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An Efficient and Mild Oxidation of α-Isophorone to Ketoisophorone Catalyzed by N-Hydroxyphthalimide and Copper Chloride

机译:N-羟基邻苯二甲酰亚胺和氯化铜催化α-异佛尔酮高效轻度氧化为酮异佛尔酮

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N-hydroxyphthalimide (NHPI) and copper chloride (CuCl2) were first utilized for aerobic oxidation of α- isophorone (α-IP) to ketoisophorone (KIP) and the effects of co-catalysts, temperature, reaction time, solvent, amount of CuCl2 and pressure of oxygen were investigated extensively. NHPI/CuCl2 turned out to be highly efficient to this oxidation with up to 91.3% conversion and 81.0% selectivity under mild conditions. And various hydrocarbons including benzylic compounds, cycloalkene and its derivatives were also oxidized smoothly under optimized conditions. Moreover, the possible reaction mechanism was proposed and verified by FT-IR spectra.
机译:N-羟基邻苯二甲酰亚胺(NHPI)和氯化铜(CuCl2)首先用于将α-异佛尔酮(α-IP)有氧氧化为酮基异佛尔酮(KIP)以及助催化剂,温度,反应时间,溶剂,CuCl2量的影响对氧气的压力和压力进行了广泛的研究。事实证明,NHPI / CuCl2对这种氧化非常有效,在温和条件下的转化率高达91.3%,选择性高达81.0%。在优化的条件下,包括苄基化合物,环烯烃及其衍生物在内的各种烃类也被平滑氧化。此外,提出了可能的反应机理并通过FT-IR光谱进行了验证。

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