Abstract
Diesel or jet fuel range branched alkanes were synthesized for the first time by the combination of hydroxyalkylation-alkylation (HAA) of 2-methylfuran with hydroxyacetone and subsequent hydrodeoxygenation. Due to the electron-withdrawing effect of the hydroxyl group, the hydroxyacetone route exhibited evident advantages (higher HAA reactivity and diesel yield) over the previous acetone route.
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