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Synlett 2003(2): 0195-0198
DOI: 10.1055/s-2003-36797
LETTER
© Georg Thieme Verlag Stuttgart · New York

A Versatile Access to 1-Cyclopropyl-2-aryl-1,3,5-hexatrienes - Domino Heck-Diels-Alder Reactions of 1,3-Dicyclopropyl-1,2-propadiene [1]

Mario Knoke, Armin de Meijere*
Institut für Organische Chemie, Georg-August-Universität Göttingen, Tammannstrasse 2, 37077 Göttingen, Germany
Fax: +49(551)399475; e-Mail: ameijer1@uni-goettingen.de;
Further Information

Publication History

Received 1 November 2002
Publication Date:
22 January 2003 (online)

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Abstract

An efficient three-step synthesis of 1,3-dicyclopropyl-1,2-propadiene (4) (overall yield 68%) starting from dicyclopropyl-acetylene was developed. The allene, when coupled with several aryl iodides and aryl bromides under palladium catalysis in the presence of a reactive dienophile, was found to undergo a domino Heck-Diels-Alder reaction to yield 3-(1′-arylalkenyl)-substituted cyclohexenes 9 in moderate to good yields (36-86%).

Key words

allenes - domino reactions - palladium catalysis - cross-coupling reactions - cycloadditions

    References

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  • 1c

    Part 83: Leonov, A.; Heiner, T.; Bes, M. T.; de Meijere, A. Eur. J. Org. Chem. 2003, in press.

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12

Dimethyl 3-[(2′-Cyclopropyl-1′-phenyl)ethenyl]cyclo-hex-4-en-( E )-1,2-dicarboxylate ( 5a). Typical Procedure: A solution of 11.2 mg (50.0 µmol, 5 mol%) of palladium(II) acetate and 39.3 mg (150 µmol) of triphenylphosphine in 1 mL of anhyd DMF in a 5 mL Pyrex-screw-cap bottle is flushed with nitrogen for 10 min. A mixture of 120 mg
(1.00 mol) of 1,3-dicyclopropyl-1,2-propadiene, 245 mg (1.20 mmol) of phenyl iodide, 202 mg (2.00 mmol) of triethylamine and 288 mg (2.00 mmol) of dimethyl maleate are added and the mixture is stirred under nitrogen in the capped bottle at 100 °C for 24 h. The reaction is quenched by addition of 10 mL of water, and the mixture is extracted with diethyl ether (4 × 10 mL). The combined organic layers are washed with water (3 × 25 mL) and brine (25 mL). The solution is dried (MgSO4), the solvent removed, and the residue purified by chromatography on 60 g of silica gel [pentane-diethyl ether (10:1), R f = 0.10] to yield 293 mg (86%) of 5a. IR (KBr): ν = 2982, 2873, 1746, 1492, 1383, 1249, 1125, 1077, 953, 845, 763, 702 cm-1. 1H NMR (600 MHz, CDCl3): δ = 0.21-0.27 (m, 2 H, cPr-H), 0.56 (ddd, 3 J = 8.2, 2.4 Hz, 2 J = 0.6 Hz, 2 H, cPr-H), 1.17 (m, 1 H, cPr-H), 2.10 (m, 1 H, 6-H), 2.27 (m, 1 H, 6-H), 2.69 (dd, 3 J = 10.9, 10.1 Hz, 1 H, 2-H), 2.94 (dt, 3 J = 10.9, 5.4 Hz, 1 H, 1-H), 3.37 (ddd, 3 J = 10.1, 3.9 Hz, 4 J = 2.0 Hz, 1 H, 3-H), 3.57 (s, 3 H, OCH3), 3.60 (s, 3 H, OCH3), 4.81 (d, 3 J = 9.9 Hz, 1 H, 2′-H), 5.64 (m, 2 H, 4-H, 5-H), 7.14-7.32 (m, 5 H, Ph-H). 13C NMR (62.9 MHz, CDCl3): δ = 7.3 (CH2, cPr-C), 11.1 (CH, cPr-C), 27.2 (CH2, C-6), 42.1 (CH, C-1), 46.6 (CH, C-2), 48.5 (CH, C-3), 51.5 (CH3, OCH3), 51.9 (CH3, OCH3), 124.6 (CH, C-5), 126.7 (CH, Ph-C), 127.8 (CH, Ph-C), 129.6 (CH, C-4), 129.7 (CH, Ph-C), 135.2 (CH, C-2′), 138.6 (C quat, Ph-C), 139.2 (C quat, C-1′), 174.4 (C quat, COO), 175.1 (C quat, COO). MS (EI, 70 eV): m/z (%) = 341/340 (8/38) [M+], 309(20), 280(100), 249(39), 221(61), 205(33), 193(28), 167(29), 143(70), 128(34), 115(24), 91(43), 77(8), 59(12), 41(4). Calcd. for C21H24O4 (340.4): C, 74.09; H, 7.11. Found: C, 74.34; H, 6.94.

15

A control experiment which was carried out with the isolated hexatriene 7 and dimethyl maleate in 5 mL DMSO at 100 °C for 18 h in the absence of any base and palladium catalyst, gave the same product 5a as a mixture of diastereoisomers (2.3:1) in 36% yield.

16

All new compounds were fully characterized by spectroscopic methods (1H NMR, 13C NMR, IR, MS) and bulk purities were established for most of them by elemental analysis.

17

Typical Two-step Procedure: A solution of 11.2 mg (50.0 µmol, 5 mol%) of palladium(II) acetate and 39.3 mg (150 µmol) of triphenylphosphine in 1 mL of anhyd DMF in a 5 mL Pyrex-screw-cap bottle is flushed with nitrogen for 10 min. 120 mg (1.00 mol) of 1,3-dicyclopropyl-1,2-propadiene, 1.20 mmol of the aryl iodide and 202 mg (2.00 mmol) of triethylamine are added, and the mixture is stirred at 80 °C for 5 h. Then 2 mmol of the dienophile is added and the mixture is stirred at 100 °C for 18 h. The reaction is quenched by addition of 10 mL of water, and the mixture extracted with diethyl ether (3 × 10 mL). The combined organic layers are washed with water (2 × 25 mL) and brine (25 mL). After drying (MgSO4), the solvent is removed and the residue purified by chromatography.