC; IR (KBr) n_max/cm^-1: 1676, 1635; ¹HNMR (CDCl₃, 300 MHz) d 1.90 (s, 3H), 2.88 (t, J 7.8 Hz, 2H), 3.78 (s, 3H), 4.34 (t, J 7.8 Hz, 2H), 6.85 (d, J 7.8 Hz, 1H), 6.98 (d, J 7.8 Hz, 1H), 9.76 (br s, 1H, NH); Anal. Calc. for C₁₃H₁₅NO₃: C, 66.94; H, 6.48; N, 6.00. Found: C, 66.79; H, 6.25; N, 6.20.

1,3-Bis-(2-acetyl-1-methylvinylamino)propane (3s)

A dark brown solid, mp 50-52 ºC [51 ºC]⁴²; IR (KBr) n_max/ cm^-1: 1608, 1570; ¹H NMR (CDCl₃, 300 MHz) d1.89 (t, J 6.3 Hz, 2H), 1.92 (s, 6H), 2.01 (s, 6H), 3.38 (q, J 6.3 Hz, 4H), 5.00 (s, 2H), 10.92 (br s, 1H, NH); Anal. Calc. For C₁₃H₂₂N₂O₂ : C, 65.51; H, 9.30; N, 11.75. Found: C, 65.69; H, 9.18; N, 11.85.

(Z)-4-(o-Tolylamino)pent-3-en-2-one (3u)

A pale yellow solid, mp 38-40 ºC [37-38 ºC]³²; IR (KBr) n_max/ cm^-1: 1595, 1560; ¹HNMR (CDCl₃, 300 MHz) d 1.88 (s, 3H), 2.12 (s, 3H), 2.29 (s, 3H), 5.21 (s, 1H), 7.07-7.25 (m, 4H), 12.36 (br s, 1H, NH); EIMS m/z 189 (M⁺, 44), 174 (100), 146 (63), 131 (44), 91 (11); Anal. Calc. for C₁₂H₁₅NO: C, 76.16; H, 7.99; N, 7.40. Found: C, 76.02; H, 8.25; N, 7.65.

(Z)-3-(4-Ethoxy-phenylamino)-1-phenyl-but-2-en-1-one (3y)

A yellow solid, mp 84-85 ºC; IR (KBr) n_max/ cm^-1: 1599, 1504; ¹H NMR (CDCl₃, 300 MHz) d 1.40 (t, J 6.9 Hz, 3H), 2.05 (s, 3H), 4.02 (q, J 6.9 Hz, 2H), 5.85 (s, 1H), 6.89 (d, J 9.0 Hz, 2H), 7.10 (d, J 8.7 Hz, 2H), 7.44-7.47 (m, 3H), 7.90-7.94 (m, 2H), 12.88 (br s, 1H, NH); Anal. Calc. for C₁₈H₁₉NO₂: C, 76.84; H, 6.81; N, 4.98. Found: C, 76.95; H, 6.76; N, 4.72.

Acknowledgments

We thank the Science Research Foundation of Hebei Normal University, Natural Science Foundation of Hebei Province (B2005000151) and the Natural Science Foundation of Hebei Education Department (2006318) for financial support.

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Received: June 22, 2006

Published on the web: November 7, 2006

Publication Dates

• Publication in this collection
  29 Jan 2007
• Date of issue
  Dec 2006

History

• Received
  22 June 2006
• Accepted
  07 Nov 2006