A convenient synthesis of γ-functionalized cyclopentenones

  1. Nour Lahmar1,
  2. Taïcir Ben Ayed1,
  3. Moncef Bellassoued2 and
  4. Hassen Amri1

1Laboratoire de Chimie Organique & Organométallique, Faculté des Sciences, Campus Universitaire 2092-Tunis, Tunisie
2Laboratoire de Synthèse Organométallique, 5 mail Gay-Lussac, Neuville sur Oise, 95031 Cergy-Pontoise Cedex, France

  1. Author email
  2. Corresponding author email

Beilstein J. Org. Chem. 2005, 1, No. 11. doi:10.1186/1860-5397-1-11
Received 20 Jun 2005, Accepted 07 Oct 2005, Published 07 Oct 2005


The synthesis of γ-functionalized cyclopentenones was carried out in a few steps, starting firstly with the preparation of nitroketonic intermediates 2, which were readily transformed into 1,4-diketones using the Nef conversion. The intramolecular cyclization of the γ-diketones 3 in a basic medium, led to the functionalized cyclopentenones 4.

Keywords: Nef reaction; conjugated addition; nitroalkanes; 1,4-diketones; functionalized cyclopentenones


The cyclopentenones are considered as an important class of compounds because they are present in a large variety of natural products and in many important biologically active compounds [1-6] such as prostanoids, jasmonoids, rethrolones, methylenomycins and allylrethrones. In this paper, we wish to describe a new synthetic procedure for the preparation of γ-functionalized cyclopentenones 4 via a conjugate addition of nitroalkanes to α,β-unsaturated ketones 1 leading to the nitroalkanes derivatives 2 which may be converted into their γ-diketone homologues 3 using Nef reaction. The intramolecular cyclization of 1,4-diketones 3 led to the corresponding cyclopentenones 4.

Results and discussion

As previously reported, the 1,4-addition of primary nitroalkanes [7-12] to functionalized α,β-unsaturated ketones was considered as an appropriate method to prepare multifunctional nitroketonic compounds. These intermediates are important in organic synthesis because the nitro group can be converted into other useful groups such as amines or carbonyls.[13,14] Treatment of α,β-unsaturated ketones 1[15] with primary nitroalkanes was achieved by refluxing the mixture at 50°C in THF using sodium methoxide as base (Scheme 1), resulting in full conversion and yielding the Michael adducts 2 (Table 1).


Scheme 1: Synthesis of nitroalkanes derivatives 2 and their corresponding 1,4-diketones 3.

Table 1: Synthesis of nitroalkanes derivatives 2 and their corresponding 1,4-diketones 3

A R R1 1,4-Nitroketone Yield (%) 1,4-Diketone Yield (%)
CO2Me Me H 2a 65 3a 67
CO2Et Me H 2b 62 3a 64*
CH2CO2Et Me H 2c 61 3c 53*
Ph Me H 2d 76 3d 68
CO2Me Ph H 2e 68 3e 64
CO2Me Me Me 2f 61 3f 63
CO2Et Me Me 2g 62 3f 62*
CH2CO2Et Me Me 2h 61 3h 48*
Ph Me Me 2i 76 3i 65
CO2Me Ph Me 2j 70 3j 63

*This compound undergoes transesterification reaction.

Various synthetic methods were developed to obtain 1,4-diketones [16-20] since these compounds were valuable intermediates in the synthesis of cyclopentenone ring system. Obviously the most straightforward route was the Nef reaction. The transformation of the nitro derivatives to carbonyls by the formation of the nitronate anion in the presence of sodium methoxide followed by its addition to concentrated sulfuric acid at -50°C, allowed the formation of the 1,4-diketones 3 in fair to good yields (Table 1).

During recent years, some cyclopentenones derivatives were known to exhibit biological and pharmaceutical properties and have been widely studied [21-23]. In order to contribute to the synthesis of this family of products, we present in this work a strategy of preparation of a new γ-functionalized cyclopentenones 4. Thus, we showed that intramolecular cyclization of the functionalized 1,4-diketones 3 could be conducted in the presence of anhydrous potassium carbonate (K2CO3) in the refluxing methanol to afford the pure cyclopentenones 4 with satisfactory yields (Table 2, Scheme 2).


Scheme 2: γ-Functionalized cyclopentenones 4.

Table 2: γ-Functionalized cyclopentenones 4 prepared

Cyclopentenones A R R1 Time (min) Yield (%)
4d Ph Me H 90 72
4e CO2Me Ph H 75 70
4f CO2Me Me Me 80 65
4i Ph Me Me 60 85
4j CO2Me Ph Me 65 73


A convenient procedure has been developed for the synthesis of γ-functionalized cyclopentenones 4 using the reaction between nitroalkanes and α,β-unsaturated ketones 1 to afford γ-nitroketonic intermediates 2 which may be converted into their γ-diketones homologues 3 using Nef reaction. The intramolecular cyclization of diketones 3 leads to the corresponding cyclopentenones 4. The easy workup procedure and short reaction steps, impart greater merit of this methodology over those existing.


All reactions are carried out under a nitrogen atmosphere. Unless otherwise noted, all products are purified before use. 1H-NMR spectra (300 MHz) and 13C NMR spectra (75 MHz) were recorded on Bruker AC 300 MHz spectrophotometers using CDCl3 as solvent. Chemical shifts (δ) are given from TMS (0 ppm) as internal standard for 1H-NMR and CDCl3 (77.0 ppm) for 13C NMR. Flash chromatography was done on Merck grade 60 silica gel (230–400 mesh) using mixtures of hexane and ethyl acetate as eluent.

Synthesis of nitroketones (2): General procedure

To a mixture of nitroalkanes (32 mmol) and sodium methoxide (32 mmol) in anhydrous THF (20 mL) was added vinylketone 1 (a-j) (8 mmol), the solution was stirred for 13 h at 50°C, the mixture was treated with H2O and extracted with Et2O (3 × 20 mL). The organic layer was washed with brine and dried (MgSO4). The solvent was removed to leave an oil which was purified by column chromatography on silica gel.

3-Acetyl-5-nitrohexanoic acid methyl ester (2a)

Purified by column chromatography (hexane/AcOEt, 7/3). 1H NMR (300 MHz, CDCl3) δ 1.55 (d, 3H, J = 6.7 Hz), 2.29 (s, 3H), 2.37–2.79 (2 m, 4 H), 2.92 (m, 1H), 3.67 (s, 3H), 4.55 (m, 1H); 13C NMR (75 MHz, CDCl3) δ 19.8, 29.8, 34.4, 36.2, 44.7, 52.0, 81.6, 171.4, 208.4. HRMS Calcd C9H15NO5: 217.0950. Found: 217.0932.

Preparation of functionalized 1,4-diketones (3): General procedure

At the solution of sodium (7.5 mmol) in 15 mL of methanol, was added at room temperature the nitro intermediate 2 (5 mmol). After one hour, a solution of H2SO4 (3 mL) in 15 mL of methanol at -50°C was added. The mixture was treated with H2O, the methanol was evaporated, and the residue was extracted with dichloromethane. The organic layer was washed by a solution of NaOH 1% and a solution of NaCl and dried (MgSO4). The solvent was removed to leave oil, which was purified by column chromatography on silica gel.

3-Acetyl-5-oxohexanoic acid methyl ester (3a)

Purified by column chromatography (hexane/AcOEt, 7/3). 1H NMR (300 MHz, CDCl3) δ 2.15 (s, 3H), 2.28 (s, 3H), 2.43; 2.65 (ABd, 2H, JAB = 16.5 Hz, JA-H = 7 Hz, JB-H = 6.6 Hz), 2.60; 2.93 (ABd, 2H, JAB = 18.1 Hz, JA-H = 8 Hz, JB-H = 5.5 Hz), 3.36 (m, 1H), 3.67 (s, 3H); 13C NMR (75 MHz, CDCl3) δ 29.2, 29.8, 35.0, 42.9, 44.4, 51.9, 172.0, 206.2, 209.5. HRMS Calcd C9H14O4: 186.0892. Found: 186.0877.

Preparation of γ-functionalized cyclopentenones (4): General procedure

To a solution of 1,4-diketone 3 (5 mmol) in MeOH (10 mL) was added 1 equivalent of K2CO3, the mixture was bring to reflux during one hour. After workup, the product 4 was purified by column chromatography on silica gel (EtOAc/hexane).

4-Benzyl-3-methylcyclopent-2-enone (4d)

Purified by column chromatography (hexane/AcOEt, 8/2). 1H NMR (300 MHz, CDCl3) δ 2.09 (s, 3H), 2.26–2.59 (m, 2H), 2.71 (m, 1H), 3.21 (m, 2H), 5.92 (s, 1H), 7.17–7.28 (m, 5H); 13C NMR (75 MHz, CDCl3) δ 19.4, 37.0, 39.0, 48.0, 126.3, 128.4, 128.8, 129.8, 139.6, 177.6, 211.0. HRMS Calcd C13H14O: 186.1045. Found: 186.1029


  1. Mikolajczyk, M.; Grzejszczak, S.; Midura, W.; Zatorski, A. Phosphorus Sulfur Relat. Elem. 1983, 18, 175–178.
    Return to citation in text: [1]
  2. Romanet, R. F.; Schlessinger, R. H. J. Am. Chem. Soc. 1974, 96, 3701–3702. doi:10.1021/ja00818a082
    Return to citation in text: [1]
  3. Ballini, R. Synthesis 1993, 687–688. doi:10.1055/s-1993-25922
    Return to citation in text: [1]
  4. Mikolajczyk, M.; Mikina, M.; Zurawinski, R. Pure Appl. Chem. 1999, 71, 473–480.
    Return to citation in text: [1]
  5. Mikolajczyk, M.; Grzejszczak, S.; Lyzwa, P. Tetrahedron Lett. 1982, 23, 2237–2240. doi:10.1016/S0040-4039(00)87310-4
    Return to citation in text: [1]
  6. Rezgui, F.; Amri, H.; El Gaïed, M. M. Tetrahedron 2003, 59, 1369–1380. doi:10.1016/S0040-4020(03)00035-8
    Return to citation in text: [1]
  7. Ballini, R.; Bosica, G.; Petrelli, L.; Petrini, M. Synthesis 1999, 1236–1240. doi:10.1055/s-1999-3533
    Return to citation in text: [1]
  8. Ballini, R.; Bosica, G.; Fiorini, D.; Righi, P. Synthesis 2002, 681–685. doi:10.1055/s-2002-23548
    Return to citation in text: [1]
  9. Nef, J. U. Liebigs Ann. Chem. 1894, 280, 263–291.
    Return to citation in text: [1]
  10. Ballini, R.; Bosica, G.; Livi, D. Synthesis 2001, 1519–1522. doi:10.1055/s-2001-16098
    Return to citation in text: [1]
  11. Chamakh, A.; M'hirsi, M.; Villiéras, J.; Lebreton, J.; Amri, H. Synthesis 2000, 2, 295–299. doi:10.1055/s-2000-6257
    Return to citation in text: [1]
  12. Hbaïeb, S.; Amri, H. J. Soc. Chim. Tunis. 2000, 671–681.
    Return to citation in text: [1]
  13. Seebach, D.; Colvin, E. W.; Lehr, F.; Weller, T. Chimia 1979, 33, 1–18.
    Return to citation in text: [1]
  14. Kende, A. S.; Mendoza, J. S. Tetrahedron Lett. 1991, 32, 1699–1702. doi:10.1016/S0040-4039(00)74307-3
    Return to citation in text: [1]
  15. Ben Ayed, T.; Amri, H. Synth. Commun. 1995, 25, 3813–3819.
    Return to citation in text: [1]
  16. Mc murry, J. E.; Melton, J. J. Am. Chem. Soc. 1971, 93, 5309–5311. doi:10.1021/ja00749a086
    Return to citation in text: [1]
  17. Mc Murry, J. E.; Melton, J. J. Org. Chem. 1973, 38, 4367–4373. doi:10.1021/jo00965a004
    Return to citation in text: [1]
  18. Bartlett, P. A.; Green, F. R., III; Webb, T. R. Tetrahedron Lett. 1977, 331–334. doi:10.1016/S0040-4039(01)92629-2
    Return to citation in text: [1]
  19. Bellassoued, M.; Dardoise, F.; Gaudemar, M. J. Organomet. Chem. 1979, 177, 35–38. doi:10.1016/S0022-328X(00)92329-5
    Return to citation in text: [1]
  20. Ballini, R.; Bartoli, G. Synthesis 1993, 965–967. doi:10.1055/s-1993-25981
    Return to citation in text: [1]
  21. Pohmakotr, M.; Chancharunee, S. Tetrahedron Lett. 1984, 25, 4141–4144. doi:10.1016/S0040-4039(01)90204-7
    Return to citation in text: [1]
  22. Welch, S. C.; Assercq, J. M.; Loh, J. P.; Glase, S. A. J. Org. Chem. 1987, 52, 1440–1450. doi:10.1021/jo00384a012
    Return to citation in text: [1]
  23. Ballini, R.; Petrini, M.; Marcantoni, E.; Rosini, G. Synthesis 1988, 231–233. doi:10.1055/s-1988-27524
    Return to citation in text: [1]

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