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Ruthenium-Catalyzed One-Pot -Alkylation of Secondary Alcohols with Primary Alcohols
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文摘
Secondary alcohols (carbinols) react withprimary alcohols in dioxane at 80 C in the presence ofa catalytic amount of RuCl2(PPh3)3 and KOH along witha sacrificial hydrogen acceptor to afford the corresponding coupled secondary alcohols. The reaction is applicable to a wide range of aryl methyl, alkyl methyl,and cyclic carbinols, and with alkyl methyl carbinols,the alkylation took place exclusively at the less-hinderedmethyl position over -methylene and -methine.

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