首页> 外文期刊>Research on Chemical Intermediates >Design, characterization, and use of N,N-diethyl-N-sulfoethanaminium hydrogen sulfate {[Et3N-SO3H]HSO4} as a novel and highly efficient catalyst for preparation of alpha,alpha '-bis(arylidene)cycloalkanones
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Design, characterization, and use of N,N-diethyl-N-sulfoethanaminium hydrogen sulfate {[Et3N-SO3H]HSO4} as a novel and highly efficient catalyst for preparation of alpha,alpha '-bis(arylidene)cycloalkanones

机译:N,N-二乙基-N-磺基硫铵硫酸氢盐{[Et3N-SO3H] HSO4}的设计,表征和使用,作为制备α,α'-双(亚芳基)环烷酮的新型高效催化剂

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The aim of this work is to introduce a novel and attractive protic acidic ionic liquid as catalyst for organic synthesis. To achieve this aim, N,N-diethyl-N-sulfoethanaminium hydrogen sulfate {[Et3N-SO3H]HSO4} was prepared by reaction of NEt3 with ClSO3H and then with H2SO4. The novel acidic ionic liquid was identified by Fourier-transform infrared (FT-IR), H-1 nuclear magnetic resonance (NMR), C-13 NMR, and mass spectroscopies. Its catalytic activity was then examined in the cross-aldol condensation reaction of arylaldehydes with cycloalkanones under solvent-free conditions, obtaining a, alpha'-bis(arylidene)cycloalkanones in high yield after short reaction time.
机译:这项工作的目的是引入一种新颖且有吸引力的质子酸性离子液体作为有机合成的催化剂。为了实现该目的,通过使NEt 3与ClSO 3 H然后与H 2 SO 4反应来制备N,N-二乙基-N-磺基硫代硫酸铵硫酸氢盐{[Et3N-SO3H] HSO4}。通过傅立叶变换红外光谱(FT-IR),H-1核磁共振(NMR),C-13 NMR和质谱鉴定了新型酸性离子液体。然后在无溶剂条件下,在芳醛与环烷酮的交叉醇醛缩合反应中检查其催化活性,在短时间后以高收率获得α'-双(亚芳基)环烷酮。

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