A Mild Synthesis of New Aryl Vinyl Ethers and Diethyl 1-[(Alkyl)(cyano)methyl]vinylphosphonates via the Substitution of a 2,3-Difunctional Allyl Bromide

Fray, Asma; Ben Kraïem, Jihène; Arfaoui, Aïcha; Amri, Hassen

doi:https://doi.org/10.1155/2014/260325

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Research Article | Open Access

Volume 2014 | Article ID 260325 | https://doi.org/10.1155/2014/260325

A Mild Synthesis of New Aryl Vinyl Ethers and Diethyl 1-[(Alkyl)(cyano)methyl]vinylphosphonates via the Substitution of a 2,3-Difunctional Allyl Bromide

Asma Fray,¹Jihène Ben Kraïem,²Aïcha Arfaoui,¹and Hassen Amri¹

Academic Editor: T. Mino, H. Miyabe

Received13 Dec 2013

Accepted02 Jan 2014

Published12 Feb 2014

Abstract

A novel class of aryl vinyl ethers 3 and diethyl 3-cyano-3-alkylprop-1-en-2-ylphosphonates 4 has been prepared, respectively, from coupling reaction of diethyl 1-(bromomethyl)-2-cyanovinylphosphonate 2 with phenols and Gilman reagents.

1. Introduction

The development of new strategies for the synthesis of organic compounds containing an α-bromomethyl group as in product 1 continues to pose a challenge to organic chemists. It has resulted in a wide variety of applications in the preparation of several natural [1–4] as well as biologically active compounds [5–8]. Moreover, the utility of these versatile allyl brominated intermediates 1 [9–18] comes from their reaction with different nucleophilic species and additionally their ability to act as excellent Michael acceptors. Because of its importance, it is still of interest to develop novel approaches for the efficient generation of functionalized allyl bromide 1. In this regard, we have previously described a simple and stereoselective synthesis of diethyl (E)-1-(bromomethyl)-2-cyanovinylphosphonate 2 [19], an activated alkene bearing three functional groups. We have also demonstrated that the latter can be used as an efficient electrophilic synthon for the synthesis of a new family of allylamines [19], enamines [20], and vinyl ether [20]. Prompted by the versatility of allyl bromide 2, we suggested that its reaction with a variety of phenols and Gilman reagents would be a very convenient way to prepare new substituted aryl vinyl ethers 3 and diethyl 1-[(alkyl)(cyano)methyl]vinylphosphonates 4 (Scheme 1).

2. Results and Discussion

Functional aryl vinyl ethers have been shown to be promising building blocks in organic synthesis [21–23] as well as important intermediates for the synthesis of a range of products [24–33], new polymeric materials [34–36], and biologically active molecules [37]. Thus, the preparation of these kinds of molecules has always attracted the attention of organic chemists and a growing effort has been directed toward the development of new vinyl ether-based structures and new methods for their construction [38–49]. Examination of the synthetic approaches to a wide variety of vinyl ethers has shown serious limitations, such as the use of strong acids or bases, toxic metals, and high temperatures. Therefore, the need to implement new inexpensive and easy methodologies to produce functional vinyl ethers remains attractive. In this context, we expected that the substitution of the bromine atom in molecule 2 by aromatic alcohols as nucleophilic reagents might lead to the desired aryl vinyl ethers 3. Hence, condensation of allyl bromide 2 with phenol (1.0 equiv.) in the presence of potassium carbonate (1.2 equiv.) and in refluxing acetonitrile afforded the corresponding aryl vinyl ether 3a in 92% yield after 15 min. In order to generalize the reaction of allyl bromide 2 with various aromatic alcohols, we examined a variety of electronically and sterically substituted phenols. As shown in Table 1, the reaction proceeded smoothly regardless of the steric and electronic properties of these different phenols. With few exceptions, the reaction was generally carried out in 15 minutes in good to excellent yields (Scheme 2, Table 1).

The formation of vinyl ethers 3a–f is the result of the substitution of allyl bromide 2 by different aryloxy groups followed by isomerization. A plausible reaction pathway for the synthesis of these new trisubstituted alkenes 3a–f is shown in Scheme 3.

The structures of 3a–f were established on the basis of their ¹H and ¹³C NMR spectra and by heteronuclear multiple bond correlation (HMBC). Their stereochemistry has been assigned on the basis of NOESY experiment. A sample of 3a shows no correlation between the vinylic proton (δ: 7.53 ppm) and those of CH₂CN (δ: 3.34 ppm). This result indicates that the vinylic proton and the CH₂ group are on opposite sides of the double bond and therefore the alkene in 3a is E configuration.

This result allowed the consideration of other experimental goals to exploit the electrophilicity of allyl bromide 2 by examining its reactivity with other nucleophilic reagents such as organocuprates. Gilman reagents have been widely used for the construction of organic molecules [50–53], since their discovery in 1900. They display an excellent reactivity towards a wide range of electrophiles and readily undergo transmetallation to provide a variety of organometallic species as organocopper derivatives which react well with soft electrophiles and display excellent chemoselectivity [54]. As a follow-up of our research in the direct substitution of functionalized allyl bromide by organocuprates reagents [55], diethyl (E)-1-(bromomethyl)-2-cyanovinylphosphonate 2 constituted the ideal intermediate for the synthesis of new 2-cyanoethylphosphonates 4. As shown in Scheme 4, conjugate addition of dialkyl organocuprates, generated in situ at low temperature from Grignard reagents in the presence of LiCuBr₂, leads to the corresponding Michael acceptors 4 in an substitution process. The new vinylphosphonates 4 obtained are summarized in Table 2.

3. Conclusion

In summary, a practical and efficient synthesis of new substituted aryl vinyl ethers 3 and diethyl 1-[(alkyl)(cyano)methyl]vinylphosphonates 4 has been developed. The application of diethyl (E)-1-(bromomethyl)-2-cyanovinylphosphonate 2 in other processes will be communicated in due course.

4. Experimental Section

4.1. Materials and Instrumentation

Starting materials and solvents were purchased and used without further purification. ¹H-NMR and ¹³C-NMR spectra were recorded on a Bruker AMX 300 spectrometer working at 300 MHz, 121 MHz, and 75 MHz, respectively, for ¹H, ³¹P, and ¹³C with CDCl₃ as the solvent and TMS as the internal standard. The chemical shifts (δ) and coupling constants (J) are, respectively, expressed in parts per million (ppm) and hertz (Hz). All NMR spectra were acquired at 25°C. Assignments of proton (¹H-NMR) and carbon (¹³C-NMR) signals were secured by DEPT 135 and HMBC experiments. Multiplicity of peaks is indicated by the following: s, singlet; d, doublet; dd, doublet of doublets; t, triplet; dt, doublet of triplets; q, quartet; dq, doublet of quartets; hept, heptuplet; m, multiplet. All reactions were monitored by TLC on silica gel plates (Fluka Kieselgel 60 F254, Merck) eluting with the solvents indicated and visualized by a 254 nm UV lamp and aqueous potassium permanganate solution. For column chromatography, Fluka Kieselgel 70–230 mesh was used. The compounds were examined by gas chromatography-mass spectrometry (GC/MS) and spectra were recorded on an Agilent Technologies 6890 N instrument with an Agilent 5973 N mass detector (EI) and an HP5-MS 30 m × 0.25 mm capillary apolar column (stationary phase: 5% diphenyldimethylpolysiloxane film, 0.25 μm). rt indicates the retention time. IR spectra were recorded on a Bruker Vertex 70 FT-IR spectrophotometer. The elementary analyses (C, H, and N) were performed on a Perkin-Elmer Series II CHNS/O Analyzer 2400.

4.2. General Procedure for the Synthesis of Aryl Vinyl Ethers (3a–f)

A mixture of allyl bromide (E)-1 (282 mg, 1.0 mmol), phenol (1.0 mmol), and powdered anhydrous K₂CO₃ (165 mg, 1.2 mmol) in acetonitrile (3 mL) was refluxed for 15 to 45 minutes under a nitrogen atmosphere with stirring. The reaction mixture was allowed to cool and evaporated to dryness, and the residue was extracted with ethyl acetate (3 × 20 mL) and then the organic layer was washed with brine (20 mL), dried over MgSO₄, and concentrated under reduced pressure. The obtained liquid was purified by column chromatography (Hexane-AcOEt, 1 : 1).

4.2.1. Diethyl (E)-[1-Cyanomethyl-2-(phenoxy)]vinylphosphonate (3a)

Yellow liquid. Yield: 92%, IR (neat): 3011, 2225, 1713, 1455, 1242 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 7.53 (d, 1H, ³J_HP = 12 Hz, =CH); 7.38 (t, 2H, J = 9 Hz, aromatic H); 7.20 (t, 1H, J = 9 Hz, aromatic H); 7.09 (d, 2H, J = 9 Hz, aromatic H); 4.15 (dq, J = 7.5 Hz, J = 7.5 Hz, 4H, 2OCH₂); 3.34 (d, 2H, ³J_HP = 15 Hz, CH₂); 1.38 (t, 6H, J = 7.5 Hz, 2CH₃); ¹³C-NMR (75 MHz, CDCl₃): 157.0 (d, =CH, ²J_CP = 27.75 Hz); 156.1 (aromatic C); 130.0 (aromatic CH); 125.2 (aromatic CH); 117.6 (aromatic CH); 116.6 (d, CN, ³J_CP = 3.75 Hz); 98.4 (d, =C, ¹J_CP = 201 Hz); 62.3 (d, 2OCH₂, ²J_CP = 5.25 Hz); 16.2 (d, 2CH₃, ³J_CP = 6.75 Hz); 12.9 (d, CH₂, ²J_CP = 6 Hz); ³¹P-NMR (121 MHz, CDCl₃): 17.70; GC/MS (EI): rt = 32.21 min, m/z = 295 (M+, 54), 239 (58), 94 (100), 77 (78), 65 (55) 51 (36). Anal. calcd for C₁₄H₁₈NO₄P (295,10): C, 56.95; H, 6.14; N, 4.74. Found: C, 56.67; H, 5.04; N, 4.03.

4.2.2. Diethyl (E)-[1-Cyanomethyl-2-(4-methylphenoxy)]vinylphosphonate (3b)

Yellow liquid. Yield: 68%, IR (neat): 3015, 2222, 1715, 1456, 1245 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 7.49 (d, 1H, ³J_HP = 12 Hz, =CH); 7.15 (d, 2H, J = 9 Hz, aromatic H); 6.98 (d, 2H, J = 9 Hz, aromatic H); 4.15 (dq, 4H, J = 7.5 Hz, 4H, J = 7.5 Hz, 2OCH₂); 3.33 (d, 2H, ³J_HP = 15 Hz, CH₂); 2.33 (s, 3H, CH₃); 1.38 (t, 6H, J = 7.5 Hz, 2CH₃); ¹³C-NMR (75 MHz, CDCl₃): 157.5 (d, =CH, ²J_CP = 27.75 Hz); 154.1 (aromatic C); 134.9 (aromatic C); 130.4 (aromatic CH); 117.2 (aromatic CH); 116.7 (d, CN, ³J_CP = 3.75 Hz); 97.8 (d, =C, ¹J_CP = 201 Hz); 62.8 (d, 2OCH₂, ²J_CP = 6 Hz); 20.7 (s, CH₃); 16.3 (d, 2CH₃, ³J_CP = 6 Hz); 12.9 (d, CH₂, ²J_CP = 6 Hz); ³¹P-NMR (121 MHz, CDCl₃): 17.91; GC/MS (EI): rt = 37.9 min, m/z = 309 (M+, 40), 202 (36), 146 (33), 108 (100), 91 (44), 77 (33), 65 (38). Anal. calcd for C₁₅H₂₀NO₄P (309,11): C, 58.25; H, 6.52; N, 4.53. Found: C, 57.98; H, 5.62; N, 4.47.

4.2.3. Diethyl (E)-[1-Cyano-2-(3-hydroxyphenoxy)]vinylphosphonate (3c)

Yellow liquid. Yield: 84%, IR (neat): 3356, 3013, 2222, 1718, 1454, 1243 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 8.94 (br, s, 1H, OH); 7.62 (d, 1H, ³J_HP = 12 Hz, =CH); 7.13 (t, 1H, J = 7.5 Hz, aromatic H); 6.72 (s, 1H, aromatic H); 6.70 (d, 1H, J = 9 Hz, aromatic H); 6.56 (d, 1H, J = 9 Hz, aromatic H); 4.16 (dq, 4H, J = 7.5 Hz, J = 7.5 Hz, 2OCH₂); 3.33 (d, 2H, ³J_HP = 15 Hz, CH₂); 1.39 (t, 6H, J = 7.5 Hz, 2CH₃); ¹³C-NMR (75 MHz, CDCl₃): 158.5 (aromatic C); 157.7 (d, =CH, ²J_CP = 29.25 Hz); 156.9 (aromatic C); 130.4 (aromatic CH); 116.6 (d, CN, ³J_CP = 3.75 Hz); 112.3 (aromatic CH); 108.6 (aromatic CH); 104.4 (aromatic CH); 96.8 (d, =C, ¹J_CP = 203.25 Hz); 62.8 (d, 2OCH₂, ²J_CP = 5.25 Hz); 16.2 (d, 2CH₃, ³J_CP = 6.75 Hz); 12.8 (CH₂, ²J_CP = 6 Hz); ³¹P-NMR (121 MHz, CDCl₃): 18.83; GC/MS (EI): rt = 38.93 min, m/z = 311 (M+, 52), 146 (30), 110 (100), 81 (35), 65 (36). Anal. calcd for C₁₄H₁₈NO₅P (311,09): C, 54.02; H, 5.83; N, 4.50. Found: C, 53.81; H, 5.75; N, 4.45.

4.2.4. Diethyl (E)-[1-Cyanomethyl-2-(4-nitrophenoxy)]vinylphosphonate (3d)

Orange liquid. Yield: 88%, IR (neat): 3012, 2220, 1721, 1538, 1456, 1235 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 8.29 (d, 2H, J = 9 Hz, aromatic H); 7.61 (d, 1H, ³J_HP = 12 Hz, =CH); 7.28 (d, 2H, J = 9 Hz, aromatic H); 4.19 (dq, 4H, J = 7.5 Hz, 4H, J = 7.5 Hz, 2OCH₂); 3.39 (d, 2H, ³J_HP = 15 Hz, CH₂); 1.40 (t, 6H, J = 7.5 Hz, 2CH₃); ¹³C-NMR (75 MHz, CDCl₃): 159.8 (aromatic C); 154.2 (d, =CH, ²J_CP = 27.75 Hz); 144.7 (aromatic C); 126.1 (aromatic CH); 117.5 (aromatic CH); 116.1 (d, CN, ³J_CP = 3.75 Hz); 102.2 (d, =C, ¹J_CP = 198 Hz); 62.8 (d, 2OCH₂, ²J_CP = 6 Hz); 16.3 (d, 2CH₃, ³J_CP = 6.75 Hz); 13.1 (d, CH₂, ²J_CP = 6 Hz); ³¹P-NMR (121 MHz, CDCl₃): 16.17; GC/MS (EI): rt = 44.43 min, m/z = 340 (M+, 38), 295 (50), 267 (100), 146 (29), 109 (27), 81 (44), 66 (34). Anal. calcd for C₁₄H₁₇N₂O₆P (340,08): C, 49.42; H, 5.04; N, 8.23. Found: C, 49.20; H, 4.97; N, 8.13.

4.2.5. Diethyl (E)-[1-Cyanomethyl-2-(3-methoxyphenoxy)]vinylphosphonate (3e)

Yellow liquid. Yield: 78%, IR (neat): 3012, 2220, 1720, 1452, 1248, 1037 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 7.52 (d, 1H, ³J_HP = 12 Hz, =CH); 7.26 (t, 1H, J = 7.5 Hz, aromatic H); 6.74 (d, 1H, J = 9 Hz, aromatic H); 6.68 (d, 1H, J = 9 Hz, aromatic H); 6.64 (s, 1H, aromatic H); 4.16 (dq, 4H, J = 7.5 Hz, J = 7.5 Hz, 2OCH₂); 3.81 (s, 3H, OCH₃); 3.33 (d, 2H, ³J_HP = 15 Hz, CH₂); 1.39 (t, 6H, J = 7.5 Hz, 2CH₃); ¹³C-NMR (75 MHz, CDCl₃): 161.0 (aromatic C); 157.0 (aromatic C); 156.9 (d, =CH, ²J_CP = 27.75 Hz); 130.5 (aromatic CH); 116.6 (d, CN, ³J_CP = 3.75 Hz); 111.0 (aromatic CH); 109.3 (aromatic CH); 103.7 (aromatic CH); 98.4 (d, =C, ¹J_CP = 200.25 Hz); 62.3 (d, 2OCH₂, ²J_CP = 5.25 Hz); 55.5 (OCH₃); 16.2 (d, 2CH₃, ³J_CP = 6 Hz); 12.9 (d, CH₂, ²J_CP = 6 Hz); ³¹P-NMR (121 MHz, CDCl₃): 17.64. Anal. calcd for C₁₅H₂₀NO₅P (325,11): C, 55.38; H, 6.20; N, 4.31. Found: C, 55.14; H, 6.14; N, 4.35.

4.2.6. Diethyl (E)-[1-Cyanomethyl-2-(2,4,6-tribromophenoxy)]vinylphosphonate (3f)

White solid. Yield: 57%, IR (neat): 3010, 2220, 1712, 1455, 1241 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 7.73 (s, 2H, aromatic H); 7.01 (d, 1H, ³J_HP = 12 Hz, =CH); 4.14 (dq, 4H, J = 7.5 Hz, 4H, J = 7.5 Hz, 2OCH₂); 3.40 (d, 2H, ³J_HP = 15 Hz, CH₂); 1.39 (t, 6H, J = 7.5 Hz, 2CH₃); ¹³C-NMR (75 MHz, CDCl₃): 157.5 (d, =CH, ²J_CP = 28.5 Hz); 149.9 (aromatic C); 135.3 (aromatic CH); 120.3 (aromatic C); 117.7 (aromatic C); 116.1 (d, CN, ³J_CP = 3.75 Hz); 100.0 (d, =C, ¹J_CP = 198 Hz); 62.5 (d, 2OCH₂, ²J_CP = 5.25 Hz); 16.2 (d, 2CH₃, ³J_CP = 7.5 Hz); 12.9 (d, CH₂, ²J_CP = 5.25 Hz); ³¹P-NMR (121 MHz, CDCl₃): 16.35; GC/MS (EI): rt = 43.34 min, m/z = 531 (M+, 8), 452 (44), 396 (100), 369 (38), 330 (22), 146 (52), 81 (72), 66 (42). Anal. calcd for C₁₄H₁₅Br₃NO₄P (528,83): C, 31.61; H, 2.84; N, 2.63. Found: C, 31.57; H, 2.72; N, 2.59.

4.3. Representative Synthetic Procedure of Diethyl 1-[(Alkyl)(cyano)methyl]vinylphosphonates (4a–d)

To a mixture of diethyl (E)-1-bromomethyl-2-cyanovinylphsphonate 1 (1.25 g, 5 mmol) and 1 M solution of LiCuBr₂ (0.15 mL, 3 mol %) in dry THF (20 mL) was added dropwise a solution of alkylmagnesium halide (RMgX) at (−78°C) under a nitrogen atmosphere. The resulting mixture was stirred for a few minutes and then quenched with saturated NH₄Cl solution (10 mL) and extracted with ether (3 × 20 mL). The combined organic layers were dried over MgSO₄, filtered, and evaporated under reduced pressure. The crude product was purified by flash chromatography on silica gel (Et₂O/hexane, 9 : 1) to afford diethyl 1-[(alkyl)(cyano) methyl]vinylphosphonates 4a–d.

4.3.1. Diethyl 3-Cyanopent-1-en-2-ylphosphonate (4a)

Yellow Liquid. Yield: 74%. IR (neat): 2226, 1689, 1242 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 6.30 (d, 1H, ³J_HP = 21 Hz, =CH); 6.22 (d, 1H, ³J_HP = 45 Hz, =CH); 4.12 (dq, 4H, J = 7.5 Hz, J = 7.5 Hz, 2OCH₂); 3.56 (dt, 1H, ³J_HP = 9 Hz, J = 6 Hz, CH); 2.00–1.77 (m, 2H, CH₂); 1.35 (2t, 6H, J = 7.5 Hz, J = 7.5 Hz, 2CH₃); 1.09 (t, 3H, J = 7.5 Hz, CH₃); ¹³C-NMR (75 MHz, CDCl₃): 137.1 (d, =C, ¹J_CP = 181.3 Hz); 132.1 (d, =CH₂, ²J_CP = 8.25 Hz); 116.9 (d, CN, ³J_CP = 14.25 Hz); 62.4 (d, 2OCH₂, ²J_CP = 6 Hz); 35.9 (d, CH, ²J_CP = 16.5 Hz); 25.9 (d, CH₂, ³J_CP = 2.25 Hz); 16.1 (d, 2CH₃, ³J_CP = 6 Hz); 10.9 (CH₃); ³¹P-NMR (121 MHz, CDCl₃): 15.54; GC/MS (EI): rt = 42.81 min, m/z = 231 (M+, 3), 167 (29), 149 (100), 71 (19), 57 (34). Anal. calcd for C₁₀H₁₈NO₃P (231,10): C, 51.94; H, 7.85; N, 6.06. Found: C, 51.69; H, 7.83; N, 6.03.

4.3.2. Diethyl 3-Cyano-4-methylpent-1-en-2-ylphosphonate (4b)

Yellow Liquid. Yield: 92%. IR (neat): 2224, 1696, 1243 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 6.31 (d, 1H, ³J_HP = 21 Hz, =CH); 6.20 (d, 1H, ³J_HP = 45 Hz, =CH); 4.12 (dq, 4H, J = 7.5 Hz, J = 7.5 Hz, 2OCH₂); 3.57 (dd, 1H, ³J_HP = 12 Hz, J = 6 Hz, CH); 2.28 (hept, 1H, J = 6 Hz, CH); 1.34 (t, 6H, J = 6 Hz, 2CH₃); 1.14 (d, 3H, J = 6 Hz, CH₃); 0.98 (d, 3H, J = 6 Hz, CH₃); ¹³C-NMR (75 MHz, CDCl₃): 134.1 (d, =C, ¹J_CP = 176.25 Hz); 132.9 (d, =CH₂, ²J_CP = 7.5 Hz); 117.7 (d, CN, ³J_CP = 15.75 Hz); 62.5 (d, 2OCH₂, ²J_CP = 12.75 Hz); 42.4 (d, CH, ²J_CP = 17.25 Hz); 29.4 (³J_CP = 1.5 Hz, CH); 21.5 (CH₃); 16.3 (d, 2CH₃, ³J_CP = 6 Hz); ³¹P-NMR (121 MHz, CDCl₃): 15.63; GC/MS (EI): rt = 24.16 min, m/z = 244 (M-1, 3), 203 (33), 175 (24), 147 (100), 81 (11), 66 (24). Anal. calcd for C₁₁H₂₀NO₃P (245,12): C, 53.87; H, 8.22; N, 5.71. Found: C, 53.54; H, 7.48; N, 5.79.

4.3.3. Diethyl 3-Cyano-5-methylhex-1-en-2-ylphosphonate (4c)

Colorless liquid. Yield: 88%. IR (neat): 2226, 1693, 1244 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 6.3 (d, 1H, ³J_HP = 24 Hz, =CH); 6.23 (dd, 1H, ³J_HP = 45 Hz, J = 3 Hz, =CH); 4.12 (dq, 4H, J = 7.5 Hz, J = 7.5 Hz, 2OCH₂); 3.56 (dt, 1H, ³J_HP = 9 Hz, J = 6 Hz, CH); 1.60 (hept, 1H, J = 6 Hz,CH); 1.40-1.26 (m, 2H, CH₂); 1.35 (2t, 6H, J = 7.5 Hz, J = 7.5 Hz, 2CH₃); 0.92 (2d, 6H, J = 6 Hz, 2CH₃); ¹³C-NMR (75 MHz, CDCl₃): 134.8 (d, =C, ¹J_CP = 181.5 Hz); 132.5 (d, =CH₂, ²J_CP = 8.25 Hz); 119.3 (d, CN, ³J_CP = 13.5 Hz); 62.5 (d, 2OCH₂, ²J_CP = 8.25 Hz); 35.7 (d, CH₂, ³J_CP = 1.5 Hz, CH₂); 34.5 (d, CH, ²J_CP = 16.5 Hz); 27.5 (CH); 22.5 (CH₃); 22.1 (CH₃); 16.2 (d, 2CH₃, ³J_CP = 6.75 Hz); ³¹P-NMR (121 MHz, CDCl₃): 15.65; GC/MS (EI): rt = 28.04 min, m/z = 272 (M-1, 5), 233 (43), 203 (32), 174 (30), 160 (19), 147 (100), 138 (27), 66 (36). Anal. calcd for C₁₃H₂₄NO₃P (259,28): C, 55.59; H, 8.55; N, 5.40. Found: C, 56.44; H, 8.43; N, 5.35.

4.3.4. Diethyl 3-Cyano-4-(trimethylsilyl)but-1-en-2-ylphosphonate (4d)

Yellow liquid. Yield: 78%. IR (neat): 2223, 1711, 1242 cm⁻¹. ¹H-NMR (300 MHz, CDCl₃): 6.10 (dd, 1H, ³J_HP = 48 Hz, J = 3 Hz =CH); 6.08 (d, 1H, ³J_HP = 21 Hz, =CH); 3.97 (dq, 4H, J = 7.5 Hz, J = 7.5 Hz, 2OCH₂); 3.56 (m, 1H, CH); 1.96-1.8 (2 m, 2H, CH₂); 1.20 (2t, 6H, J = 6 Hz, J = 6 Hz, 2CH₃); 0.00 (s, 9H, SiMe₃); ¹³C-NMR (75 MHz, CDCl₃): 139.2 (d, =C, ¹J_CP = 180 Hz); 132.6 (d, =CH₂, ²J_CP = 8.25 Hz); 121.8 (d, CN, ³J_CP = 12 Hz); 62.5 (d, 2OCH₂, ²J_CP = 9 Hz); 29.4 (d, CH, ²J_CP = 15.75 Hz); 21.4 (d, CH₂, ³J_CP = 2.25 Hz); 16.2 (d, 2CH₃, ³J_CP = 6.75 Hz); −1.57 (s, SiMe₃); ³¹P-NMR (121 MHz, CDCl₃): 15.69. Anal. calcd for C₁₂H₂₄NO₃PSi (289,13): C, 49.81; H, 8.36; N, 4.84. Found: C, 49.60; H, 8.07; N, 4.76.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work was supported by the Higher Education and Scientific Research of Tunisia. The authors wish to thank Professors Jacques Lebreton (University of Nantes, France) and Adel Nefzi (University of California, San Diego) for logistical help.

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Copyright © 2014 Asma Fray et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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