应用化学 ›› 2009, Vol. 26 ›› Issue (11): 1305-1309.

• 研究论文 • 上一篇    下一篇

氮羟基邻苯二甲酰亚胺催化的α-紫罗兰酮的氧化反应

江文辉,周亚平,唐瑞仁*,李菲   

  1. (中南大学化学化工学院 长沙 410083)
  • 收稿日期:2008-10-29 修回日期:2009-02-20 出版日期:2009-11-10 发布日期:2009-11-10
  • 通讯作者: 唐瑞仁,男,博士,教授; E-mail:trr@mail.csu.edu.cn; 研究方向:有机合成

Aerobic oxidation of α-ionone catalyzed by N-hydroxyphthalimide(NHPI) combined with Co(acac)2

JIANG Wen-Hui, ZHOU Ya-Ping, TANG Rui-Ren*, LI Fei   

  1. (School of Chemistry and Chemical Engineering,Central South University,Changsha 410083)
  • Received:2008-10-29 Revised:2009-02-20 Published:2009-11-10 Online:2009-11-10

摘要:

以分子氧(O2)为氧化剂,在无溶剂条件下,研究了N-羟基邻苯二甲酰亚胺/乙酰丙酮亚钴(Ⅱ)体系对α-紫罗兰酮的催化氧化反应,分析了氧化产物,主要得到α-紫罗兰酮的烯丙位氧化产物5-氧代-α-紫罗兰酮,同时生成少量环氧α-紫罗兰酮及重排产物4-氧代-β-紫罗兰酮和环氧β-紫罗兰酮,提出了可能的反应机理,化合物的结构经IR, 1H NMR, MS和EA等手段得以表征;为了提高5-氧代-α-紫罗兰酮的选择性和催化氧化反应的转化率,优化了催化氧化反应的工艺条件:当反应温度为70 ℃,氧气压力为1.0 MPa,N-羟基邻苯二甲酰亚胺和乙酰丙酮亚钴(Ⅱ)用量分别为α-紫罗兰酮的25%和1.0%,反应10 h,5-氧代-α-紫罗兰酮的产率达53.4%,反应转化率达95.0%以上,平行实验表明,实验重复性良好。

关键词: N-羟基邻苯二甲酰亚胺, 催化氧化, α-紫罗兰酮, 5-氧代-α-紫罗兰酮

Abstract:

A practical catalytic method to oxidize α-ionone with molecular oxygen under normal pressure and temperature using N-hydroxyphthalimide (NHPI) combined with Co(acac)2 was developed, and probable catalytic mechanism was proposed. Influences of the reaction conditions on conversion of α-ionone and the selectivity of the major product (5-keto-α-ionone) were investigated, the optimal technical parameters for 5-keto-α-ionone were optimized. The results show that the primary products are 5-keto-α-ionone, epoxy-α- ionone, as well as rearrangement products 4-keto-β-ionone and epoxy-β-ionone, which are characterized by infrared spectra, proton nuclear magnetic resonance spectra, mass spectra and elemental analyzer; The yield of 5-keto-α-ionone and the conversion of α-ionone are 53.4% and 95.0%, respectively, when 25 % NHPI, 1.0% Co(acac)2 (in mole ratio) and no solvent is employed under O2 pressure for 1.0MPa and the reaction temperature at 70℃ for 10h, the procedure shows good reproducibility in the parallel experiments.

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