Aryl-substituted alkenes (ArHC=CH2) react with alkyl halides (R–X, X = Br or Cl) in the presence of a catalytic amount of [Cp2TiCl2] and nBuMgCl in Et2O to give alkylated alkenes (ArHC=CHR). This reaction proceeds regio- and stereoselectively under mild conditions to afford E-olefins. Primary and secondary alkyl bromides and secondary alkyl chlorides can be used as suitable alkylating reagents. The reactions of aliphatic alkenes, such as 1-octene and internal alkenes, were sluggish. When t-alkyl halides are employed, alkylative dimerization of alkenes proceeds exclusively to give symmetrical vic-diarylalkanes. These reactions involve addition of alkyl radicals to arylalkenes to form benzyl radicals as a carbon–carbon bond-forming step. Dimerization of thus formed benzyl radicals affords symmetrical alkanes and β-hydrogen elimination from benzyltitanocene intermediates gives alkylated alkenes. A possibility that titanocene activates alkenes as radical accepters was also proposed.

Titanocene-Catalyzed Alkylation of Aryl-Substituted Alkenes with Alkyl Halides.-It is noteworthy that in the reaction of (I) with (II) the use of i-PrMgCl instead of BuMgCl resulted in only 17% of (III). Mechanistical aspects are discussed. -(TERAO, J.; WATABE, H.; MIYAMOTO, M.; KAMBE*, N.; Bull. Chem.