日本化学会誌(化学と工業化学)
Online ISSN : 2185-0925
Print ISSN : 0369-4577
有機銅(II)塩触媒を用いたクロスカップリング反応による炭化水素の高選択的合成
政田 浩光安西 裕司菊地 成人
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1995 年 1995 巻 10 号 p. 844-847

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The cross-coupling reaction of the Grignard reagent with alkylating reactants (RBr, RI, and ROTs)was carried out in the presence of copper (II) acetate and organic copper (II) complex catalysts (0.01- 0.05 molar amount) in tetrahydrofuran. The reaction readily gave higher hydrocarbons (n-C17H36, n-C23H48, n -C26H54, n -C27H56, n -C29H60, n -C30H62, and n-C31H64 ), 1 - phenyloctadecane, and 1-cyclohexyloctadecane as the desired products in 90 99% isolated yields under mild conditons (-10-60° C, 2 -5h). In particular, copper (II) acetate was found to be much more effective than con ventional inorganic copper (II) salt catalysts (Li2CuCl4, CuX2) from the viewpoints of availability, solubility, stability, and activity.847

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