IJOCInternational Journal of Organic Chemistry2161-4687Scientific Research Publishing10.4236/ijoc.2016.62016IJOC-67739ArticlesBiomedical&Life Sciences Chemistry&Materials Science Reaction of Arylnitroso Derivatives: Synthesis of Arylimino 2,5-Dihydrofuran and Arylamino Fulvenes Derivatives StefaniaFusi1*DonatoDonati1FabioPonticelli1Dipartimento di Biotecnologie, Chimica e Farmacia, Università di Siena, Siena, Italy* E-mail:stefania.fusi@unisi.it(SF);19052016060214715516 April 2016accepted 25 June 28 June 2016© Copyright 2014 by authors and Scientific Research Publishing Inc. 2014This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/

Herein we report the reactivity of N-(2,4-dicyano-1,5-dimethyl-3-arylcyclopenta-2,4-dienyl)-2,2,2- trifluoroacetamides and N,N-dimethyl-4-nitrosoaniline which provide compounds derived from Ehrlich-Sachs condensation, dihydrofuran derivatives and fulvene derivatives by adjusting the reaction conditions.

Cyclopentadienes Nitrsoarenes Dihydrofuran Fulvenes1. Introduction

Densely functionalized cyclopentadienes 1 were recently prepared [1] and exploited as useful building blocks in synthetic chemistry. We have previously reported, in a preliminary account, the preparation of notable compounds using 1 as starter material. These syntheses involved the cycloaddition of 1 with a suitable reagent, followed by rearrangement (Figure 1) [2] . As an expansion of this study, we focused on arylnitroso derivatives as potential reagents for cyclopentadiene 1. Arylnitroso species were shown to give numerous reactions with unsaturated molecules, including cycloadditions and Aldol Michael [3] - [9] . In this context, the formation of 1,2- oxazines would be of wide importance, due to the possibility of further chemical elaboration of this structure to access important scaffolds [10] . Herein we report our studies on the reactivity of N-(2,4-dicyano-1,5-dimethyl- 3-phenylcyclopenta-2,4-dienyl)-2,2,2-trifluoroacetamide and p-NO2, 2,4-di-NO2, p-OMe phenyl derivatives in presence of nitrosobenzene or N,N-dimethyl-4-nitrosoaniline. This reaction is showed to give different products in dependence of the experimental conditions applied.

Synthetic target from cyclopentadiene 12. Experimental2.1. Chemicals and Instruments

General: Melting point was measured with a Kofler apparatus and was uncorrected. The 1H and 13C NMR spectra were recorded at 400.13 MHz and 100.13 MHz on a Bruker Advance DPX400. Chemical shifts are reported relative to tetramethylsilane at 0.00 ppm. ESI-MS spectra were recorded with a LCQ-DECA Thermo Finnigan instrument. TLC was performed on precoated 4 × 6.7 silica gel 60 F254 plates silica gel on aluminum (Aldrich) with detection by UV light. Column chromatography was carried out on Silica gel (E. Merck, 0.040 - 0.063 mm). Microwave irradiations were conducted using a CEM Discover Synthesis Unit. Elemental analyses were performed on a Perkin Elmer PE 2004 Elemental Analyzer.

2.2. General Method for the Preparation of Compounds 3a-d

A mixture of compounds 1a-d (0.1 mmol) and N,N-dimethyl-4-nitrosoaniline 2 (0.12 mmol) in CH2Cl2 (3 ml) was stirred at room temperature for a week or in Sovirel tube in bath oil at 60˚C for 7 h. Alternatively the same mixture was heated under MW irradiation, (150 W) for 90 minutes. The crude reaction was purified by column chromatography (ethyl acetate/petroleum ether 1/4).

2(5Z)-5-((4-dimethylamino) phenylimino)-2acetyl-2-dihydro-2-methyl-4-phenylfuran-3-carbonitrile (3a)

Red oil (40% yield) 1H-NMR (CDCl3): δ (ppm) 1.80 (s, 3H, Me), 2.29 (s, 3H, Me), 2.98 (s, 6H, NMe2), 6.70 (d, 2H, J = 8.8 Hz, Ph), 7.47 - 7.53 (m, 5H, Ph), 8.00 - 8.07 (m, 2H, Ph). 13C-NMR (CDCl3): δ (ppm) 21.52, 24.67, 40.43, 92.33, 110.15, 112.03, 113.18, 118.44, 127.16, 129.38, 129.46, 131.29, 133.40, 147.08, 149.05, 152.49, 203.25. MS (ESI): 360 (M+H+); Anal. Calcd for C22H21N3O2: C, 73.52; H, 5.89; N, 11.69; Found: C, 73.28; H, 5.90; N, 11.73.

2’ (5Z)-5-((4-dimethylamino) phenylimino)-2-acetyl-2,5-dihydro-2-methyl-4-(4’-nitrophenyl)furan-3-carbo ni- trile (3b)

Crystalline red solid (35% yield) (m.p. 146˚C - 147˚C) 1H-NMR (CDCl3): δ (ppm) 1.83 (s, 3H, Me), 2.33 (s, 3H, Me), 2.99 (s, 6H, NMe2), 6.69 (d, 2H, J = 9.0 Hz, Ph), 7.51 (d, 2H, J = 9.0 Hz, Ph), 8.20 (d, 2H, J = 8.8 Hz, Ph), 8.32 (d, 2H, J = 8.8 Hz, Ph). 13C-NMR (CDCl3): δ (ppm) 21.81, 24.90, 40.26, 92.82, 110.73, 111.04, 111.94, 123.56, 127.47, 130.62, 132.73, 134.03, 144.86, 148.90, 151.21, 151.62, 202.78. MS (ESI): 405 (M+H+); Anal. Calcd for C22H20N4O4: C, 63.34; H, 4.98; N, 13.85; Found: C, 63.55; H, 4.96; N, 13.89.

2’ (5Z)-5-((4-dimethylamino)phenylimino)-2-acetyl-2,5-dihydro-2-methyl-4-(2’-4’-nitrophenyl)furan-3-carbonitrile (3c)

Blu solid (20% yield) (m.p. 149˚C - 151˚C) 1H-NMR (CDCl3): δ (ppm) 1.97 (s, 3H, Me), 2.15 (s, 3H, Me), 3.08 (s, 6H, NMe2), 6.70 (d, 2H, J = 8.8 Hz, Ph), 7.36 (d, 2H, J = 8.8 Hz, Ph), 7.96 (d, 1H, J = 8.4 Hz, Ph), 8.67 (d, 1H, Jo = 8.4 Hz Jm = 1.6 Hz, Ph), 9.20 (bs, 1H). MS (ESI): 450 (M+H+); Anal. Calcd for C22H20N5O6: C, 58.80; H, 4.26; N, 15.58; Found: C, 59.00; H, 4.24; N, 21.43.

2’ (5Z)-5-((4-dimethylaminophenylimino)-2-acetyl-2,5-dihydro-2-methyl-4-(4’-methoxyphenyl)furan-3-carbonitrile (3d)

Crystalline orange-red solid (50% yield) (m.p. 148˚C - 150˚C) 1H-NMR (CDCl3): δ (ppm) 1.77 (s, 3H, Me), 2.26 (s, 3H, Me), 2.98 (s, 6H, NMe2), 3.86 (s, 3H, OMe), 6.69 (d, 2H, J = 8.8 Hz, Ph), 6.99 (d, 2H, J = 8.8 Hz, Ph), 7.49 (d, 2H, J = 8.8 Hz, Ph), 8.13 (d, 2H, J = 8.8 Hz, Ph). 13C-NMR (CDCl3): δ (ppm) 21.48, 24.58, 40.50, 55.45, 92.14, 112.15, 113.14, 114.08, 116.07, 120.64, 127.05, 131.33, 133.67, 146.13, 149.04, 153.01, 162.13, 203.34. MS (ESI): 390 (M+H+); Anal. Calcd for C23H23N3O3: C, 70.93; H, 5.95; N, 10.79; Found: C, 71.16; H, 5.93; N, 10.82.

2.3. General Method for the Preparation of Compounds 4a-d, 5a-d, 6a-d

Compounds 1a-d (0.1 mmol) and N,N-dimethyl-4-nitroso aniline 2 (0.12 mmol) were heated under MW irradiation at 150˚C for 15 minutes, 150 W solvent free or were heated in Sovirel tube in oil bath at 110˚C, solvent free for 3 h. The crude reaction was purified by column chromatography (ethyl acetate/petroleum ether 1/4).

(5Z)-5-((4-(dimethylamino)phenylamino)methylene)-4-methyl-2-phenylcyclopenta-1,3-diene-1,3-dicarbonitrile (4a)

Crystalline red solid (25% yield) m.p. 255˚C - 258˚C 1H-NMR (CDCl3): δ (ppm) 2.46 (s, 3H, Me), 2.99 (s, 6H, NMe2), 6.73 (d, 2H, J = 8.6 Hz, Ph), 7.13 (d, 2H, J = 8.6 Hz, Ph), 7.38 (d, 1H, J = 7.5 Hz, Ph), 7.45 (t, 2H, J = 7.5 Hz, Ph), 7.76 (d, 2H, J = 7.5 Hz, Ph), 7.89 (d, 1H, J = 15.0 Hz), 9.30 (d, 1H, J = 15.0 Hz, NH). 13C-NMR (CDCl3): δ (ppm) 11.85, 40.46, 101.51, 112.89, 115.89, 117.22, 119.44, 120.91, 126.96, 127.82, 128.86, 132.50, 142.61, 146.51, 147.34, 149.54. MS (ESI): 353 (M+H+); Anal. Calcd for C23H20N4: C, 78.38; H, 5.72; N, 15.90; Found: C, 78.63; H, 5.70; N, 15.86.

(Z)-N-((2,4-dicyano-5-methyl-3-phenyl-5-(2,2,2-trifluoroacetamido)cyclopenta-1,3-dien-1-yl)methylene)-4-(dimethylamino)aniline oxide (5a)

Red-violet solid (20% yield) m.p. 205˚C - 208˚C 1H-NMR (CDCl3): δ (ppm) 2.1 (s, 3H, Me), 3.07 (s, 6H, NMe2), 6.65 (d, 2H, J = 9.4 Hz, Ph), 7.64 (d, 2H, J = 9.4 Hz, Ph), 7.48 - 7.53 (m, 3H, Ph), 7.72 - 7.75 (m, 2H, Ph), 8.11 (s, 1H), 8.20 (s, 1H, NH). MS-ESI: 480 (M+H+), 502 (M+Na+); Anal. Calcd for C25H20F3N5O2: C, 62.63; H, 4.20; N, 14.61. Found: C,62.60; H,4.22; N,14.63.

N-(2-((E)-(4-(dimethylaminophenylimino)methyl)-3,5-dicyano-1-methyl-4-phenylcyclopenta-2,4-dienyl)-2,2,2-trifluoroacetamide (6a)

Blu-violet solid (22% yield) m.p. 215˚C - 218˚C 1H-NMR (CDCl3): δ (ppm) 1.91 (s, 3H, Me), 3.06 (s, 6H, NMe2), 6.69 (d, 2H, J = 9.0 Hz, Ph), 7.06 (s, 1H, NH), 7.35 (d, 2H, J = 9.0 Hz, Ph), 7.48 - 7.54 (m, 3H, Ph), 7.76 - 8.01 (m, 2H, Ph), 8.65 (s, 1H). MS-ESI: 464 (M+H+); Anal. Calcd for C25H20F3N5O: C, 64.79; H, 4.35; N, 15.11. Found: C, 65.00; H, 4.33; N, 15.07.

(5Z)-5-((4-dimethylamino)phenylamino)methylene)-4-methyl-2-(nitrophenyl)cyclopenta-1,3-diene-1,3-dicarbonitrile (4b)

Red-orange solid (23% yield) m.p. 280˚C - 282˚C 1H-NMR (CDCl3): δ (ppm) 2.48 (s, 3H, Me), 3.01 (s, 6H, NMe2), 6.72 (d, 2H, J = 9.0 Hz, Ph), 7.15 (d, 2H, J = 9.0 Hz, Ph), 7.91 (d, 2H, J = 8.8 Hz, Ph), 7.97 (d, 1H, J = 15.2 Hz), 8.31 (d, 2H, J = 8.8 Hz, Ph), 9.47 (d, 1H, J = 15.2 Hz, NH). MS-ESI: 396 (M-H+); Anal. Calcd for C23H19N5O2: C, 69.51; H, 4.82; N, 17.62. Found: C, 69.38; H, 4.83; N, 17.59.

(Z)-N-((2,4-dicyano-5-methyl-3-(4-nitrophenyl)-5-(2,2,2-trifluoroacetamido)cyclopenta-1,3-dien-1-yl)methylene)-4-(dimethylamino)aniline oxide (5b)

Blu solid (20% yield) m.p. 169˚C - 171˚C 1H-NMR (CDCl3): δ (ppm) 2.12 (s, 3H, Me), 3.08 (s, 6H, NMe2), 6.65 (d, 2H, J = 9.4 Hz, Ph), 7.65 (d, 2H, J = 9.4 Hz, Ph), 7.89 (d, 2H, J = 8.6 Hz, Ph), 8. 13 (s, 1H), 8.28 (s, 1H, NH), 8.37 (d, 2H, J = 8.6 Hz, Ph). MS-ESI: 525 (M+H+) Anal. Calcd for C25H19F3N6O4: C, 57.25; H, 3.65; N, 16.02. Found: C, 57.43; H, 3.66; N, 16.05.

N-(2-((E)-(4-(dimethylamino)phenylimino)methyl-3,5-dicyano-1-methyl-4-(4-nitrphenyl)cyclopenta-2,4-dienyl)-2,2,2-trifluoacetamide (6b)

Blu-violet solid (20% yield) m.p. 116˚C - 118˚C 1H-NMR (CDCl3): δ (ppm) 1.93 (s, 3H, Me), 3.08 (s, 6H, NMe2), 6.70 (d, 2H, J = 9.0 Hz, Ph), 7.37 (d, 2H, J = 9.0 Hz, Ph), 7.94 (d, 2H, J = 8.8 Hz, Ph), 8.39 (d, 2H, J = 8.8 Hz, Ph), 8.64 (s, 1H). MS-ESI: 509 (M+H+); Anal. Calcd for C25H19F3N6O3: C, 59.06; H, 3.77; N, 16.53. Found: C, 59.25; H, 3.75; N, 16.57.

(5Z)-5-((4-(dimethylamino)phenyamino)methylene)-4-methyl-2-(2,4-dinitrophenyl)cyclopenta-1,3-diene-1,3-dicarbonitrile (4c)

Red-orange solid (28% yield) m.p. 155˚C - 157˚C 1H-NMR (CDCl3): δ (ppm) 2.48 (s, 3H, Me), 2.99 (s, 6H, NMe2), 5.25 (bs, 1H, NH), 6.73 (d, 2H, J = 8.8 Hz, Ph), 7.19 (d, 2H, J = 8.8 Hz, Ph), 7.71 (d, 1H, Jo = 8.6 Hz, Ph), 8.11 (d, 1H, J = 13.6 Hz,), 8.48 (dd, 1H, Jo = 8.6 Hz, Jm = 1.6 Hz, Ph), 8.85 (d, 1H, Jm = 1.6 Hz, Ph). MS- ESI: 441 (M-H+); Anal. Calcd for C23H18N6O4: C, 62.44; H, 4.10; N, 19.00. Found: C, 62.64; H, 4.08; N, 19.02.

(Z)-N-((2,4-dicyano-5-methyl-3-(2,4-dinitrophenyl)-5-(2,2,2-trifluoroacetamido)cyclopenta-1,3-dien-1-yl)methylene)-4-(dimethyl amino)aniline oxide (5c)

Blu-violet solid (25% yield) m.p. 177˚C - 179˚C 1H-NMR (CDCl3): δ (ppm) 2.16 (s, 3H, Me), 3.07 (s, 6H, NMe2), 6.65 (d, 2H, J = 9.2 Hz, Ph), 7.64 (d, 2H, J = 9.2 Hz, Ph), 7.97 (d, 1H, Jo = 8.4 Hz, Ph), 8.04 (s, 1H), 8.63 - 8.66 (m, 2H, NH, Ph), 9.17 (d, 1H, Jm = 2.0 Hz, Ph). 13C-NMR (CDCl3): δ (ppm) 19.45, 40.24, 68.60, 111.26, 112.09, 112.18, 114.00, 116.63, 119.29, 121.14, 122.93, 124.545, 129.15, 131.05, 133.71, 136.11, 146.86, 147.17, 149.44, 152.73, 153.92, 156.70. MS-ESI: 592 (M+Na), 568 (M-H+); Anal. Calcd for C25H18F3 N7O6: C, 52.73; H, 3.19; N, 17.22. Found: C, 52.90; H, 3.21; N, 17.27.

N-(2-((E)-(4-(dimethylamino)phenylimino)methyl)-3,5-dicyano-1-methyl-4-(2,4-dinitrophenyl)cyclopenta-2,4-dienyl)-2,2,2-trifluoroacetamide (6c)

Blu solid (24% yield) m.p. 110˚C - 112˚C 1H-NMR (CDCl3): δ (ppm) 1.97 (s, 3H, Me), 3.08 (s, 6H, NMe2), 6.70 (d, 2H, J = 9.0 Hz, Ph), 7.36 (d, 2H, J = 9.0 Hz, Ph), 7.96 (d, 1H, Jo = 8.0 Hz, Ph), 8.56 (s, 1H), 8.67 (dd, 1H, Jo = 8.0 Hz, Jm = 2.0 Hz, Ph), 9.20 (d, 1H, Jm = 2.0 Hz, Ph). 13C-NMR (CDCl3): δ (ppm) 23.04, 29.66, 40.25, 67.96, 111.82, 112.09, 114.07, 120.31, 121.16, 124.83, 129.07, 131.27, 133.72, 137.44, 140.13, 146.91, 149.06, 149.44, 152.13, 158.98, 166.58. MS-E SI: 576 (M+Na), 552 (M-H+); Anal. Calcd for C25H18F3N7O5: C, 54.25; H, 3.28; N, 17.72. Found: C, 54.12; H, 3.29; N, 17.66.

(5Z)-5-((4-(dimethylamino)phenylamino)methylene)2-(4-methoxyphenyl)-4-methylcyclopenta-1,3-diene-1,3-dicarbonitrile (4d)

Red-orange solid (27% yield) m.p. 215˚C - 218˚C 1H-NMR (CDCl3): δ (ppm) 2.45 (s, 3H, Me), 2.99 (s, 6H, NMe2), 3.84 (s, 3H, OMe), 6.72 (d, 2H, J = 8.8 Hz, Ph), 6.99 (d, 2H, J = 8.8 Hz, Ph), 7.12 (d, 2H, J = 8.8 Hz, Ph), 7.74 (d, 2H, J = 8.8 Hz, Ph), 7.85 (d, 1H, J = 14.8 Hz), 9.22 (d, 1H, J = 14.8 Hz, NH). MS-ESI: 383 (M+H+); Anal. Calcd for C24H22N4O: C, 75.37; H, 5.80; N, 14.65. Found: C, 75.50; H, 5.78; N, 14.68.

(Z)-N-((2,4-dicyano-5-methyl-3-(4-methoxyphenyl)-5-(2,2,2-trifluoroacetamido)cyclopenta-1,3-dien-1yl)methylene)-4-(dimethylamino)aniline oxide (5d)

Blu-violet solid (18% yield) m.p. 201˚C - 203˚C 1H-NMR (CDCl3): δ (ppm) 2.09 (s, 3H, Me), 3.06 (s, 6H, NMe2), 3.85 (s, 3H, OMe), 6.65 (d, 2H, J = 8.8 Hz, Ph), 7.01 (d, 2H, J = 8.8 Hz, Ph), 7.63 (d, 2H, J = 8.8 Hz, Ph), 7.73 (d, 2H, J = 8.8 Hz, Ph), 8.01 (s, 1H), 8.23 (s, 1H, NH). MS-ESI: 510 (M+H+); Anal. Calcd for C26H22 F3N5O3: C, 61.29; H, 4.35; N, 13.75. Found: C, 61.45; H, 4.36; N, 13.71.

N-(2-((E)-(4-(dimethylamino)phenylimino)methyl-3,5-dicyano-4-(4-methoxyhenyl)-1-methylcyclopenta-2,4-dienyl)-2,2,2-trifluoro acetamide (6d)

Blu-violet solid (20% yield) m.p. 235˚C - 240˚C 1H-NMR (CDCl3): δ (ppm) 1.89 (s, 3H, Me), 3.06 (s, 6H, NMe2), 3.86 (s, 3H, OMe), 6.69 (d, 2H, J = 8.8 Hz, Ph), 7.01 - 7.05 (m, 3H, NH, Ph), 7.35 (d, 2H, J = 9.0 Hz, Ph), 7.79 (d, 2H, J = 9.0 Hz, Ph), 8.64 (s, 1H). MS-ESI: 516 (M+Na); Anal. Calcd for C26H22F3N5O2: C, 63.28; H, 4.49; N, 14.19. Found: C, 63.47; H, 4.47; N, 14.22.

2.4. RX Crystallography Data

Single crystals of 3b, 4a and 5a were submitted to X-ray data collection by using a Siemens P4 four-circle or an Oxford-Diffraction Xcalibur Sapphire 3 diffractometer. The structures were solved by direct methods implemented in SHELXS-97 program [11] . The refinements were carried out by full-matrix anisotropic least- squares on F2 for all reflections for non-H atoms by means of the SHELXL-97 program [11] . Crystallographic data for the structure in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC 1416382 (3b), CCDC 995914 (4a), CCDC 995915 (5a). Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, CambridgeCB2 1EZ, UK; (fax: + 44 (0) 1223 336 033; or e-mail: deposit@ccdc.cam.ac.uk).

Crystal data for 3b: C22H20N4O4 (CCDC 1416382): MW = 404.42, triclinic, space group P-1, a = 7.6387 (6) Å, b = 16.6184 (12) Å, c = 17.7794 (13) Å, α = 112.298 (7), β = 94.328 (6), γ = 92.519 (6)˚, V = 2075.9 (3) Å3, Z = 4, Dc = 1.294 mg/m3, F (000) = 848, crystal dimension 0.3_0.1_0.1 mm, radiation, MoKα (λ = 0.71073 Å), 9355 intensity data were collected at 293(2) K, employing ω/2θ scanning technique, in the range of −10h9, −20k19, −24l23; the structure was solved by a direct method, all non-hydrogen atoms were refined anisotropically from 2585 observed reflections by a full-matrix least-squares technique. R = 0.0467 [I > 2σ(I)] and wR2 (all data) = 0.1012

Crystal data for 4a: C23H20N4(CCDC 995914): MW = 352.43, monoclinic, space group P21/n, a = 8.3817 (4) Å, b = 12.9420 (7) Å, c = 17.4334 (12) Å, α = 90, β = 98.704 (5), γ = 90˚, V = 1869.3 (1) Å3, Z = 4, Dc = 1.252 mg/m3, F (000) = 744, crystal dimension 0.4_0.3_0.1 mm, radiation, MoKα (λ = 0.71073 Å), 4310 intensity data were collected at 293(2) K, employing ω/2θ scanning technique, in the range of −10h8, −16k16, −22l15; the structure was solved by a direct method, all non-hydrogen atoms were refined anisotropically from 1344 observed reflections by a full-matrix least-squares technique. R = 0.0426 [I > 2σ(I)] and wR2 (all data) = 0.0873

Crystal data for 5a: C25H20F3N5O2・C6D6(CCDC 995915): MW = 479.46, monoclinic, space group P21/a, a = 11.832 (1) Å, b = 13.5134 (9) Å, c = 14.934 (2) Å, α = 90, β = 95.522 (2), γ = 90˚, V = 2376.7 (4) Å3, Z = 4, Dc = 1.34 mg/mm3, F (000) = 992, crystal dimension 0.3_0.15_0.10 mm, radiation, MoKα (λ = 0.71073 Å), 5426 intensity data were collected at 293(2) K, employing ω/2θ scanning technique, in the range of −13h15, −18k18, −18l17; the structure was solved by a direct method, all non-hydrogen were refined anisotropically from 1703 observed reflections by a full-matrix least-squares technique. R = 0.0941 [I > 2σ(I)] and wR2 (all data) = 0.1829.

3. Result and Discussion

Hence, when dienes 1a-d (0.1 mmol) were left to react with N,N-dimethyl-4-nitrosoaniline (0.12 mmol) in CH2Cl2 at room temperature for 5 - 7 days a new unexpected compound we observed. This product was also observed when the same reaction mixture was heated at 60˚C for 7 h. The crude reaction mixture was purified by column chromatography (ethyl acetate/petroleum ether 1/4) to give starting material and compounds 3a-d (Scheme 1).

The structure of compound 3b was established by X-ray analysis (Figure 2), whereas allowed MS/ESI and 1H-NMR and 13C-NMR data were sufficient to establish, by comparison, the structures of derivatives 3a, 3c and 3d.

The reaction conditions were optimized to provide compounds 3a-d in highest yields. A solution of 1a-d (0.1 mmol) and 2 (0.12 mmol) in CH2Cl2 was heated under MW (150 W) for 90 minutes. In alternative, heating the same mixture in an oil bath for 7 hours at 60˚C gave desired 3a-d in similar high yields. We have verified that increasing the temperature did not increase the yield due, which we explained considering the thermolability of the compounds 3a-d.

In order to understand the effect of the temperature on product distribution, a new set of experiments was also performed. When a mixture of dienes 1a-d (0.1 mmol) and N,N-dimethyl-4-nitrosoaniline 2 (0.12 mmol) neat were heating under MW irradiation (150 W) at 150˚C for 15 minutes, the tlc (ethyl acetate/petroleum ether 1/4) and 1H-NMR spectra of the crude reaction mixture indicated complete conversion of the starting material and appearance of compounds 4a-d, 5a-d and 6a-d (Scheme 2). The reaction products were isolated by column chromatography (ethyl acetate/petroleum ether 1/4) and further characterised via NMR spectroscopy and X-ray analysis.

RX analysis (Figure 3, Figure 4) allowed us to assign the structure of compounds 4a and 5a.

The Z configuration of compound 4a was also confirmed by NMR-NOESY experiments, which showed correlation between the 4-methyl group at 2.46 ppm and the CH group at 7.89 ppm. It is to be noted that 4a did not rearrange to the corresponding E-isomer upon UV-VIS irradiation at 440 nm.

The structure of other 4, 5 and 6 analogues was assigned by comparison of their 1H-NMR data (Table 1).

The analysis of the chemical shifts indicated very similar trend of the C-methyl group and the CH-N signals along the three series of compounds.

Also analysis of the MS/ESI data (molecular ion value and ms/ms fragmentation) confirms the assigned structure.

The medium basicity (due the presence of nitrosoamine) is a crucial parameter for the Ehrlich-Sachs reaction. In fact compounds 1a-d (0.1 mmmol in CH2Cl2) does not react with nitrosobenzene (0.12 mmmol) in the absence of base and under MW irradiation (solvent free) gave no conversion to corresponding compounds 4.

Conversely, in the presence of triethylamine (0.12 mmmol) the corresponding aniline oxide was obtained from compounds 1b,d (0.1 mmmol in CH2Cl2) and nitrosobenzene, (0.12 mmmol), as confirmed by MS/ESI data and 1H-NMR spectra: the chemical shifts of the methyl group (2.15 ppm for NO2 derivative and 2.11 ppm for OMe derivative) and those of the CH-N proton (8.18 ppm and 8.15 ppm respectively for NO2 and OMe derivatives) are diagnostic for the assignement of the structure. In addition compounds 5 (and 6 in trace) were obtained from 1 (0.1 mmmol in CH2Cl2) and 2 (0.12 mmmol) and trimethylamine (0.12 mmmol) without heating.

Fulvenes requires higher temperatures: 4a-d together with 5a-d were also obtained by heating of 1a-d (0.1 mmol) and 2 (0.12 mmol) at 100˚C in oil bath, solvent free, for 3 hours.

The formation of 3a-d may be accounted by the following mechanisms (Scheme 3).

We envisaged that, following an initial hetero Diels-Alder reaction [2] , deprotonation of NHCOCF3 group lead to formation of an open intermediate which rearranged to a dihydrofuran. Finally, the hydrolysis (the

reaction is made in non-anhydrous conditions) of the trifluoroacetamidate group gave the observed compounds 3a-d.

Scheme 1. 1a-d (0.1 mmol) and 2 (0.12 mmol) in CH2Cl2 (3 ml) at RT for 5 - 7 days or T = 60˚C in bath oil for 7 h, or heating in MW 150 W for 90 minutes.

Scheme 2. 1a-d (0.1 mmol) and 2 (0.12 mmol) in MW at T = 150˚C, 150W for 15’ solvent free or heating in oil bath at T = 100˚C for 3 h solvent free.

Scheme 3. Proposed mechanism for the formation of compounds 3a-d.

Crystal structure of compound 3b (CCDC1416382). Ellipsoids enclose 50% probability. Crystal structure of compound 4a (CCDC995914). Ellipsoids enclose 50% probability Crystal structure of compound 5a (CCDC995915). Ellipsoids enclose 50% probability Selected proton NMR of compounds 4a-d, 5a-d and 6a-d
R
4a-d5a-d6a-d
MeCH-NMeCH-NMeCH-N
Phenyl7.892.462.118.111.918.65
4-NO2Phenyl7.972.482.128.131.938.64
2,4diNO2Phenyl8.112.482.168.041.978.56
4-OMePhenyl7.852.452.098.011.898.64

The formation of the imines 6a-d and nitrones 5a-d could be explained by an Ehrlich-Sachs condensation mechanism involving nitroso group and acidic methyl group, followed by partial oxidation to 5 by the excess of reagent [3] .

The formation of fulvenes can be hypothesized as deriving from 6a-d considering that nitrosobenzene, in pre- sence of carbanions with good leaving groups gave N-oxides [3] . In this case, the acidic NH was deprotonated to an N-anion able to carry a nucleophilic attack to the electrophilic nitrosoaniline. In this context, the fulvene behaved as a leaving group generating compounds 4a-d and trifluoroacetyldiazene-oxide 7 (Scheme 4).

We have carried out some mechanistic studies that support this interpretation. For example, heating compounds 6a-d in the presence of N,N-dimethyl-4-nitrosoaniline 2, under neat conditions, provided fulvenes which were characterised by t.l.c. mass spectrometry and 1H-NMR. In addition, the presence of trifluoroacetyl-

Scheme 4. Proposed reaction for the formation of compounds 4a-d.

diazene-oxide 7 could be evidenced in the crude mixture [12] .

4. Conclusion

In conclusion, we have shown that the reaction of compounds 1 and 2 could be in two diverse directions providing either substituted dihydrofuran or fulvenes depending upon conditions applied. The increase in temperature does not lead to the cycloaddition reaction, but a different mechanism occurs. The interest on synthetic methodologies leading to 2,5-dihydrofuran and imino-2,5-dihydrofuran derivatives [13] is very considerable. These structures are subunit of several bioactive natural and synthetic products [14] [15] . Fulvenes have high relevance as synthons [16] [17] and materials [18] - [24] . This report will provide a fast and easy protocol to execute the preparation of the abovementioned heterocycles cores.

Acknowledgements

The work was financially supported by the funds of University of Siena. We would like to thank Dr. Sara Draghi for ESI-MS analysis, Dr. Iacopo Barbetti for laboratory experimental assistance and the Centro di Analisi e Determinazioni Strutturali of the University of Siena for X-ray data collection.

Cite this paper

Stefania Fusi,Donato Donati,Fabio Ponticelli, (2016) Reaction of Arylnitroso Derivatives: Synthesis of Arylimino 2,5-Dihydrofuran and Arylamino Fulvenes Derivatives. International Journal of Organic Chemistry,06,147-155. doi: 10.4236/ijoc.2016.62016

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