Reaction of 1-aryl-2-methylenecyclopropanes with rhodium(I) complexes leading to ring opening isomerization and π co-ordination of the C[double bond, length half m-dash]C double bond

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Kohtaro Osakada, Hisami Takimoto and Takakazu Yamamoto


Abstract

1-Aryl-2-methylenecyclopropanes reacted with [RhCl(PPh3)3] at 50 °C to give [RhCl(η4-CH2[double bond, length half m-dash]CArCH[double bond, length half m-dash]CH2)(PPh3)2] (Ar = C6H5 1a, C6H4F-p 1b, C6H4Me-p 1c or C6H4OMe-p 1d) via ring opening isomerization of the substrate and its subsequent co-ordination to Rh. The diene-co-ordinated rhodium complexes have been characterized by X-ray crystallography and NMR spectroscopy. Similar reaction at 0 °C afforded the rhodium(I) complexes with π-co-ordinated 1-aryl-2-methylenecyclopropane, [RhCl(η2-CH2[double bond, length half m-dash][upper bond 1 start]CCH2C[upper bond 1 end]HAr)(PPh3)2] (Ar = C6H5 2a, C6H4F-p 2b, C6H4Me-p 2c or C6H4OMe-p 2d). Exchange of the ligand of 2a with added 1-aryl-2-methylenecyclopropanes occurs reversibly at 30–45 °C with the thermodynamic parameters of the reactions 2a + CH2[double bond, length half m-dash][upper bond 1 start]CCH2C[upper bond 1 end]HC6H4X-p ⇄ 2b (or 2c) + CH2[double bond, length half m-dash][upper bond 1 start]CCH2C[upper bond 1 end]HC6H5 being ΔH[hair space]° = –10.3 kJ mol–1 and ΔS[hair space]° = –32 J K–1 mol–1 for X = F and ΔH[hair space]° = 2.2 kJ mol–1 and ΔS[hair space]° = –2.6 J K–1 mol–1 for X = Me, respectively, at 298 K. The structure of a PEt3 co-ordinated analog, [RhCl(η2-CH2[double bond, length half m-dash][upper bond 1 start]CCH2C[upper bond 1 end]HC6H4Me-p)(PEt3)2] 3c, has been determined by X-ray crystallography. The reaction of 1-methylene-2-phenylcyclopropane with [RhCl(PPh3)3] at 25 °C gave a mixture of 1a and 2a. Heating of a benzene solution of 2a at 50 °C turned it into 1a in low yield (<7%), while the reactions of 1-methylene-2-phenylcyclopropane with 2a at the same temperature gave 1a (10%) and 2-phenylbuta-1,3-diene (14%). The amounts of the products formed via ring opening isomerization in these reactions are much smaller than those in the reaction of 1-methylene-2-phenylcyclopropane with [RhCl(PPh3)3] at 50 °C.


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