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    • 6. 发明申请
    • Alcohol Oxidation Catalyst and Method of Synthesizing the Same
    • 醇氧化催化剂及其合成方法
    • US20070232838A1
    • 2007-10-04
    • US11570756
    • 2005-06-24
    • Yoshiharu IwabuchiMasatoshi ShibuyaMasaki Tomizawa
    • Yoshiharu IwabuchiMasatoshi ShibuyaMasaki Tomizawa
    • C07D487/00B01J31/02C07C29/00
    • C07D471/08B01J31/006B01J31/0235B01J31/0237B01J2231/70C07C45/29
    • An organic oxidation catalyst for alcohols which is environmentally less harmful and with which efficient oxidation can be conducted. The oxidation catalyst for alcohols is a 1-alkyl-2-azadamantan-N-oxyl which has a nitroxyl group incorporated in the adamantane skeleton and was synthesized from as a base material a bicyclic compound obtained by the Grob-type ring-opening reaction of 1,3-adamantanediol. Due to the nitroxyl group on the adamantane skeleton, the α-position hydrogen is stabilized based on Bredt's rule and the stability of the oxoammonium group generated by the oxidation thereof is ensured. Compared to TEMPO, which is a conventional oxidation catalyst, this catalyst is reduced in steric hindrance and is usable in a wide range of reaction fields. Because of this, not only a primary alcohol but a secondary alcohol having a sterically complicated structure, which has been difficult to oxidize with TEMPO, can be oxidized at a high efficiency.
    • 用于醇的有机氧化催化剂,其对环境无害且能够进行有效的氧化。 醇的氧化催化剂是在金刚烷骨架中具有硝酰基的1-烷基-2-氮杂金刚烷-N-氧基,其作为基材通过由Grob型开环反应获得的双环化合物合成, 1,3-金刚烷二醇 由于金刚烷骨架上的硝酰基,基于Bredt规则使α位氢稳定,并且确保了通过其氧化产生的氧代铵基团的稳定性。 与作为常规氧化催化剂的TEMPO相比,该催化剂的空间位阻减小,可用于广泛的反应领域。 因此,不仅可以高效地氧化难以用TEMPO氧化的伯醇和具有空间复杂结构的仲醇。